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1 Do enzymes change the nature of transition states? Mapping the transition state for general acid-base ...
2 Do enzymes change the nature of transition states? Mapping the transition state for general acid-base ...
3 Do enzymes change the nature of transition states? Mapping the transition state for general acid-base ...
4 Do enzymes change the nature of transition states? Mapping the transition state for general acid-base ...
5 Do enzymes change the nature of transition states? Mapping the transition state for general acid-base ...
6 Integrin alphaMbeta2 orchestrates and accelerates plasminogen activation and fibrinolysis by neutrophils
7 Integrin alphaMbeta2 orchestrates and accelerates plasminogen activation and fibrinolysis by neutrophils
8 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
9 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
10 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
11 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
12 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
13 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
14 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
15 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
16 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
17 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
18 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
19 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
20 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
21 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
22 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
23 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
24 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
25 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
26 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
27 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
28 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
29 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
30 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
31 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
32 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
33 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
34 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
35 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
36 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
37 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
38 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
39 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
40 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
41 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
42 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
43 Role of glycine 81 in (S)-mandelate dehydrogenase from Pseudomonas putida in substrate specificity and oxidase ...
44 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
45 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
46 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
47 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
48 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
49 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
50 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
51 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
52 Conserved and nonconserved residues in the substrate binding site of 7,8-diaminopelargonic acid synthase from ...
53 On the relationship between affinity for molecular hydrogen and the physiological directionality of ...
54 On the relationship between affinity for molecular hydrogen and the physiological directionality of ...
55 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
56 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
57 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
58 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
59 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
60 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
61 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
62 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
63 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
64 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
65 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
66 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
67 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
68 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
69 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
70 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
71 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
72 Identification of arginine residues important for the activity of Escherichia coli signal peptidase I
73 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
74 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
75 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
76 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
77 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
78 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
79 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
80 Protein engineering of pyruvate carboxylase: investigation on the function of acetyl-CoA and the quaternary ...
81 The mechanism of action of the fragile histidine triad, Fhit: isolation of a covalent adenylyl enzyme and ...
82 The mechanism of action of the fragile histidine triad, Fhit: isolation of a covalent adenylyl enzyme and ...
83 The mechanism of action of the fragile histidine triad, Fhit: isolation of a covalent adenylyl enzyme and ...
84 The mechanism of action of the fragile histidine triad, Fhit: isolation of a covalent adenylyl enzyme and ...
85 The mechanism of action of the fragile histidine triad, Fhit: isolation of a covalent adenylyl enzyme and ...
86 The mechanism of action of the fragile histidine triad, Fhit: isolation of a covalent adenylyl enzyme and ...
87 Reaction mechanism of chitobiose phosphorylase from Vibrio proteolyticus: identification of family 36 ...
88 Reaction mechanism of chitobiose phosphorylase from Vibrio proteolyticus: identification of family 36 ...
89 Reaction mechanism of chitobiose phosphorylase from Vibrio proteolyticus: identification of family 36 ...
90 Reaction mechanism of chitobiose phosphorylase from Vibrio proteolyticus: identification of family 36 ...
91 Reaction mechanism of chitobiose phosphorylase from Vibrio proteolyticus: identification of family 36 ...
92 Reaction mechanism of chitobiose phosphorylase from Vibrio proteolyticus: identification of family 36 ...
93 Defining the binding site of homotetrameric R67 dihydrofolate reductase and correlating binding enthalpy with ...
94 Defining the binding site of homotetrameric R67 dihydrofolate reductase and correlating binding enthalpy with ...
95 Defining the binding site of homotetrameric R67 dihydrofolate reductase and correlating binding enthalpy with ...
96 Defining the binding site of homotetrameric R67 dihydrofolate reductase and correlating binding enthalpy with ...
97 Defining the binding site of homotetrameric R67 dihydrofolate reductase and correlating binding enthalpy with ...
98 Defining the binding site of homotetrameric R67 dihydrofolate reductase and correlating binding enthalpy with ...
99 Defining the binding site of homotetrameric R67 dihydrofolate reductase and correlating binding enthalpy with ...
100 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
101 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
102 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
103 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
104 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
105 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
106 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
107 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
108 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
109 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
110 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
111 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
112 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
113 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
114 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
115 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
116 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
117 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
118 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
119 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
120 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
121 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
122 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
123 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
124 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
125 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
126 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
127 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
128 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
129 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
130 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
131 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
132 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
133 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
134 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
135 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
136 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
137 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
138 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
139 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
140 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
141 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
142 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
143 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
144 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
145 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
146 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
147 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
148 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
149 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
150 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
151 Probing the interactions between the folding elements early in the folding of Escherichia coli dihydrofolate ...
152 Kinetic evidence related to substrate-assisted catalysis of family 18 chitinases
153 Kinetic evidence related to substrate-assisted catalysis of family 18 chitinases
154 Kinetic evidence related to substrate-assisted catalysis of family 18 chitinases
155 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
156 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
157 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
158 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
159 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
160 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
161 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
162 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
163 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
164 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
165 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
166 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
167 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
168 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
169 Changing the metal ion selectivity of rabbit muscle enolase by mutagenesis: effects of zhe G37A and G41A ...
172 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
173 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
174 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
175 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
176 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
177 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
178 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
179 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
180 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
181 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
182 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
183 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
184 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
185 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
186 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
187 Characterization of Mycobacterium tuberculosis NAD kinase: functional analysis of the full-length enzyme by ...
188 Kinetics and comparative reactivity of human class I and class IIb histone deacetylases
189 Kinetics and comparative reactivity of human class I and class IIb histone deacetylases
190 Kinetics and comparative reactivity of human class I and class IIb histone deacetylases
191 Kinetics and comparative reactivity of human class I and class IIb histone deacetylases
192 Kinetics and comparative reactivity of human class I and class IIb histone deacetylases
193 Kinetics and comparative reactivity of human class I and class IIb histone deacetylases
194 Structural and mechanistic studies of chloride induced activation of human pancreatic alpha-amylase
195 Structural and mechanistic studies of chloride induced activation of human pancreatic alpha-amylase
196 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
197 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
198 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
199 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
200 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
201 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
202 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
203 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
204 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
205 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
206 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
207 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
208 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
209 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
210 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
211 Effects of AMP and fructose 2,6-bisphosphate on fluxes between glucose 6-phosphate and triose-phosphate in ...
212 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
213 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
214 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
215 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
216 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
217 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
218 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
219 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
220 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
221 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
222 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
223 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
224 Rates of elementary catalytic steps for different metal forms of the family II pyrophosphatase from ...
225 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
226 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
227 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
228 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
229 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
230 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
231 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
232 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
233 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
234 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
235 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
236 Peroxidase catalyzed nitration of tryptophan derivatives. Mechanism, products and comparison with chemical ...
237 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
238 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
239 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
240 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
241 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
242 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
243 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
244 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
245 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
246 Catalytic and structural contributions for glutathione-binding residues in a Delta class glutathione ...
247 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
248 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
249 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
250 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
251 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
252 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
253 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
254 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
255 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
256 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
257 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
258 A novel beta-lactamase activity from a penicillin-binding protein of Treponema pallidum and why syphilis is ...
259 Minimization of cavity size ensures protein stability and folding: structures of Phe46-replaced bovine ...
260 Minimization of cavity size ensures protein stability and folding: structures of Phe46-replaced bovine ...
261 Minimization of cavity size ensures protein stability and folding: structures of Phe46-replaced bovine ...
262 Minimization of cavity size ensures protein stability and folding: structures of Phe46-replaced bovine ...
263 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
264 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
265 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
266 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
267 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
268 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
269 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
270 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
271 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
272 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
273 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
274 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
275 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
276 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
277 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
278 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
279 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
280 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
281 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
282 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
283 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
284 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
285 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
286 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
287 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
288 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
289 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
290 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
291 Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha ...
292 Biochemical characterization of WbpA, a UDP-N-acetyl-D-glucosamine 6-dehydrogenase involved in O-antigen ...
293 Biochemical characterization of WbpA, a UDP-N-acetyl-D-glucosamine 6-dehydrogenase involved in O-antigen ...
294 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
295 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
296 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
297 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
298 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
299 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
300 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
301 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
302 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
303 Kinetic characterization of yeast pyruvate carboxylase isozyme Pyc1 and the Pyc1 mutant, C249A
304 Dihydrodipicolinate synthase (DHDPS) from Escherichia coli displays partial mixed inhibition with respect to ...
305 Dihydrodipicolinate synthase (DHDPS) from Escherichia coli displays partial mixed inhibition with respect to ...
306 Dihydrodipicolinate synthase (DHDPS) from Escherichia coli displays partial mixed inhibition with respect to ...
307 Different properties of the central and peripheral forms of human tryptophan hydroxylase
308 Different properties of the central and peripheral forms of human tryptophan hydroxylase
309 Different properties of the central and peripheral forms of human tryptophan hydroxylase
310 Different properties of the central and peripheral forms of human tryptophan hydroxylase
311 Different properties of the central and peripheral forms of human tryptophan hydroxylase
312 Different properties of the central and peripheral forms of human tryptophan hydroxylase
313 Different properties of the central and peripheral forms of human tryptophan hydroxylase
314 Different properties of the central and peripheral forms of human tryptophan hydroxylase
315 Different properties of the central and peripheral forms of human tryptophan hydroxylase
316 Different properties of the central and peripheral forms of human tryptophan hydroxylase
317 Different properties of the central and peripheral forms of human tryptophan hydroxylase
318 Different properties of the central and peripheral forms of human tryptophan hydroxylase
319 Different properties of the central and peripheral forms of human tryptophan hydroxylase
320 Different properties of the central and peripheral forms of human tryptophan hydroxylase
321 Different properties of the central and peripheral forms of human tryptophan hydroxylase
322 Different properties of the central and peripheral forms of human tryptophan hydroxylase
323 Different properties of the central and peripheral forms of human tryptophan hydroxylase
324 Different properties of the central and peripheral forms of human tryptophan hydroxylase
325 A metallo-beta-lactamase enzyme in action: crystal structures of the monozinc carbapenemase CphA and its ...
326 A metallo-beta-lactamase enzyme in action: crystal structures of the monozinc carbapenemase CphA and its ...
327 A metallo-beta-lactamase enzyme in action: crystal structures of the monozinc carbapenemase CphA and its ...
328 A metallo-beta-lactamase enzyme in action: crystal structures of the monozinc carbapenemase CphA and its ...
329 Trypanothione Synthesis in Crithidia Revisited
330 Trypanothione Synthesis in Crithidia Revisited
407 Characterization of a Novel NADP+- Dependent D-Arabitol Dehydrogenase from the Plant Pathogen Uromyces fabae
408 Characterization of a Novel NADP+- Dependent D-Arabitol Dehydrogenase from the Plant Pathogen Uromyces fabae
409 Characterization of a Novel NADP+- Dependent D-Arabitol Dehydrogenase from the Plant Pathogen Uromyces fabae
410 Characterization of a Novel NADP+- Dependent D-Arabitol Dehydrogenase from the Plant Pathogen Uromyces fabae
411 Characterization of a Novel NADP+- Dependent D-Arabitol Dehydrogenase from the Plant Pathogen Uromyces fabae
412 Characterization of a Novel NADP+- Dependent D-Arabitol Dehydrogenase from the Plant Pathogen Uromyces fabae
413 The role of active site glutamate residues in catalysis of Rhodobacter capsulatus xanthine dehydrogenase
414 The role of active site glutamate residues in catalysis of Rhodobacter capsulatus xanthine dehydrogenase
415 The role of active site glutamate residues in catalysis of Rhodobacter capsulatus xanthine dehydrogenase
416 The role of active site glutamate residues in catalysis of Rhodobacter capsulatus xanthine dehydrogenase
428 Kinetic Studies of DNA Cleavage Reactions Catalyzed by an ATP-Dependent Deoxyribonuclease on a 27-MHz ...
429 Kinetic Studies of DNA Cleavage Reactions Catalyzed by an ATP-Dependent Deoxyribonuclease on a 27-MHz ...
430 Kinetic Studies of DNA Cleavage Reactions Catalyzed by an ATP-Dependent Deoxyribonuclease on a 27-MHz ...
431 Kinetic Studies of DNA Cleavage Reactions Catalyzed by an ATP-Dependent Deoxyribonuclease on a 27-MHz ...
432 Kinetic Studies of DNA Cleavage Reactions Catalyzed by an ATP-Dependent Deoxyribonuclease on a 27-MHz ...
433 Kinetic Studies of DNA Cleavage Reactions Catalyzed by an ATP-Dependent Deoxyribonuclease on a 27-MHz ...
434 Human Carbonyl Reductase Catalyzes Reduction of 4-Oxonon-2-enal
435 Human Carbonyl Reductase Catalyzes Reduction of 4-Oxonon-2-enal
436 Human Carbonyl Reductase Catalyzes Reduction of 4-Oxonon-2-enal
437 Human Carbonyl Reductase Catalyzes Reduction of 4-Oxonon-2-enal
438 Human Carbonyl Reductase Catalyzes Reduction of 4-Oxonon-2-enal
439 Human Carbonyl Reductase Catalyzes Reduction of 4-Oxonon-2-enal
443 A novel assay method for an amino acid racemase based on circular dichroism
444 A novel assay method for an amino acid racemase based on circular dichroism
445 A novel assay method for an amino acid racemase based on circular dichroism
446 Human acetyl-coenzyme A:alpha-glucosaminide N-acetyltransferase. Kinetic characterization and mechanistic ...
447 Human acetyl-coenzyme A:alpha-glucosaminide N-acetyltransferase. Kinetic characterization and mechanistic ...
456 Role of Methionine-13 in the Catalytic Mechanism of 6-Phosphogluconate Dehydrogenase from Sheep Liver
457 Role of Methionine-13 in the Catalytic Mechanism of 6-Phosphogluconate Dehydrogenase from Sheep Liver
458 Role of Methionine-13 in the Catalytic Mechanism of 6-Phosphogluconate Dehydrogenase from Sheep Liver
459 Role of Methionine-13 in the Catalytic Mechanism of 6-Phosphogluconate Dehydrogenase from Sheep Liver
460 Role of Methionine-13 in the Catalytic Mechanism of 6-Phosphogluconate Dehydrogenase from Sheep Liver
461 Role of Methionine-13 in the Catalytic Mechanism of 6-Phosphogluconate Dehydrogenase from Sheep Liver
474 Dissection of the Steps of Phospholipase C beta 2 Activity That Are Enhanced by G beta gamma Subunits
475 Dissection of the Steps of Phospholipase C beta 2 Activity That Are Enhanced by G beta gamma Subunits
476 Dissection of the Steps of Phospholipase C beta 2 Activity That Are Enhanced by G beta gamma Subunits
477 Dissection of the Steps of Phospholipase C beta 2 Activity That Are Enhanced by G beta gamma Subunits
478 Dissection of the Steps of Phospholipase C beta 2 Activity That Are Enhanced by G beta gamma Subunits
479 Effect of cadmium on ferredoxin:NADP+ oxidoreductase activity
480 Effect of cadmium on ferredoxin:NADP+ oxidoreductase activity
481 Effect of cadmium on ferredoxin:NADP+ oxidoreductase activity
482 Effect of cadmium on ferredoxin:NADP+ oxidoreductase activity
483 Mechanistic and structural analysis of a family 31 alpha-glycosidase and its glycosyl-enzyme intermediate
484 Mechanistic and structural analysis of a family 31 alpha-glycosidase and its glycosyl-enzyme intermediate
485 Mechanistic and structural analysis of a family 31 alpha-glycosidase and its glycosyl-enzyme intermediate
486 Characterization of N-acetylneuraminic acid synthase isoenzyme 1 from Campylobacter jejuni
487 Characterization of N-acetylneuraminic acid synthase isoenzyme 1 from Campylobacter jejuni
488 Characterization of N-acetylneuraminic acid synthase isoenzyme 1 from Campylobacter jejuni
489 Characterization of N-acetylneuraminic acid synthase isoenzyme 1 from Campylobacter jejuni
490 Biophysical and kinetic analysis of wild-type and site- directed mutants of the isolated and native ...
491 Biophysical and kinetic analysis of wild-type and site- directed mutants of the isolated and native ...
492 Biophysical and kinetic analysis of wild-type and site- directed mutants of the isolated and native ...
493 Biophysical and kinetic analysis of wild-type and site- directed mutants of the isolated and native ...
494 Biophysical and kinetic analysis of wild-type and site- directed mutants of the isolated and native ...
495 Biophysical and kinetic analysis of wild-type and site- directed mutants of the isolated and native ...
496 Mechanistic differences in inhibition of ubiquinol cytochrome c reductase by the proximal Qo-site inhibitors ...
497 Mechanistic differences in inhibition of ubiquinol cytochrome c reductase by the proximal Qo-site inhibitors ...
498 Mechanistic differences in inhibition of ubiquinol cytochrome c reductase by the proximal Qo-site inhibitors ...
499 L-Pipecolic acid metabolism in human liver: L-alpha-aminoadipate delta-semialdehyde oxidoreductase
500 L-Pipecolic acid metabolism in human liver: L-alpha-aminoadipate delta-semialdehyde oxidoreductase
513 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
514 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
515 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
516 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
517 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
518 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
519 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
520 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
521 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
522 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
523 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
524 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
525 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
526 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
527 Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein ...
528 Amine-synthesizing enzyme N-substituted formamide deformylase: screening, purification, characterization, and ...
529 Amine-synthesizing enzyme N-substituted formamide deformylase: screening, purification, characterization, and ...
530 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
531 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
532 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
533 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
534 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
535 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
536 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
537 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
538 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
539 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
540 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
541 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
542 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
543 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
544 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
545 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
546 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
547 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
548 Mutational analysis of peptidyl carrier protein and acyl carrier protein synthase unveils residues involved in ...
557 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
558 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
559 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
560 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
561 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
562 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
563 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
564 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
565 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
566 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
567 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
568 Hexose-6-phosphate dehydrogenase determines the reaction direction of 11beta-hydroxysteroid dehydrogenase type ...
590 Enterococcus faecalis mevalonate kinase
615 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
616 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
617 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
618 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
619 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
620 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
621 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
622 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
623 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
624 Rapid evolution of beta-glucuronidase specificity by saturation mutagenesis of an active site loop
625 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
626 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
627 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
628 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
629 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
630 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
631 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
632 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
633 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
634 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
635 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
636 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
637 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
638 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
639 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
640 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
641 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
642 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
643 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
644 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
645 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
646 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
647 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
648 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
649 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
650 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
651 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
652 Probing the dynamics of a mobile loop above the active site of L1, a metallo-beta-lactamase from ...
653 UDP-glucuronic Acid:Anthocyanin Glucuronosyltransferase from Red Daisy (Bellis perennis) Flowers
654 UDP-glucuronic Acid:Anthocyanin Glucuronosyltransferase from Red Daisy (Bellis perennis) Flowers
655 Mass spectrometric characterization of a three-enzyme tandem reaction for assembly and modification of the ...
656 Mass spectrometric characterization of a three-enzyme tandem reaction for assembly and modification of the ...
657 Mass spectrometric characterization of a three-enzyme tandem reaction for assembly and modification of the ...
658 Mass spectrometric characterization of a three-enzyme tandem reaction for assembly and modification of the ...
659 Mass spectrometric characterization of a three-enzyme tandem reaction for assembly and modification of the ...
660 A new kinetic model of recombinant beta-galactosidase from Kluyveromyces lactis for both hydrolysis and ...
661 A new kinetic model of recombinant beta-galactosidase from Kluyveromyces lactis for both hydrolysis and ...
662 A new kinetic model of recombinant beta-galactosidase from Kluyveromyces lactis for both hydrolysis and ...
663 The Effect of Adenylic Acid on Yeast Nicotinamide Adenine Dinucleotide Isocitrate Dehydrogenase, a Possible ...
664 Kinetic Mechanism of Histone Acetyltransferase GCN5 from Yeast
665 Kinetic Mechanism of Histone Acetyltransferase GCN5 from Yeast
666 Kinetic Mechanism of Histone Acetyltransferase GCN5 from Yeast
667 Kinetic Mechanism of Histone Acetyltransferase GCN5 from Yeast
668 Kinetic Mechanism of Histone Acetyltransferase GCN5 from Yeast
669 Kinetic Mechanism of Histone Acetyltransferase GCN5 from Yeast
670 Kinetic studies on the mechanism and regulation of rabbit liver fructose-1,6 -bisphosphatase
671 Kinetic studies on the mechanism and regulation of rabbit liver fructose-1,6 -bisphosphatase
672 Kinetic studies on the mechanism and regulation of rabbit liver fructose-1,6 -bisphosphatase
673 Kinetic studies on the mechanism and regulation of rabbit liver fructose-1,6 -bisphosphatase
674 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
675 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
676 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
677 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
678 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
679 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
680 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
681 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
682 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
683 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
684 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
685 Human brain 6-phosphogluconate dehydrogenase: purification and kinetic properties
686 Novel type of glucose-6-phosphate isomerase in the hyperthermophilic archaeon Pyrococcus furiosus
687 Novel type of glucose-6-phosphate isomerase in the hyperthermophilic archaeon Pyrococcus furiosus
688 Novel type of glucose-6-phosphate isomerase in the hyperthermophilic archaeon Pyrococcus furiosus
689 Novel type of glucose-6-phosphate isomerase in the hyperthermophilic archaeon Pyrococcus furiosus
690 Identifcation and functional characterization of leukotriene B4 20- hydroxylase of human polymorphonuclear ...
691 Identifcation and functional characterization of leukotriene B4 20- hydroxylase of human polymorphonuclear ...
696 Purification and characterization of avian dopamine beta-hydroxylase
697 Purification and characterization of avian dopamine beta-hydroxylase
698 Purification and characterization of avian dopamine beta-hydroxylase
699 Multiple forms of Human Red Blood Cell Hexokinase
700 Multiple forms of Human Red Blood Cell Hexokinase
701 Multiple forms of Human Red Blood Cell Hexokinase
702 Multiple forms of Human Red Blood Cell Hexokinase
703 Multiple forms of Human Red Blood Cell Hexokinase
704 Multiple forms of Human Red Blood Cell Hexokinase
705 Multiple forms of Human Red Blood Cell Hexokinase
706 Multiple forms of Human Red Blood Cell Hexokinase
707 Multiple forms of Human Red Blood Cell Hexokinase
708 Multiple forms of Human Red Blood Cell Hexokinase
709 Multiple forms of Human Red Blood Cell Hexokinase
710 Multiple forms of Human Red Blood Cell Hexokinase
711 Multiple forms of Human Red Blood Cell Hexokinase
712 Multiple forms of Human Red Blood Cell Hexokinase
713 Multiple forms of Human Red Blood Cell Hexokinase
714 Multiple forms of Human Red Blood Cell Hexokinase
715 Multiple forms of Human Red Blood Cell Hexokinase
716 Multiple forms of Human Red Blood Cell Hexokinase
717 Multiple forms of Human Red Blood Cell Hexokinase
718 Multiple forms of Human Red Blood Cell Hexokinase
719 Multiple forms of Human Red Blood Cell Hexokinase
720 NAD-dependent Methylenetetrahydrofolate Dehydrogenase-Methenyltetrahydrofolate Cyclohydrolase from Ascites ...
721 Probing the location and function of the conserved histidine residue of phosphoglucose isomerase by using an ...
722 Probing the location and function of the conserved histidine residue of phosphoglucose isomerase by using an ...
723 Probing the location and function of the conserved histidine residue of phosphoglucose isomerase by using an ...
724 Probing the location and function of the conserved histidine residue of phosphoglucose isomerase by using an ...
725 Probing the location and function of the conserved histidine residue of phosphoglucose isomerase by using an ...
726 Probing the location and function of the conserved histidine residue of phosphoglucose isomerase by using an ...
727 Evidence for the involvement of arginyl residue at the active site of penicillin G acylase from Kluyvera ...
728 Evidence for the involvement of arginyl residue at the active site of penicillin G acylase from Kluyvera ...
729 Evidence for the involvement of arginyl residue at the active site of penicillin G acylase from Kluyvera ...
730 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
731 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
732 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
733 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
734 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
735 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
736 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
737 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
738 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
739 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
740 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
741 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
742 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
743 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
744 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
745 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
746 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
747 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
748 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
749 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
750 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
751 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
752 Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the ...
753 Identification and mechanism of a bacterial hydrolyzing UDP-N-acetylglucosamine 2-epimerase.
760 Purification and Properties of Human Erythrocyte Membrane NADH- Cytochrome b5 Reductase
761 Purification and Properties of Human Erythrocyte Membrane NADH- Cytochrome b5 Reductase
762 Purification and Properties of Human Erythrocyte Membrane NADH- Cytochrome b5 Reductase
763 Purification and Properties of Human Erythrocyte Membrane NADH- Cytochrome b5 Reductase
782 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
783 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
784 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
785 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
786 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
787 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
788 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
789 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
790 Structure-based engineering of Alcaligenes xylosoxidans copper-containing nitrite reductase enhances ...
817 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
818 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
819 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
820 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
821 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
822 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
823 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
824 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
825 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
826 Structural insights into the Thermus thermophilus ADP-ribose pyrophosphatase mechanism via crystal structures ...
905 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
906 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
907 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
908 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
909 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
910 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
911 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
912 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
913 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
914 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
915 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
916 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
917 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
918 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
919 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
920 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
921 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
922 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
923 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
924 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
925 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
926 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
927 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
928 Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the ...
933 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
934 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
935 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
936 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
937 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
938 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
939 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
940 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
941 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
942 Active site mutants of the "non-hydrolyzing" UDP-N-acetylglucosamine 2-epimerase from Escherichia coli
943 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
944 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
945 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
946 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
947 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
948 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
949 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
950 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
951 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
952 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
953 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
954 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
955 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
956 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
957 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
958 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
959 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
960 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
961 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
962 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
963 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
964 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
965 Catalytic mechanism of alpha-retaining glucosyl transfer by Corynebacterium callunae starch phosphorylase: the ...
966 The carboligation reaction of acetohydroxyacid synthase II: steady-state intermediate distributions in wild ...
967 The carboligation reaction of acetohydroxyacid synthase II: steady-state intermediate distributions in wild ...
968 The carboligation reaction of acetohydroxyacid synthase II: steady-state intermediate distributions in wild ...
969 The carboligation reaction of acetohydroxyacid synthase II: steady-state intermediate distributions in wild ...
970 The carboligation reaction of acetohydroxyacid synthase II: steady-state intermediate distributions in wild ...
971 Inhibition of type I and type II phosphomannose isomerases by the reaction intermediate analogue ...
972 Inhibition of type I and type II phosphomannose isomerases by the reaction intermediate analogue ...
973 Inhibition of type I and type II phosphomannose isomerases by the reaction intermediate analogue ...
974 Inhibition of type I and type II phosphomannose isomerases by the reaction intermediate analogue ...
979 Identification, characterization, and site-directed mutagenesis of recombinant pentachlorophenol ...
980 Identification, characterization, and site-directed mutagenesis of recombinant pentachlorophenol ...
981 Identification, characterization, and site-directed mutagenesis of recombinant pentachlorophenol ...
982 Identification, characterization, and site-directed mutagenesis of recombinant pentachlorophenol ...
983 Identification, characterization, and site-directed mutagenesis of recombinant pentachlorophenol ...
984 Identification, characterization, and site-directed mutagenesis of recombinant pentachlorophenol ...
985 Nikkomycin biosynthesis: formation of a 4-electron oxidation product during turnover of NikD with its ...
986 Nikkomycin biosynthesis: formation of a 4-electron oxidation product during turnover of NikD with its ...
987 The Catalytic Mechanism of the Glutathione-Dependent Dehydroascorbate Reductase Activity of Thioltransferase ...
988 The Catalytic Mechanism of the Glutathione-Dependent Dehydroascorbate Reductase Activity of Thioltransferase ...
989 The Catalytic Mechanism of the Glutathione-Dependent Dehydroascorbate Reductase Activity of Thioltransferase ...
990 The Catalytic Mechanism of the Glutathione-Dependent Dehydroascorbate Reductase Activity of Thioltransferase ...
991 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
992 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
993 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
994 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
995 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
996 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
997 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
998 Biochemical diversity among the 1-amino-cyclopropane-1-carboxylate synthase isozymes encoded by the ...
999 Structural studies of the catalytic reaction pathway of a hyperthermophilic histidinol-phosphate ...
1000 Structural studies of the catalytic reaction pathway of a hyperthermophilic histidinol-phosphate ...



Overview of the Entry Data   (go to Help / Information Video Turorials )
 One line in Overview represents one entry in the database.
 Click on the key/axis name to sort by that key. Hover over the heatmap to see the data values.
 Select values by clicking on the heatmap area. Multiple categories or ranges are selected by brushing.
 Overview visible axis/keys can be set in 'Visible Overview Axes' (click to open/close)
 Selection on all graphs can be reset by using 'Reset Highlighting'.
 Selected color scheme (set in 'Color Scheme (PC, SPM, KPPC, KPSP)'): Plasma (Warm, Dark)
  

    * Keys/axis take the appropriate selection from the whole color scheme (color legend can be seen when sorting by that key) e.g.
    two valued keys (e.g. Rate Equation) use the end colors of the color scheme while unique numerical keys (e.g. EntryID) use the whole color scheme.
    * Overview shows the coloring by every key/axis (best seen when sorted by that axis/key).
    All other graphs (PC, SPM, KPPC, KPSP) use one single axis/key for coloring (chosen in 'PC, SPM: color by axis', 'KPPC, KPSP: color by axis').
    * Non-existent values of a chosen key can be made more prominent by separately selecting their color in 'NULL ("-") value color (for all graphs)':     Default (color scale minimum) selected
Highlighted Data:

0






Axes:


Allowing only eight (seven plus Index) visible PC axis to prevent clutter.

SPM full matrix


Height of the PC and KPPC graphs is limited to 1200px. If the graph is larger some tick clutter might appear on the axes.


Kinetic Parameter Data:



Appearance:

Color Scheme
(PC, SPM, KPPC, KPSP)


NULL ("-") value color
(for all graphs)
The "null" color is visible if the data is sorted by the key that contains the null values.

PC, SPM: color by axis

KPPC, KPSP: color by axis


Various:


Parallel Coordinates (PC) of the Entry Data
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 Brush the axis to select the data (supports multiple selections).
 Detailed numerical data values can be seen on Overview or SPM (or in the Entry View tab).
 PC visible axis/keys can be set in 'Visible PC Axes (max 8)'
 PC colored by the key (set in 'PC, SPM: color by axis'):
Scatter Plot Matrix (SPM) of the Entry Data (numerical values only -> pH, Temperature, Year; kinetic data separately)
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 Brush any of the scatter plots to select the data.
 SPM visible axis/keys can be set in 'Visible SPM Axes'
 SPM colored by the key (set in 'PC, SPM: color by axis'):
Kinetic Parameters
Parallel Coordinates (KPPC) of the Kinetic Parameters (plus temperature, pH) (each entry can have many parameters)
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 Each entry can have multiple kinetic parameters that can be explored in the two graphs (KPPC, KPSP).
 Brush the axis to select the data.
 Detailed numerical data values can be seen on scatter plot KPSP (or in the Entry View tab).
 KPPC visible axis/keys can be set in 'Visible KPPC Axes'
 Currently showing types (set in 'Used Data Types'):
 KPPC colored by the key (set in 'KPPC, KPSP: color by axis'):
 KPPC, KPSP using the color scheme (set in 'Color Scheme (PC, SPM, KPPC, KPSP)'):
 Use KPSP to see the parameter details.
 KPPC local zoom status (allows detailed parameter space exploration not possible through the search):
    Parameter data types have to be reselected on zoom out (set in 'Used Data Types'). Not all types are available when zoomed.


Search button will give you the entries with all of thier parameters.
Limit the search locally first, by zooming and then selecting for the search.
Not selecting anything before the search will give you the initial result.





Scatter Plot (KPSP) of the Kinetic Parameter Values (plus temperature, pH) (each entry can have many parameters)
Loading graph, please wait...


  Points currently colored by:
 KPSP currently showing: Start Value vs
 KPSP serves as a addition of KPPC to see the parameter details (hover over point to see the values).
 Data can be zoomed and panned, but should be selected on KPPC.
Show/hide Video Turorials
First three graphs represent the general information for the database entries (Overview, PC, SPM).
Since each entry can contain several kinetic parameters, data space of the kinetic parameters can be separately explored (using KPPC and KPSP).
Last two graphs offer more details about the kinetic parameters (KPPC, KPSP) belonging to the entries and an option to explore through their data space.
A number of entries is obtained as a result of a search.

Select/highlight the subset of the data on one of the graphs. Number of highlighted data and the used attributes are visible on the top right side of the visualization tab (as is the number of the selected kinetic parameters).
By clicking on "Add Selection to Search" search is performed applying the selected criteria (highlighting) on the resulting data, thus refining the search. E.g.
If the current search query is a refinement of the previous query "Use Previous Query (Go Back)" button can be used to perform the previous query again. Only one automatic step back is possible, but the query can be manually manipulated if desired.


The graphs can be manipulated and the data highlighted in the following ways:

Overview of the resulting data entries is given in the heat map:
* Sort per column (upwards, downwards) by clicking on the attribute's title, hold the "shift" key and drag the column to rearrange columns.
* Show/hide columns using Visible Overview Axes.
* Highlight individual values by clicking.
* Highlight ranges by brushing (range of the sorted column, marked with a green line).
* While brushing, the thin green line (extending from the thick one) shows the full range of the selected categories.

Parallel Coordinates (PC):
* Sort axis by double clicking on the axis title, rearrange axes by dragging.
* Show/hide axes using Visible PC Axes (maximum 7 in addition to the Index axis).
* Highlight ranges by brushing on different axes (more ranges on a single axis are possible).
* Height of the PC graph is determined by the data, but limited (has minimum and maximum height). If the graph should be larger than the maximum height some tick clutter might appear on the axes.
* Numerical axes (e.g. pH and Temperature) have their null values shown below the line unlike categorical axes (like UniprotID) that have the null value or "-" as a category on the axis.

Scatter Plot Matrix (SPM):
* Show/hide attributes (numerical ones) using Visible SPM Axes.
* Highlight range by brushing on one of the scatter plots.
* Histograms show the attribute value frequency (divided into 10 bins/columns).
* Full SPM matrix can be shown.
* Details about the point values can be seen on a tooltip when hovering above the point.
* Points with no value ("-") are shown on the left side or under the axis.
* If only points with no value ("-") are present, they are shown under or left of the zero line on the bottom/left of the respective image.
* Lower tick values are valid for the histogram graphs while ticks on the left (plus the lower ones) are only valid for the scatter plots in the matrix.

Kinetic Parameter Parallel Coordinates (KPPC):
* EntryID axis on KPPC connects the kinetic parameters with the other graphs: each parameter belongs to an entry. One entry can have more parameters.
* Sort axis by double clicking on the axis title, rearrange axes by dragging.
* Show/hide axes using Visible KPPC Axes (Type and EntryID are always visible).
* Highlight ranges by brushing on different axes (single range possible on a single axis).
* Select shown kinetic parameter data type by selecting Used Data Types (must be at least one).
     * Types are preselected on search giving types: Km, Vmax, kcat as default (if present). The user can view any other type by selecting it in the GUI.
     * Currently selected types are stated below the graph.
* Start Value Original axis shows the original values of the parameter.
* Start Value Log axis is a logarithmic axis (since the original range of the shown values can be huge). The original range can be seen in Brush Info Kinetic Parameters PC.
* Graph can be searched locally by using the Zoom in / Zoom out buttons.
* Once the desired values are narrowed down (and selected on the KPPC) they can be searched by using the "Add Selection to Search" button.
     * the kinetic parameter search query uses the selected keywords (where available) e.g. ParameterType, AssociatedSpecies.
     * where no keywords are available the kinetic parameter search query uses entryIDs.
     * the result of the search gives full entries (meaning resulting parameter data is bigger than the selection).
* Height of the KPPC graph is determined by the data, but limited (has minimum and maximum height). If the graph should be larger than the maximum height some tick clutter might appear on the axes.
* For convenience, KPPC can also show temperature and pH values and the axis can also be colored by those values.
* Numerical axes (e.g. pH and Temperature) have their null values shown below the line unlike categorical axes that have the null value or "-" as a category on the axis.

Scatter Plot of the Kinetic Parameter Values (KPSP):
* Scatter plot is showing the values of the "Start Value Original" vs "Temperature", "pH" or "EntryID" values.
* The user can choose values on the y axis using the dropdown menu ("Temperature", "pH" or "EntryID") above the graph.
* The user can choose the axis used for the point size using the dropdown menu ("Uniform", "Temperature", "pH" or "EntryID") above the graph. Point size is interpolated between a set range (size 5 to 10). Larger range [1,30] can be set by using the range slider. Uniform size is size 5 (no range slider).
* The user can choose the kinetic parameter types of the shown values in the GUI using "Used data types" (the graph updates accordingly).
* Graph can be zoomed and panned by using the computer mouse or touchpad.
* Viewed data points can again be centered by pressing the Reset position button (zoom value is seen above the button).
* Details about the point values can be seen in a tooltip when hovering above the point.
* Points with no value ("-") are shown under the axis.
* If only points with no value ("-") are present, they are shown under the zero line.
* Used data types, their units and associated species are visible on the Start Value axis label (all can be seen in a tooltip when hovering above with the mouse pointer).
* Corresponding data is highlighted when selecting data on any of the other graphs.
* Data cannot be selected on this graph. The graph responds to the selection on the KPPC.
* Details about selection (made on KPPC) can be viewed below in the Brush Info section.

Additional Information:
* Highlighting data entries on one of the graphs (Overview, PC, SPM) highlights the same data on all other graphs (and their parameters on KPPC, KPSP).
* Highlighting kinetic parameter data on KPPC graph highlights the matching entries on other graphs (Overview, PC, SPM, KPSP). Each parameter belongs to an entry. One entry can have more parameters.
* Details about selection can be viewed below in the Brush Info section.
* Reset highlighted values by using "Reset Highlighting".
* Index attribute is only the sequential numbering of the result and cannot be used for further searching.
* Color:
     * Different color schemes for the graphs can be selected (see image).
     * Overview uses the full range of the color scheme for each of the attributes.
     * Which attribute is used for coloring PC and SPM axes can be manually selected, otherwise it changes upon sorting columns in Overview.
     * Which attribute is used for coloring KPPC axes (and KPSP) can also be manually selected (and does not change upon sorting columns in Overview).
     * Color of the null values can be selected by using the "NULL ("-") value color" in the GUI. Default color is the faded minimum color of the chosen color scheme. Users can select another color that offers more contrast and visibility in combination with the chosen color scheme (red, green, blue, cyan, magenta, yellow, black). When changing the used color scheme the null color is reset to the default color for that scheme (faded minimum color). Note that coloring ("PC, SPM: color by axis") or sorting the Overview (and hence coloring PC and SPM) by a certain key/axis (containing the null values), makes the null values nicely visible on the PC and SPM graphs. For the null value color to be visible on the KPPC and KPSP graphs, they need to be colored by that key/axis ("KPPC, KPSP: color by axis").
* Screenshots of the produced graphs can be downloaded together with the solr search expression.
* Hovering with a pointer over a shortened tick name (three dots) shows the full name.
* Temperature is given in degrees Celsius (°C).
* Overview currently shows maximum 10000 data, PC and SPM maximum 400 (to not over clutter). The data limit for PC and SPM can be turned off by ticking "Allow More Data" in the GUI. This option only appears if the number of data entries is between 400 and 10000.
Brush Info