1WZI
Structural basis for alteration of cofactor specificity of Malate dehydrogenase from Thermus flavus
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0003824 | molecular_function | catalytic activity |
A | 0006099 | biological_process | tricarboxylic acid cycle |
A | 0006108 | biological_process | malate metabolic process |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0016615 | molecular_function | malate dehydrogenase activity |
A | 0016616 | molecular_function | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor |
A | 0019752 | biological_process | carboxylic acid metabolic process |
A | 0030060 | molecular_function | L-malate dehydrogenase (NAD+) activity |
B | 0003824 | molecular_function | catalytic activity |
B | 0006099 | biological_process | tricarboxylic acid cycle |
B | 0006108 | biological_process | malate metabolic process |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0016615 | molecular_function | malate dehydrogenase activity |
B | 0016616 | molecular_function | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor |
B | 0019752 | biological_process | carboxylic acid metabolic process |
B | 0030060 | molecular_function | L-malate dehydrogenase (NAD+) activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 21 |
Details | BINDING SITE FOR RESIDUE NDP A 1334 |
Chain | Residue |
A | GLY13 |
A | GLY129 |
A | ASN130 |
A | MET154 |
A | LEU157 |
A | HIS186 |
A | SER240 |
A | HOH1336 |
A | HOH1343 |
A | HOH1412 |
A | HOH1434 |
A | GLN14 |
A | HOH1442 |
A | HOH1467 |
A | ILE15 |
A | GLY41 |
A | SER42 |
A | SER45 |
A | GLY87 |
A | ALA88 |
A | VAL128 |
site_id | AC2 |
Number of Residues | 20 |
Details | BINDING SITE FOR RESIDUE NDP B 2334 |
Chain | Residue |
B | GLY10 |
B | ALA11 |
B | ALA12 |
B | GLY13 |
B | GLN14 |
B | ILE15 |
B | LEU40 |
B | GLY41 |
B | SER42 |
B | SER45 |
B | ALA88 |
B | VAL128 |
B | GLY129 |
B | ASN130 |
B | MET154 |
B | HIS186 |
B | SER240 |
B | HOH2348 |
B | HOH2358 |
B | HOH2630 |
Functional Information from PROSITE/UniProt
site_id | PS00068 |
Number of Residues | 13 |
Details | MDH Malate dehydrogenase active site signature. MTRLDhnRAkaqL |
Chain | Residue | Details |
A | MET154-LEU166 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"HAMAP-Rule","id":"MF_01517","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 16 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01517","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"16009341","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"8471603","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 10 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01517","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01517","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"16009341","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1emd |
Chain | Residue | Details |
A | ASN185 | |
A | ASP158 |
site_id | CSA2 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1emd |
Chain | Residue | Details |
B | ASN185 | |
B | ASP158 |
site_id | CSA3 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1emd |
Chain | Residue | Details |
A | HIS186 | |
A | ARG161 | |
A | ASP158 |
site_id | CSA4 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1emd |
Chain | Residue | Details |
B | HIS186 | |
B | ARG161 | |
B | ASP158 |