2Q7Q
Crystal structure of Alcaligenes faecalis AADH in complex with p-chlorobenzylamine.
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0030058 | molecular_function | aliphatic amine dehydrogenase activity |
A | 0030059 | molecular_function | aralkylamine dehydrogenase (azurin) activity |
A | 0042597 | cellular_component | periplasmic space |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0030058 | molecular_function | aliphatic amine dehydrogenase activity |
B | 0030059 | molecular_function | aralkylamine dehydrogenase (azurin) activity |
B | 0042597 | cellular_component | periplasmic space |
D | 0009308 | biological_process | amine metabolic process |
D | 0016491 | molecular_function | oxidoreductase activity |
D | 0016638 | molecular_function | oxidoreductase activity, acting on the CH-NH2 group of donors |
D | 0030059 | molecular_function | aralkylamine dehydrogenase (azurin) activity |
D | 0042597 | cellular_component | periplasmic space |
H | 0009308 | biological_process | amine metabolic process |
H | 0016491 | molecular_function | oxidoreductase activity |
H | 0016638 | molecular_function | oxidoreductase activity, acting on the CH-NH2 group of donors |
H | 0030059 | molecular_function | aralkylamine dehydrogenase (azurin) activity |
H | 0042597 | cellular_component | periplasmic space |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE C2B H 2001 |
Chain | Residue |
A | PHE97 |
H | HOH2018 |
A | ASN124 |
A | GLN177 |
A | GLY178 |
H | ASP84 |
H | TRQ109 |
H | ASN156 |
H | VAL158 |
H | ASN159 |
site_id | AC2 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE C2B D 2002 |
Chain | Residue |
B | ASN124 |
B | GLN177 |
B | GLY178 |
D | ASP84 |
D | TRQ109 |
D | ASN156 |
D | VAL158 |
D | ASN159 |
D | HOH2067 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | Active site: {"description":"Tryptophylquinone 6'-substrate hemiaminal intermediate"} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"PubMed","id":"16614214","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17005560","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 6 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"16614214","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17005560","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | Site: {"description":"Transition state stabilizer"} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 2 |
Details | Modified residue: {"description":"Tryptophylquinone","evidences":[{"source":"PubMed","id":"16614214","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17005560","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17087503","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI6 |
Number of Residues | 6 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"16614214","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17005560","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17087503","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 2bbk |
Chain | Residue | Details |
D | THR172 | |
D | ASP84 | |
D | PHE169 | |
D | TRP160 | |
D | ASP128 |
site_id | CSA2 |
Number of Residues | 5 |
Details | Annotated By Reference To The Literature 2bbk |
Chain | Residue | Details |
H | THR172 | |
H | ASP84 | |
H | PHE169 | |
H | TRP160 | |
H | ASP128 |