1DAE
DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 3-(1-AMINOETHYL) NONANEDIOIC ACID
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000166 | molecular_function | nucleotide binding |
A | 0000287 | molecular_function | magnesium ion binding |
A | 0004141 | molecular_function | dethiobiotin synthase activity |
A | 0005524 | molecular_function | ATP binding |
A | 0005737 | cellular_component | cytoplasm |
A | 0005829 | cellular_component | cytosol |
A | 0009102 | biological_process | biotin biosynthetic process |
A | 0016874 | molecular_function | ligase activity |
A | 0042803 | molecular_function | protein homodimerization activity |
A | 0046872 | molecular_function | metal ion binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 12 |
Details | BINDING SITE FOR RESIDUE IKT A 225 |
Chain | Residue |
A | LYS37 |
A | HOH342 |
A | HOH343 |
A | HOH360 |
A | ALA40 |
A | SER41 |
A | PRO79 |
A | GLY150 |
A | CYS151 |
A | ILE152 |
A | ASN153 |
A | TYR187 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 1 |
Details | Active site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00336","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"9125495","evidenceCode":"ECO:0000305"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 8 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00336","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"7669756","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9576910","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9865950","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1A82","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1BS1","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAD","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAF","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAG","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAH","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAK","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAM","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 1 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"9865950","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1BS1","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 3 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00336","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"9576910","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9865950","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1A82","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1BS1","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAK","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAM","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 1 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00336","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"7669756","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9576910","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9865950","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1BS1","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAE","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAF","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAG","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAH","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAI","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAK","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAM","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI6 |
Number of Residues | 3 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00336","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"9576910","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1A82","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAK","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI7 |
Number of Residues | 1 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"7669756","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9576910","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9865950","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1A82","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1BS1","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAE","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAF","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAG","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAH","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAI","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAK","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DAM","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | -1 |
Details | a catalytic site defined by CSA, PubMed 19301336 |
Chain | Residue | Details |
site_id | MCSA1 |
Number of Residues | 8 |
Details | M-CSA 74 |
Chain | Residue | Details |
A | THR11 | electrostatic stabiliser |
A | GLU12 | metal ligand |
A | LYS15 | electrostatic stabiliser, hydrogen bond donor |
A | THR16 | metal ligand |
A | LYS37 | electrostatic stabiliser, hydrogen bond donor |
A | SER41 | electrostatic stabiliser, hydrogen bond donor |
A | ASP54 | metal ligand |
A | GLU115 | metal ligand |