4KU3
Crystal Structure of C143S Xanthomonas Campestris OleA bound with myristic acid and myrisotoyl-CoA
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0005737 | cellular_component | cytoplasm |
A | 0016740 | molecular_function | transferase activity |
A | 0016746 | molecular_function | acyltransferase activity |
A | 0044550 | biological_process | secondary metabolite biosynthetic process |
A | 0046872 | molecular_function | metal ion binding |
B | 0005737 | cellular_component | cytoplasm |
B | 0016740 | molecular_function | transferase activity |
B | 0016746 | molecular_function | acyltransferase activity |
B | 0044550 | biological_process | secondary metabolite biosynthetic process |
B | 0046872 | molecular_function | metal ion binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE PEG A 401 |
Chain | Residue |
A | LEU198 |
A | HOH676 |
A | HOH738 |
A | ALA199 |
A | THR248 |
A | THR250 |
A | VAL287 |
A | SER288 |
A | HIS291 |
A | HOH616 |
A | HOH633 |
site_id | AC2 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE PEG A 402 |
Chain | Residue |
A | ASP35 |
A | ARG73 |
A | ILE309 |
A | GLU312 |
A | HIS313 |
A | HOH658 |
A | HOH705 |
A | HOH717 |
site_id | AC3 |
Number of Residues | 13 |
Details | BINDING SITE FOR RESIDUE MYR B 401 |
Chain | Residue |
B | SER143 |
B | LEU253 |
B | GLY257 |
B | ILE258 |
B | ILE284 |
B | HIS285 |
B | HIS291 |
B | ASN315 |
B | LEU343 |
B | ILE345 |
B | GLY346 |
B | SER347 |
B | MYA402 |
site_id | AC4 |
Number of Residues | 24 |
Details | BINDING SITE FOR RESIDUE MYA B 402 |
Chain | Residue |
B | THR60 |
B | VAL66 |
B | ALA67 |
B | SER112 |
B | GLU171 |
B | THR172 |
B | PHE194 |
B | ARG195 |
B | LEU198 |
B | ALA199 |
B | THR202 |
B | CYS239 |
B | ASN242 |
B | THR250 |
B | ARG251 |
B | LEU253 |
B | VAL287 |
B | SER288 |
B | PRO290 |
B | GLY317 |
B | MYR401 |
B | HOH511 |
B | HOH524 |
B | HOH662 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"PubMed","id":"22524624","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"27815501","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"29025976","evidenceCode":"ECO:0000305"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | Active site: {"description":"Acyl-thioester intermediate","evidences":[{"source":"PubMed","id":"22524624","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"27815501","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"29025976","evidenceCode":"ECO:0000305"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 4 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"22524624","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"29025976","evidenceCode":"ECO:0000269"},{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"SEP-2017","submissionDatabase":"PDB data bank","title":"The role of OleA His285 in substrate coordination of long-chain acyl-CoA.","authors":["Jensen M.R.","Goblirsch B.R.","Esler M.A.","Christenson J.K.","Mohamed F.A.","Wackett L.P.","Wilmot C.M."]}}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | Site: {"description":"Important for activity","evidences":[{"source":"PubMed","id":"29430657","evidenceCode":"ECO:0000305"}]} |
Chain | Residue | Details |