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4CS0

Direct visualisation of strain-induced protein post-translational modification

Functional Information from GO Data
ChainGOidnamespacecontents
A0004068molecular_functionaspartate 1-decarboxylase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006523biological_processalanine biosynthetic process
A0015940biological_processpantothenate biosynthetic process
A0016540biological_processprotein autoprocessing
A0016829molecular_functionlyase activity
A0016831molecular_functioncarboxy-lyase activity
B0005515molecular_functionprotein binding
B0015940biological_processpantothenate biosynthetic process
B0016485biological_processprotein processing
B0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
B0031638biological_processzymogen activation
B1905502molecular_functionacetyl-CoA binding
Functional Information from PDB Data
site_idAC1
Number of Residues23
DetailsBINDING SITE FOR RESIDUE ACO B 1128
ChainResidue
AARG102
BARG74
BARG75
BGLY76
BVAL77
BGLY78
BGLN79
BVAL102
BGLU103
BVAL107
BMET108
BTRP23
BPHE111
BMG1129
BHOH2016
BHOH2021
BGLU25
BTYR26
BSER65
BLEU66
BARG67
BVAL68
BARG73

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG B 1129
ChainResidue
BTHR72
BARG73
BARG74
BARG75
BGLY76
BVAL77
BACO1128

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SCN A 1127
ChainResidue
AALA25
ATRP47
AARG54
ATHR57
AALA74
AALA75
AILE86

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsActive site: {"description":"Schiff-base intermediate with substrate; via pyruvic acid","evidences":[{"source":"PubMed","id":"9546220","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues1
DetailsActive site: {"description":"Proton donor"}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues3
DetailsBinding site: {"evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues1
DetailsModified residue: {"description":"Pyruvic acid (Ser)","evidences":[{"source":"PubMed","id":"9546220","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues126
DetailsDomain: {"description":"N-acetyltransferase","evidences":[{"source":"HAMAP-Rule","id":"MF_02018","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues15
DetailsRegion: {"description":"Interaction with PanD","evidences":[{"source":"PubMed","id":"25910242","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues9
DetailsBinding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_02018","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"25910242","evidenceCode":"ECO:0000269"},{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"JUN-2008","submissionDatabase":"PDB data bank","title":"Solution NMR structure of putative N-acetyl transferase YhhK from E. coli bound to coenzyme A.","authors":["Cort J.R.","Yee A.","Arrowsmith C.H.","Kennedy M.A."]}},{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"MAR-2014","submissionDatabase":"PDB data bank","title":"Direct visualisation of strain-induced protein post-translational modification.","authors":["Monteiro D.C.F.","Patel V.","Bartlett C.P.","Grant T.D.","Nozaki S.","Gowdy J.A.","Snell E.H.","Niki H.","Pearson A.R.","Webb M.E."]}},{"source":"PDB","id":"2K5T","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idMCSA1
Number of Residues3
DetailsM-CSA 409
ChainResidueDetails
ALYS9electrostatic stabiliser
AALA25covalently attached, electrofuge, electrophile
ATYR58activator, increase nucleophilicity, proton acceptor, proton donor

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PDB entries from 2025-10-29

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