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3CG5

Crystal Structure of the Covalent Adduct Formed between TB B-lactamase and Clavulanate

Functional Information from GO Data
ChainGOidnamespacecontents
A0005576cellular_componentextracellular region
A0005886cellular_componentplasma membrane
A0008800molecular_functionbeta-lactamase activity
A0016787molecular_functionhydrolase activity
A0017001biological_processantibiotic catabolic process
A0030655biological_processbeta-lactam antibiotic catabolic process
A0042597cellular_componentperiplasmic space
A0046677biological_processresponse to antibiotic
Functional Information from PDB Data
site_idAC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PO4 A 308
ChainResidue
AARG79
AARG187
AGLU193
AASP255
ATYR286
AHOH322
AHOH350
AHOH370

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE PO4 A 309
ChainResidue
ASER142
ATHR232
ATHR251
AGLY252
ATHR253
AHOH492
AHOH500
AHOH516
ASER84

site_idAC3
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PO4 A 310
ChainResidue
AARG75
AGLU78
AGLU184
AHOH324
AHOH346
AHOH410
AHOH536
AHOH545

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 A 311
ChainResidue
AASP218
ALYS219
ALYS235
AHOH465
AHOH474

site_idAC5
Number of Residues11
DetailsBINDING SITE FOR RESIDUE ISS A 684
ChainResidue
ACYS83
ASER84
ASER142
AGLU182
AASN186
AGLY252
ATHR253
AGLY254
AASP255
AHOH441
AHOH516

Functional Information from PROSITE/UniProt
site_idPS00146
Number of Residues16
DetailsBETA_LACTAMASE_A Beta-lactamase class-A active site. FaFCSTfKaplVAAVL
ChainResidueDetails
APHE80-LEU95

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsActive site: {"description":"Acyl-ester intermediate","evidences":[{"source":"PubMed","id":"19251630","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues1
DetailsActive site: {"description":"Proton acceptor","evidences":[{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000303"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000303"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues3
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"19251630","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues1
DetailsSite: {"description":"Increases nucleophilicity of active site Ser","evidences":[{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000303"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000303"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues1
DetailsSite: {"description":"Functions as a gatekeeper residue that regulates substrate accessibility to the enzyme active site","evidences":[{"source":"PubMed","id":"24023821","evidenceCode":"ECO:0000303"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1btl
ChainResidueDetails
ASER142
ASER84
AGLU182
ALYS87

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PDB entries from 2025-12-24

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