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4NQ5

Bacillus cereus Zn-dependent metallo-beta-lactamase at pH 7 complexed with compound CS319

Functional Information from GO Data
ChainGOidnamespacecontents
A0008270molecular_functionzinc ion binding
A0008800molecular_functionbeta-lactamase activity
A0016787molecular_functionhydrolase activity
A0017001biological_processantibiotic catabolic process
A0042597cellular_componentperiplasmic space
A0046677biological_processresponse to antibiotic
A0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 301
ChainResidue
AHIS86
AHIS88
AHIS149
A3C7303

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 302
ChainResidue
AASP90
ACYS168
AHIS210
A3C7303

site_idAC3
Number of Residues10
DetailsBINDING SITE FOR RESIDUE 3C7 A 303
ChainResidue
AHIS88
AASP90
AHIS149
ALYS171
AGLY179
AASN180
AHIS210
AZN301
AZN302
ATRP59

Functional Information from PROSITE/UniProt
site_idPS00743
Number of Residues20
DetailsBETA_LACTAMASE_B_1 Beta-lactamases class B signature 1. IiTHaHADriGGiktlker.G
ChainResidueDetails
AILE83-GLY102

site_idPS00744
Number of Residues13
DetailsBETA_LACTAMASE_B_2 Beta-lactamases class B signature 2. PqynILvGgCLVK
ChainResidueDetails
APRO159-LYS171

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues3
DetailsBINDING: BINDING => ECO:0000269|PubMed:20677753, ECO:0000269|PubMed:24059435, ECO:0000269|PubMed:26482303, ECO:0000269|PubMed:7588620, ECO:0000269|PubMed:9761898
ChainResidueDetails
AHIS86
AHIS88
AHIS149

site_idSWS_FT_FI2
Number of Residues3
DetailsBINDING: BINDING => ECO:0000269|PubMed:20677753, ECO:0000269|PubMed:24059435, ECO:0000269|PubMed:26482303
ChainResidueDetails
AASP90
ACYS168
AHIS210

site_idSWS_FT_FI3
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:26482303
ChainResidueDetails
ALYS171

site_idSWS_FT_FI4
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:26482303, ECO:0000269|PubMed:9761898
ChainResidueDetails
AASN180

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 16
ChainResidueDetails
AHIS86metal ligand
AHIS88metal ligand
AASP90hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AHIS149metal ligand
AASN180electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2024-07-24

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