Structure of PDB 4bvq Chain B Binding Site BS02

Receptor Information
>4bvq Chain B (length=364) Species: 47660 (Pseudomonas sp. ADP) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
HMYHIDVFRIPCHSPGDTSGLEDLIETGRVAPADIVAVMGKTEGNGCVND
YTREYATAMLAACLGRHLQLPPHEVEKRVAFVMSGGTEGVLSPHHTVFAR
RPAIDAHRPAGKRLTLGIAFTRDFLPEEIGRHAQITETAGAVKRAMRDAG
IASIDDLHFVQVKCPLLTPAKIASARSRGCAPVTTDTYESMGYSRGASAL
GIALATEEVPSSMLVDESVLNDWSLSSSLASASAGIELEHNVVIAIGMSE
QATSELVIAHGVMSDAIDAASVRRTIESLGIRSDDEMDRIVNVFAKAEAS
PDGVVRGMRHTMLSDSDINSTRHARAVTGAAIASVVGHGMVYVSGGAEHQ
GPAGGGPFAVIARA
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain4bvq Chain B Residue 1365 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB4bvq Cyanuric Acid Hydrolase: Evolutionary Innovation by Structural Concatenation.
Resolution1.9 Å
Binding residue
(original residue number in PDB)
E297 A346 Q349 P351 G354
Binding residue
(residue number reindexed from 1)
E298 A347 Q350 P352 G355
Annotation score1
Enzymatic activity
Enzyme Commision number 3.5.2.15: cyanuric acid amidohydrolase.
Gene Ontology
Molecular Function
GO:0016787 hydrolase activity
GO:0016812 hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides
GO:0018753 cyanuric acid amidohydrolase activity
GO:0046872 metal ion binding
Biological Process
GO:0019381 atrazine catabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:4bvq, PDBe:4bvq, PDBj:4bvq
PDBsum4bvq
PubMed23651355
UniProtP58329|CAH_PSESD Cyanuric acid amidohydrolase (Gene Name=atzD)

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