Structure of PDB 6cwj Chain B Binding Site BS02
Receptor Information
>6cwj Chain B (length=363) Species:
264732
(Moorella thermoacetica ATCC 39073) [
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HMQKVEVFRIPTASPDDISGLATLIDSGKINPAEIVAILGKTEGNGCVND
FTRGFATQSLAMYLAEKLGISREEVVKKVAFIMSGGTEGVMTPHITVFVR
KDVAAPAAPGKRLAVGVAFTRDFLPEELGRMEQVNEVARAVKEAMKDAQI
DDPRDVHFVQIKCPLLTAERIEDAKRRGKDVVVNDTYKSMAYSRGASALG
VALALGEISADKISNEAICHDWNLYSSVASTSAGVELLNDEIIVVGNSTN
SASDLVIGHSVMKDAIDADAVRAALKDAGIRSDDEMDRIVNVLAKAEAAS
SGTVRGRRNTMLDDSDINHTRSARAVVNAVIASVVGDPMVYVSGGAEHQG
PDGGGPIAVIARV
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
6cwj Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6cwj
Crystal structures of Moorella thermoacetica cyanuric acid hydrolase reveal conformational flexibility and asymmetry important for catalysis.
Resolution
2.253 Å
Binding residue
(original residue number in PDB)
E296 A345 Q348 G349 P350 G353
Binding residue
(residue number reindexed from 1)
E297 A346 Q349 G350 P351 G354
Annotation score
1
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
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:6cwj
,
PDBe:6cwj
,
PDBj:6cwj
PDBsum
6cwj
PubMed
31181074
UniProt
Q2RGM7
|CAH_MOOTA Cyanuric acid amidohydrolase (Gene Name=Moth_2120)
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