Structure of PDB 6buo Chain B Binding Site BS07
Receptor Information
>6buo 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
PDO
InChI
InChI=1S/C3H8O2/c4-2-1-3-5/h4-5H,1-3H2
InChIKey
YPFDHNVEDLHUCE-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(CO)CO
ACDLabs 11.02
CACTVS 3.352
OCCCO
Formula
C3 H8 O2
Name
1,3-PROPANDIOL
ChEMBL
CHEMBL379652
DrugBank
DB02774
ZINC
ZINC000001529437
PDB chain
6buo Chain B Residue 409 [
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Receptor-Ligand Complex Structure
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PDB
6buo
Crystal structures of Moorella thermoacetica cyanuric acid hydrolase reveal conformational flexibility and asymmetry important for catalysis.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
K187 A190 H323 E351
Binding residue
(residue number reindexed from 1)
K188 A191 H319 E347
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
View graph for
Biological Process
External links
PDB
RCSB:6buo
,
PDBe:6buo
,
PDBj:6buo
PDBsum
6buo
PubMed
31181074
UniProt
Q2RGM7
|CAH_MOOTA Cyanuric acid amidohydrolase (Gene Name=Moth_2120)
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