Structure of PDB 6bup Chain A Binding Site BS03
Receptor Information
>6bup Chain A (length=361) Species:
264732
(Moorella thermoacetica ATCC 39073) [
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HMQKVEVFRIPTASPDDISGLATLIDSGKINPAEIVAILGKTEGNGCVND
FTRGFATQSLAMYLAEKLGISREEVVKKVAFIMSGGTEGVMTPHITVFVR
KDVAAPPGKRLAVGVAFTRDFLPEELGRMEQVNEVARAVKEAMKDAQIDD
PRDVHFVQIKCPLLTAERIEDAKRRGKDVVVNDTYKSMAYSRGASALGVA
LALGEISADKISNEAICHDWNLYSSVASTSAGVELLNDEIIVVGNSTNSA
SDLVIGHSVMKDAIDADAVRAALKDAGIRSDDEMDRIVNVLAKAEAASSG
TVRGRRNTMLDDSDINHTRSARAVVNAVIASVVGDPMVYVSGGAEHQGPD
GGGPIAVIARV
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
6bup Chain A Residue 405 [
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Receptor-Ligand Complex Structure
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PDB
6bup
Crystal structures of Moorella thermoacetica cyanuric acid hydrolase reveal conformational flexibility and asymmetry important for catalysis.
Resolution
1.88 Å
Binding residue
(original residue number in PDB)
K187 C218 W221
Binding residue
(residue number reindexed from 1)
K186 C217 W220
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:6bup
,
PDBe:6bup
,
PDBj:6bup
PDBsum
6bup
PubMed
31181074
UniProt
Q2RGM7
|CAH_MOOTA Cyanuric acid amidohydrolase (Gene Name=Moth_2120)
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