Structure of PDB 4nq3 Chain A Binding Site BS02
Receptor Information
>4nq3 Chain A (length=351) Species:
438753
(Azorhizobium caulinodans ORS 571) [
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MPIAKVHRIATASPDDVSGLAAAIATGAIAPAGILAIFGKTEGNGCVNDF
SRGFAVQSLQMLLRGHMGAAADEVCLVMSGGTEGGMSPHFLVFERAEGNA
PALAIGRAHTPDLPFEALGRMGQVRMVAQAVRRAMAAAGITDPEDVHFVQ
VKCPLLTAMRVKEAEARGATTATSDTLKSMGLSRGASALGIALALGEVAE
DALSDAVICADYGLWSARASCSSGIELLGHEIVVLGMSEGWSGPLAIAHG
VMADAIDVTPVKAALSALGAEAGEATIVLAKAEPSRSGRIRGKRHTMLDD
SDISPTRHARAFVAGALAGVVGHTEIYVSGGGEHQGPDGGGPVAVIAART
M
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
4nq3 Chain A Residue 409 [
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Receptor-Ligand Complex Structure
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PDB
4nq3
Cyanuric acid hydrolase from Azorhizobium caulinodans ORS 571: crystal structure and insights into a new class of Ser-Lys dyad proteins.
Resolution
2.702 Å
Binding residue
(original residue number in PDB)
E287 G336 Q339 G340 P341 G344
Binding residue
(residue number reindexed from 1)
E283 G332 Q335 G336 P337 G340
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:4nq3
,
PDBe:4nq3
,
PDBj:4nq3
PDBsum
4nq3
PubMed
24915109
UniProt
A8IKD2
|CAH_AZOC5 Cyanuric acid amidohydrolase (Gene Name=AZC_3892)
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