Structure of PDB 4nq3 Chain A Binding Site BS02

Receptor Information
>4nq3 Chain A (length=351) Species: 438753 (Azorhizobium caulinodans ORS 571) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MPIAKVHRIATASPDDVSGLAAAIATGAIAPAGILAIFGKTEGNGCVNDF
SRGFAVQSLQMLLRGHMGAAADEVCLVMSGGTEGGMSPHFLVFERAEGNA
PALAIGRAHTPDLPFEALGRMGQVRMVAQAVRRAMAAAGITDPEDVHFVQ
VKCPLLTAMRVKEAEARGATTATSDTLKSMGLSRGASALGIALALGEVAE
DALSDAVICADYGLWSARASCSSGIELLGHEIVVLGMSEGWSGPLAIAHG
VMADAIDVTPVKAALSALGAEAGEATIVLAKAEPSRSGRIRGKRHTMLDD
SDISPTRHARAFVAGALAGVVGHTEIYVSGGGEHQGPDGGGPVAVIAART
M
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 chain4nq3 Chain A Residue 409 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB4nq3 Cyanuric acid hydrolase from Azorhizobium caulinodans ORS 571: crystal structure and insights into a new class of Ser-Lys dyad proteins.
Resolution2.702 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 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:4nq3, PDBe:4nq3, PDBj:4nq3
PDBsum4nq3
PubMed24915109
UniProtA8IKD2|CAH_AZOC5 Cyanuric acid amidohydrolase (Gene Name=AZC_3892)

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