Structure of PDB 4knv Chain A Binding Site BS02

Receptor Information
>4knv Chain A (length=241) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MRAVFFDLDNTLIDTAGASRRGMLEVIKLLQSKYHYKEEAEIICDKVQVK
LSKECFHPYNTCITDLRTSHWEEAIQETKGGAANRKLAEECYFLWKSTRL
QHMTLAEDVKAMLTELRKEVRLLLLTNGDRQTQREKIEACACQSYFDAVV
VGGEQREEKPAPSIFYYCCNLLGVQPGDCVMVGDTLETDIQGGLNAGLKA
TVWINKNGIVPLKSSPVPHYMVSSVLELPALLQSIDCLVPR
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 chain4knv Chain A Residue 302 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB4knv Design, synthesis, functional and structural characterization of an inhibitor of N-acetylneuraminate-9-phosphate phosphatase: Observation of extensive dynamics in an enzyme/inhibitor complex.
Resolution1.993 Å
Binding residue
(original residue number in PDB)
D12 D14 D189
Binding residue
(residue number reindexed from 1)
D7 D9 D184
Annotation score1
Enzymatic activity
Enzyme Commision number 3.1.3.29: N-acylneuraminate-9-phosphatase.
Gene Ontology
Molecular Function
GO:0016787 hydrolase activity
GO:0016791 phosphatase activity
GO:0050124 N-acylneuraminate-9-phosphatase activity
Biological Process
GO:0006045 N-acetylglucosamine biosynthetic process
GO:0006055 CMP-N-acetylneuraminate biosynthetic process
GO:0044283 small molecule biosynthetic process
GO:0046380 N-acetylneuraminate biosynthetic process
GO:0070085 glycosylation
Cellular Component
GO:0005575 cellular_component
GO:0005829 cytosol

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Biological Process

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Cellular Component
External links
PDB RCSB:4knv, PDBe:4knv, PDBj:4knv
PDBsum4knv
PubMed23747226
UniProtQ8TBE9|NANP_HUMAN N-acylneuraminate-9-phosphatase (Gene Name=NANP)

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