Structure of PDB 2icq Chain A Binding Site BS01
Receptor Information
>2icq Chain A (length=295) Species:
5059
(Aspergillus flavus) [
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SAVKAARYGKDNVRVYKVHKDEKTGVQTVYEMTVCVLLEGEIETSYTKAD
NSVIVATDSIKNTIYITAKQNPVTPPELFGSILGTHFIEKYNHIHAAHVN
IVCHRWTRMDIDGKPHPHSFIRDSEEKRNVQVDVVEGKGIDIKSSLSGLT
VLKSTNSQFWGFLRDEYTTLKETWDRILSTDVDATWQWKNFSGLQEVRSH
VPKFDATWATAREVTLKTFAEDNSASVQATMYKMAEQILARQQLIETVEY
SLPNKHYFEIDLSWHKGLQNTGKNAEVFAPQSDPNGLIKCTVGRS
Ligand information
Ligand ID
AZA
InChI
InChI=1S/C4H3N5O2/c10-3-1-2(8-9-7-1)5-4(11)6-3/h(H3,5,6,7,8,9,10,11)
InChIKey
KVGVQTOQSNJTJI-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
O=C1NC(=O)c2nn[nH]c2N1
OpenEye OEToolkits 1.5.0
c12c([nH]nn1)NC(=O)NC2=O
ACDLabs 10.04
O=C2Nc1nnnc1C(=O)N2
Formula
C4 H3 N5 O2
Name
8-AZAXANTHINE
ChEMBL
CHEMBL219341
DrugBank
DB01875
ZINC
ZINC000018123155
PDB chain
2icq Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
2icq
Protein Crystallography under Xenon and Nitrous Oxide Pressure: Comparison with In Vivo Pharmacology Studies and Implications for the Mechanism of Inhaled Anesthetic Action
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
F159 R176 S226 V227 Q228
Binding residue
(residue number reindexed from 1)
F159 R176 S226 V227 Q228
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
K10 T57 R176 Q228 H256
Catalytic site (residue number reindexed from 1)
K10 T57 R176 Q228 H256
Enzyme Commision number
1.7.3.3
: factor independent urate hydroxylase.
Gene Ontology
Molecular Function
GO:0004846
urate oxidase activity
GO:0016491
oxidoreductase activity
Biological Process
GO:0006144
purine nucleobase metabolic process
GO:0006145
purine nucleobase catabolic process
GO:0019628
urate catabolic process
Cellular Component
GO:0005777
peroxisome
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Molecular Function
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Cellular Component
External links
PDB
RCSB:2icq
,
PDBe:2icq
,
PDBj:2icq
PDBsum
2icq
PubMed
17028130
UniProt
Q00511
|URIC_ASPFL Uricase (Gene Name=uaZ)
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