Structure of PDB 2pes Chain A Binding Site BS02
Receptor Information
>2pes Chain A (length=295) Species:
5059
(Aspergillus flavus) [
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SAVKAARYGKDNVRVYKVHKDEKTGVQTVYEMTVCVLLEGEIETSYTKAD
NSVIVATDSIKNTIYITAKQNPVTPPELFGSILGTHFIEKYNHIHAAHVN
IVCHRWTRMDIDGKPHPHSFIRDSEEKRNVQVDVVEGKGIDIKSSLSGLT
VLKSTNSQFWGFLRDEYTTLKETWDRILSTDVDATWQWKNFSGLQEVRSH
VPKFDATWATAREVTLKTFAEDNSASVQATMYKMAEQILARQQLIETVEY
SLPNKHYFEIDLSWHKGLQNTGKNAEVFAPQSDPNGLIKCTVGRS
Ligand information
Ligand ID
PDC
InChI
InChI=1S/C7H5NO4/c9-6(10)4-2-1-3-5(8-4)7(11)12/h1-3H,(H,9,10)(H,11,12)
InChIKey
WJJMNDUMQPNECX-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)c1nc(C(=O)O)ccc1
CACTVS 3.341
OC(=O)c1cccc(n1)C(O)=O
OpenEye OEToolkits 1.5.0
c1cc(nc(c1)C(=O)O)C(=O)O
Formula
C7 H5 N O4
Name
PYRIDINE-2,6-DICARBOXYLIC ACID;
DIPICOLINIC ACID
ChEMBL
CHEMBL284104
DrugBank
DB04267
ZINC
ZINC000000105246
PDB chain
2pes Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
2pes
A dipicolinate lanthanide complex for solving protein structures using anomalous diffraction.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
P202 K203 A206 Q242
Binding residue
(residue number reindexed from 1)
P202 K203 A206 Q242
Annotation score
1
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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Biological Process
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Cellular Component
External links
PDB
RCSB:2pes
,
PDBe:2pes
,
PDBj:2pes
PDBsum
2pes
PubMed
20606256
UniProt
Q00511
|URIC_ASPFL Uricase (Gene Name=uaZ)
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