Structure of PDB 2rdu Chain A Binding Site BS02
Receptor Information
>2rdu Chain A (length=360) Species:
9606
(Homo sapiens) [
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PRLICINDYEQHAKSVLPKSIYDYYRSGANDEETLADNIAAFSRWKLYPR
MLRNVAETDLSTSVLGQRVSMPICVGATAMQRMAHVDGELATVRACQSLG
TGMMLSSWATSSIEEVAEAGPEALRWLQLYIYKDREVTKKLVRQAEKMGY
KAIFVTVDTPYLGNRLDDVRNRFKLPPQLRMKNFETSTLSFSPEENFGDD
SGLAAYVAKAIDPSISWEDIKWLRRLTSLPIVAKGILRGDDAREAVKHGL
NGILVSNHGARQLDGVPATIDVLPEIVEAVEGKVEVFLDGGVRKGTDVLK
ALALGAKAVFVGRPIVWGLAFQGEKGVQDVLEILKEEFRLAMALSGCQNV
KVIDKTLVRK
Ligand information
Ligand ID
GLV
InChI
InChI=1S/C2H2O3/c3-1-2(4)5/h1H,(H,4,5)
InChIKey
HHLFWLYXYJOTON-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)C(=O)O
ACDLabs 10.04
O=CC(=O)O
CACTVS 3.341
OC(=O)C=O
Formula
C2 H2 O3
Name
GLYOXYLIC ACID;
GLYOXALATE;
GLYOXYLATE
ChEMBL
CHEMBL1162545
DrugBank
DB04343
ZINC
ZINC000004658554
PDB chain
2rdu Chain A Residue 372 [
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Receptor-Ligand Complex Structure
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PDB
2rdu
Active Site and Loop 4 Movements within Human Glycolate Oxidase: Implications for Substrate Specificity and Drug Design.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
Y26 W110 Y132 R167 H260 R263
Binding residue
(residue number reindexed from 1)
Y24 W108 Y130 R165 H258 R261
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
S108 Y132 T158 D160 K236 H260
Catalytic site (residue number reindexed from 1)
S106 Y130 T156 D158 K234 H258
Enzyme Commision number
1.1.3.15
: (S)-2-hydroxy-acid oxidase.
1.2.3.5
: glyoxylate oxidase.
Gene Ontology
Molecular Function
GO:0003973
(S)-2-hydroxy-acid oxidase activity
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0047969
glyoxylate oxidase activity
Biological Process
GO:0001561
fatty acid alpha-oxidation
GO:0006545
glycine biosynthetic process
GO:0006979
response to oxidative stress
GO:0008652
amino acid biosynthetic process
GO:0046296
glycolate catabolic process
Cellular Component
GO:0005777
peroxisome
GO:0005782
peroxisomal matrix
GO:0005829
cytosol
GO:0043231
intracellular membrane-bounded organelle
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2rdu
,
PDBe:2rdu
,
PDBj:2rdu
PDBsum
2rdu
PubMed
18215067
UniProt
Q9UJM8
|HAOX1_HUMAN 2-Hydroxyacid oxidase 1 (Gene Name=HAO1)
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