Structure of PDB 1v2e Chain A Binding Site BS02
Receptor Information
>1v2e Chain A (length=368) Species:
274
(Thermus thermophilus) [
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MRLHPRTEAAKESIFPRMSGLAQRLGAVNLGQGFPSNPPPPFLLEAVRRA
LGRQDQYAPPAGLPALREALAEEFAVEPESVVVTSGATEALYVLLQSLVG
PGDEVVVLEPFFDVYLPDAFLAGAKARLVRLDLTPEGFRLDLSALEKALT
PRTRALLLNTPMNPTGLVFGERELEAIARLARAHDLFLISDEVYDELYYG
ERPRRLREFAPERTFTVGSAGKRLEATGYRVGWIVGPKEFMPRLAGMRQW
TSFSAPTPLQAGVAEALKLARREGFYEALREGYRRRRDLLAGGLRAMGLR
VYVPEGTYFLMAELPGWDAFRLVEEARVALIPASAFYLEDPPKDLFRFAF
CKTEEELHLALERLGRVV
Ligand information
Ligand ID
KMT
InChI
InChI=1S/C5H8O3S/c1-9-3-2-4(6)5(7)8/h2-3H2,1H3,(H,7,8)
InChIKey
SXFSQZDSUWACKX-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)C(=O)CCSC
CACTVS 3.341
CSCCC(=O)C(O)=O
OpenEye OEToolkits 1.5.0
CSCCC(=O)C(=O)O
Formula
C5 H8 O3 S
Name
4-(METHYLSULFANYL)-2-OXOBUTANOIC ACID
ChEMBL
CHEMBL1233860
DrugBank
DB02238
ZINC
ZINC000001532883
PDB chain
1v2e Chain A Residue 520 [
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Receptor-Ligand Complex Structure
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PDB
1v2e
Crystal structures of glutamine:phenylpyruvate aminotransferase from Thermus thermophilus HB8: induced fit and substrate recognition
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
F15 Q32 G33 F112 K222 F309 R347
Binding residue
(residue number reindexed from 1)
F15 Q32 G33 F112 K222 F309 R347
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
F112 A181 A183 K222
Catalytic site (residue number reindexed from 1)
F112 A181 A183 K222
Enzyme Commision number
2.6.1.15
: glutamine--pyruvate transaminase.
Gene Ontology
Molecular Function
GO:0008483
transaminase activity
GO:0016212
kynurenine-oxoglutarate transaminase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0009058
biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1v2e
,
PDBe:1v2e
,
PDBj:1v2e
PDBsum
1v2e
PubMed
14761974
UniProt
Q75WK2
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