Structure of PDB 3fvu Chain A Binding Site BS01
Receptor Information
>3fvu Chain A (length=419) Species:
9606
(Homo sapiens) [
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QLQARRLDGIDYNPWVEFVKLASEHDVVNLGQGFPDFPPPDFAVEAFQHA
VSGDFMLNQYTKTFGYPPLTKILASFFGELLGQEIDPLRNVLVTVGGYGA
LFTAFQALVDEGDEVIIIEPFFDCYEPMTMMAGGRPVFVSLKPGPIQNGE
LGSSSNWQLDPMELAGKFTSRTKALVLNTPNNPLGKVFSREELELVASLC
QQHDVVCITDEVYQWMVYDGHQHISIASLPGMWERTLTIGSAGKTFSATG
WKVGWVLGPDHIMKHLRTVHQNSVFHCPTQSQAAVAESFEREQLLFRQPS
SYFVQFPQAMQRCRDHMIRSLQSVGLKPIIPQGSYFLITDISDFKRKMPD
LPGAVDEPYDRRFVKWMIKNKGLVAIPVSIFYSVPHQKHFDHYIRFCFVK
DEATLQAMDEKLRKWKVEL
Ligand information
Ligand ID
IAC
InChI
InChI=1S/C10H9NO2/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H,12,13)
InChIKey
SEOVTRFCIGRIMH-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1ccc2c(c1)c(c[nH]2)CC(=O)O
ACDLabs 12.01
O=C(O)Cc2c1ccccc1nc2
CACTVS 3.370
OC(=O)Cc1c[nH]c2ccccc12
Formula
C10 H9 N O2
Name
1H-INDOL-3-YLACETIC ACID;
INDOLE ACETIC ACID
ChEMBL
CHEMBL82411
DrugBank
DB07950
ZINC
ZINC000000083860
PDB chain
3fvu Chain A Residue 423 [
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Receptor-Ligand Complex Structure
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PDB
3fvu
Structural insight into the inhibition of human kynurenine aminotransferase I/glutamine transaminase K
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
W18 G36 Y101 F125 X247 R398
Binding residue
(residue number reindexed from 1)
W15 G33 Y98 F122 X244 R395
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F125 D213 V215 K247
Catalytic site (residue number reindexed from 1)
F122 D210 V212 K244
Enzyme Commision number
2.6.1.64
: glutamine--phenylpyruvate transaminase.
2.6.1.7
: kynurenine--oxoglutarate transaminase.
4.4.1.13
: cysteine-S-conjugate beta-lyase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008483
transaminase activity
GO:0016212
kynurenine-oxoglutarate transaminase activity
GO:0016829
lyase activity
GO:0030170
pyridoxal phosphate binding
GO:0042803
protein homodimerization activity
GO:0047316
glutamine-phenylpyruvate transaminase activity
GO:0047804
cysteine-S-conjugate beta-lyase activity
Biological Process
GO:0009058
biosynthetic process
GO:0009617
response to bacterium
GO:0070189
kynurenine metabolic process
GO:0097053
L-kynurenine catabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3fvu
,
PDBe:3fvu
,
PDBj:3fvu
PDBsum
3fvu
PubMed
19338303
UniProt
Q16773
|KAT1_HUMAN Kynurenine--oxoglutarate transaminase 1 (Gene Name=KYAT1)
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