Structure of PDB 3av7 Chain C Binding Site BS03
Receptor Information
>3av7 Chain C (length=404) Species:
70601
(Pyrococcus horikoshii OT3) [
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SMLGDVERFFSKKALEMRASEVRELLKLVETSDIISLAGGLPNPKTFPKE
IIRDILVEIMEKYADKALQYGTTKGFTPLRETLMKWLGKRYGISQDNDIM
ITSGSQQALDLIGRVFLNPGDIVVVEAPTYLAALQAFNFYEPQYIQIPLD
DEGMKVEILEEKLKELKSQGKKVKVVYTVPTFQNPAGVTMNEDRRKYLLE
LASEYDFIVVEDDPYGELRYSGNPEKKIKALDNEGRVIYLGTFSKILAPG
FRIGWMVGDPGIIRKMEIAKQSTDLCTNVFGQVVAWRYVDGGYLEKHIPE
IRKFYKPRRDAMLEALEEFMPEGVKWTKPEGGMFIWVTLPDGIDSKKMLE
RAIKKGVAYVPGEAFYAHRDVKNTMRLNFTYVDEDKIMEGIKRLAETIKE
ELKA
Ligand information
Ligand ID
KYA
InChI
InChI=1S/C10H7NO3/c12-9-5-8(10(13)14)11-7-4-2-1-3-6(7)9/h1-5H,(H,11,12)(H,13,14)
InChIKey
HCZHHEIFKROPDY-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
OC(=O)c1cc(O)c2ccccc2n1
ACDLabs 12.01
O=C(O)c1nc2ccccc2c(O)c1
OpenEye OEToolkits 1.7.0
c1ccc2c(c1)c(cc(n2)C(=O)O)O
Formula
C10 H7 N O3
Name
4-hydroxyquinoline-2-carboxylic acid;
Kynurenic acid
ChEMBL
CHEMBL299155
DrugBank
DB11937
ZINC
ZINC000008584773
PDB chain
3av7 Chain C Residue 431 [
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Receptor-Ligand Complex Structure
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PDB
3av7
Structural insight into kynurenic acid excretion mechanisms of kynurenine aminotransferase in the hyperthermophilic archaeon Pyrococcus horikoshii
Resolution
1.84 Å
Binding residue
(original residue number in PDB)
S44 V46 R47 L155 Q159 A388 R393
Binding residue
(residue number reindexed from 1)
S20 V22 R23 L131 Q135 A364 R369
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.6.1.7
: kynurenine--oxoglutarate transaminase.
Gene Ontology
Molecular Function
GO:0008483
transaminase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0009058
biosynthetic process
GO:1901605
alpha-amino acid metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3av7
,
PDBe:3av7
,
PDBj:3av7
PDBsum
3av7
PubMed
UniProt
O57946
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