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Reaction Details
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TargetKynureninase
LigandBDBM50288255
Substrate/Competitorn/a
Meas. Tech.ChEBML_91720
Ki 4280±n/a nM
Citation Ross, FCBotting, NPLeeson, PD Synthesis of phosphinic acid transition state analogues for the reaction catalysed by kynureninase Bioorg Med Chem Lett6:2643-2646 (1996)    Article
More Info.:Get all data from this article,  Assay Method
 
Kynureninase
Name:Kynureninase
Synonyms:KYNU | KYNU_HUMAN | L-kynurenine hydrolase
Type:PROTEIN
Mol. Mass.:52356.52
Organism:Homo sapiens (Human)
Description:ChEMBL_91729
Residue:465
Sequence:
MEPSSLELPADTVQRIAAELKCHPTDERVALHLDEEDKLRHFRECFYIPKIQDLPPVDLS
LVNKDENAIYFLGNSLGLQPKMVKTYLEEELDKWAKIAAYGHEVGKRPWITGDESIVGLM
KDIVGANEKEIALMNALTVNLHLLMLSFFKPTPKRYKILLEAKAFPSDHYAIESQLQLHG
LNIEESMRMIKPREGEETLRIEDILEVIEKEGDSIAVILFSGVHFYTGQHFNIPAITKAG
QAKGCYVGFDLAHAVGNVELYLHDWGVDFACWCSYKYLNAGAGGIAGAFIHEKHAHTIKP
ALVGWFGHELSTRFKMDNKLQLIPGVCGFRISNPPILLVCSLHASLEIFKQATMKALRKK
SVLLTGYLEYLIKHNYGKDKAATKKPVVNIITPSHVEERGCQLTITFSVPNKDVFQELEK
RGVVCDKRNPNGIRVAPVPLYNSFHDVYKFTNLLTSILDSAETKN
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50288255
n/a
NameBDBM50288255
Synonyms:2-ammonio-4-(2-ammoniophenyl)-4-oxo-(2S)-butanoate
TypeSmall organic molecule
Emp. Form.C10H13N2O3
Mol. Mass.209.2213
SMILES[NH3+][C@@H](CC(=O)c1ccccc1[NH3+])C([O-])=O
Structure
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