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Reaction Details
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TargetKynureninase
LigandBDBM50288258
Substrate/Competitorn/a
Meas. Tech.ChEBML_91720
Ki 880000±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
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  Blast E-value cutoff:
BDBM50288258
n/a
NameBDBM50288258
Synonyms:(R)-2-Benzyloxycarbonylamino-3-(methoxy-phenyl-phosphinoyl)-propionic acid | CHEMBL85072
TypeSmall organic molecule
Emp. Form.C18H20NO6P
Mol. Mass.377.3283
SMILESCOP(=O)(C[C@H](NC(=O)OCc1ccccc1)C(O)=O)c1ccccc1
Structure
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