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TargetE3 ubiquitin-protein ligase XIAP
LigandBDBM44280
Substrate/Competitorn/a
Meas. Tech.SAR analysis of Antagonists of IAP-family anti-apoptotic proteins
IC50 17500±3500 nM
Citation PubChem, PC SAR analysis of Antagonists of IAP-family anti-apoptotic proteins PubChem Bioassay(2009)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
E3 ubiquitin-protein ligase XIAP
Name:E3 ubiquitin-protein ligase XIAP
Synonyms:API3 | BIRC4 | E3 ubiquitin-protein ligase XIAP | IAP3 | Inhibitor of apoptosis protein 3 | Inhibitor of apoptosis protein 3 (XIAP) | X-linked inhibitor of apoptosis | X-linked inhibitor of apoptosis protein (XIAP) | XIAP | XIAP_HUMAN
Type:Protein
Mol. Mass.:56685.27
Organism:Homo sapiens (Human)
Description:P98170
Residue:497
Sequence:
MTFNSFEGSKTCVPADINKEEEFVEEFNRLKTFANFPSGSPVSASTLARAGFLYTGEGDT
VRCFSCHAAVDRWQYGDSAVGRHRKVSPNCRFINGFYLENSATQSTNSGIQNGQYKVENY
LGSRDHFALDRPSETHADYLLRTGQVVDISDTIYPRNPAMYSEEARLKSFQNWPDYAHLT
PRELASAGLYYTGIGDQVQCFCCGGKLKNWEPCDRAWSEHRRHFPNCFFVLGRNLNIRSE
SDAVSSDRNFPNSTNLPRNPSMADYEARIFTFGTWIYSVNKEQLARAGFYALGEGDKVKC
FHCGGGLTDWKPSEDPWEQHAKWYPGCKYLLEQKGQEYINNIHLTHSLEECLVRTTEKTP
SLTRRIDDTIFQNPMVQEAIRMGFSFKDIKKIMEEKIQISGSNYKSLEVLVADLVNAQKD
SMQDESSQTSLQKEISTEEQLRRLQEEKLCKICMDRNIAIVFVPCGHLVTCKQCAEAVDK
CPMCYTVITFKQKIFMS
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  Blast E-value cutoff:
BDBM44280
n/a
NameBDBM44280
Synonyms:(2S)-1-[(2S)-2-[[(2S)-2-amino-1-oxopropyl]amino]-2-cyclohexyl-1-oxoethyl]-2-pyrrolidinecarboxylic acid (phenylmethyl) ester;2,2,2-trifluoroacetic acid | (2S)-1-[(2S)-2-[[(2S)-2-aminopropanoyl]amino]-2-cyclohexyl-acetyl]pyrrolidine-2-carboxylic acid benzyl ester;2,2,2-trifluoroacetic acid | (phenylmethyl) (2S)-1-[(2S)-2-[[(2S)-2-azanylpropanoyl]amino]-2-cyclohexyl-ethanoyl]pyrrolidine-2-carboxylate;2,2,2-tris(fluoranyl)ethanoic acid | MLS-0390978.0001 | benzyl (2S)-1-[(2S)-2-[[(2S)-2-aminopropanoyl]amino]-2-cyclohexylacetyl]pyrrolidine-2-carboxylate;2,2,2-trifluoroacetic acid | cid_25241685
TypeSmall organic molecule
Emp. Form.C23H33N3O4
Mol. Mass.415.5258
SMILESC[C@H](N)C(=O)N[C@@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)OCc1ccccc1
Structure
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