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Structure paper

TitleDesigning Smac-mimetics as antagonists of XIAP, cIAP1, and cIAP2.
Journal, issue, pagesBiochem. Biophys. Res. Commun., Vol. 378, Page 162-167, Year 2009
Publish dateOct 21, 2008 (structure data deposition date)
AuthorsCossu, F. / Mastrangelo, E. / Milani, M. / Sorrentino, G. / Lecis, D. / Delia, D. / Manzoni, L. / Seneci, P. / Scolastico, C. / Bolognesi, M.
External linksBiochem. Biophys. Res. Commun. / PubMed:18992220
MethodsX-ray diffraction
Resolution3 Å
Structure data

PDB-3eyl:
Crystal structure of XIAP BIR3 domain in complex with a Smac-mimetic compound
Method: X-RAY DIFFRACTION / Resolution: 3 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-SMK:
(3S,6S,7R,9aS)-6-{[(2S)-2-aminobutanoyl]amino}-7-(2-aminoethyl)-N-(diphenylmethyl)-5-oxooctahydro-1H-pyrrolo[1,2-a]azepine-3-carboxamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsLIGASE / Apoptosis / Smac-mimetics / Zinc-finger / Metal-binding / Phosphoprotein / Protease inhibitor / Thiol protease inhibitor / Ubl conjugation pathway

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