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4HY5

Crystal structure of cIAP1 BIR3 bound to T3256336

Summary for 4HY5
Entry DOI10.2210/pdb4hy5/pdb
Related4HY0 4HY4
Related PRD IDPRD_001138
DescriptorBaculoviral IAP repeat-containing protein 2, ZINC ION, (3S,7R,8aR)-2-{(2S)-2-(4,4-difluorocyclohexyl)-2-[(N-methyl-L-alanyl)amino]acetyl}-N-[(4R)-3,4-dihydro-2H-chromen-4-yl]-7-ethoxyoctahydropyrrolo[1,2-a]pyrazine-3-carboxamide, ... (4 entities in total)
Functional Keywordsiap family, bir repeats, card domain, ring-type zinc finger, ligase-ligase inhibitor complex, ligase/ligase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: Q13490
Total number of polymer chains2
Total formula weight27931.91
Authors
Dougan, D.R.,Snell, G.P. (deposition date: 2012-11-13, release date: 2013-01-30, Last modification date: 2024-02-28)
Primary citationHashimoto, K.,Saito, B.,Miyamoto, N.,Oguro, Y.,Tomita, D.,Shiokawa, Z.,Asano, M.,Kakei, H.,Taya, N.,Kawasaki, M.,Sumi, H.,Yabuki, M.,Iwai, K.,Yoshida, S.,Yoshimatsu, M.,Aoyama, K.,Kosugi, Y.,Kojima, T.,Morishita, N.,Dougan, D.R.,Snell, G.P.,Imamura, S.,Ishikawa, T.
Design and Synthesis of Potent Inhibitor of Apoptosis (IAP) Proteins Antagonists Bearing an Octahydropyrrolo[1,2-a]pyrazine Scaffold as a Novel Proline Mimetic.
J.Med.Chem., 56:1228-1246, 2013
Cited by
PubMed: 23298277
DOI: 10.1021/jm301674z
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.752 Å)
Structure validation

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