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1RHK

Crystal structure of the complex of caspase-3 with a phenyl-propyl-ketone inhibitor

Summary for 1RHK
Entry DOI10.2210/pdb1rhk/pdb
Related1PAU 1RHJ 1RHM 1RHQ 1RHR 1RHU
Related PRD IDPRD_000231
DescriptorCaspase-3, acetyl-asp-glu-val-fpr, ... (4 entities in total)
Functional Keywordscysteine protease, caspase-3, apopain, cpp32, yama, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (human)
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Cellular locationCytoplasm: P42574 P42574
Total number of polymer chains3
Total formula weight29155.15
Authors
Becker, J.W.,Rotonda, J.,Soisson, S.M. (deposition date: 2003-11-14, release date: 2004-05-11, Last modification date: 2023-09-20)
Primary citationBecker, J.W.,Rotonda, J.,Soisson, S.M.,Aspiotis, R.,Bayly, C.,Francoeur, S.,Gallant, M.,Garcia-Calvo, M.,Giroux, A.,Grimm, E.,Han, Y.,McKay, D.,Nicholson, D.W.,Peterson, E.,Renaud, J.,Roy, S.,Thornberry, N.,Zamboni, R.
Reducing the Peptidyl Features of Caspase-3 Inhibitors: A Structural Analysis.
J.Med.Chem., 47:2466-2474, 2004
Cited by
PubMed: 15115390
DOI: 10.1021/jm0305523
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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