Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

1CP3

CRYSTAL STRUCTURE OF THE COMPLEX OF APOPAIN WITH THE TETRAPEPTIDE INHIBITOR ACE-DVAD-FMC

Summary for 1CP3
Entry DOI10.2210/pdb1cp3/pdb
Related PRD IDPRD_000239
DescriptorAPOPAIN, ACETYL-ASP-VAL-ALA-ASP-FLUOROMETHYLKETONE (3 entities in total)
Functional Keywordshydrolase-hydrolase inhibitor complex, apoptosis, interleukin-1beta-converting enzyme, cysteine-protease, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P42574
Total number of polymer chains4
Total formula weight64196.73
Authors
Mittl, P.R.E.,Dimarco, S.,Gruetter, M.G. (deposition date: 1996-12-12, release date: 1997-12-24, Last modification date: 2012-12-12)
Primary citationMittl, P.R.,Di Marco, S.,Krebs, J.F.,Bai, X.,Karanewsky, D.S.,Priestle, J.P.,Tomaselli, K.J.,Grutter, M.G.
Structure of recombinant human CPP32 in complex with the tetrapeptide acetyl-Asp-Val-Ala-Asp fluoromethyl ketone.
J.Biol.Chem., 272:6539-6547, 1997
Cited by
PubMed: 9045680
DOI: 10.1074/jbc.272.10.6539
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

217705

건을2024-03-27부터공개중

PDB statisticsPDBj update infoContact PDBjnumon