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1APU

Crystallographic analysis of a pepstatin analogue binding to the aspartyl proteinase penicillopepsin at 1.8 angstroms resolution

Summary for 1APU
Entry DOI10.2210/pdb1apu/pdb
Related1APT 1APV 1APW
Related PRD IDPRD_001238
DescriptorPROTEIN (PENICILLOPEPSIN), PEPSTATIN ANALOGUE ISOVALERYL-VAL-VAL-STA-O-ET, alpha-D-mannopyranose, ... (4 entities in total)
Functional Keywordsacid proteinase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourcePenicillium janthinellum
Total number of polymer chains2
Total formula weight34134.62
Authors
Sielecki, A.R.,James, M.N.G. (deposition date: 1991-12-16, release date: 1994-01-31, Last modification date: 2020-07-29)
Primary citationJames, M.N.G.,Sielecki, A.R.,Moult, J.
Crystallographic Analysis of Transition State Mimics Bound to Penicillopepsin: Difluorostatine-and Difluorostatone-Containing Peptides
Biochemistry, 31:3872-, 1992
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

218853

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