1APU
Crystallographic analysis of a pepstatin analogue binding to the aspartyl proteinase penicillopepsin at 1.8 angstroms resolution
Summary for 1APU
Entry DOI | 10.2210/pdb1apu/pdb |
Related | 1APT 1APV 1APW |
Related PRD ID | PRD_001238 |
Descriptor | PROTEIN (PENICILLOPEPSIN), PEPSTATIN ANALOGUE ISOVALERYL-VAL-VAL-STA-O-ET, alpha-D-mannopyranose, ... (4 entities in total) |
Functional Keywords | acid proteinase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Penicillium janthinellum |
Total number of polymer chains | 2 |
Total formula weight | 34134.62 |
Authors | Sielecki, A.R.,James, M.N.G. (deposition date: 1991-12-16, release date: 1994-01-31, Last modification date: 2024-10-16) |
Primary citation | James, 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
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