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4AXL

HUMAN CATHEPSIN L APO FORM WITH ZN

Summary for 4AXL
Entry DOI10.2210/pdb4axl/pdb
Related1CJL 1CS8 1ICF 1MHW 2VHS 2XU1 2XU3 2XU4 2XU5 2YJ2 2YJ8 2YJ9 2YJB 2YJC 4AXM
DescriptorCATHEPSIN L1, ZINC ION, GLYCEROL, ... (5 entities in total)
Functional Keywordshydrolase
Biological sourceHOMO SAPIENS (HUMAN)
Cellular locationLysosome: P07711
Total number of polymer chains1
Total formula weight24408.25
Authors
Banner, D.W.,Benz, J. (deposition date: 2012-06-13, release date: 2013-05-08, Last modification date: 2023-12-20)
Primary citationEhmke, V.,Winkler, E.,Banner, D.W.,Haap, W.,Schweizer, W.B.,Rottmann, M.,Kaiser, M.,Freymond, C.,Schirmeister, T.,Diederich, F.
Optimization of Triazine Nitriles as Rhodesain Inhibitors: Structure-Activity Relationships, Bioisosteric Imidazopyridine Nitriles, and X-Ray Crystal Structure Analysis with Human Cathepsin L
Chemmedchem, 8:967-, 2013
Cited by
PubMed: 23658062
DOI: 10.1002/CMDC.201300112
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.92 Å)
Structure validation

221051

數據於2024-06-12公開中

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