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1YT7

Cathepsin K complexed with a constrained ketoamide inhibitor

Summary for 1YT7
Entry DOI10.2210/pdb1yt7/pdb
Related1TU6
DescriptorCathepsin K, SULFATE ION, (1R)-2,2-DIMETHYL-1-({5-[4-(TRIFLUOROMETHYL)PHENYL]-1,3,4-OXADIAZOL-2-YL}METHYL)PROPYL (1S)-1-{OXO[(2-OXO-1,3-OXAZOLIDIN-3-YL)AMINO]ACETYL}PENTYLCARBAMATE, ... (4 entities in total)
Functional Keywordscathepsin, cysteine protease, hydrolase
Biological sourceHomo sapiens (human)
Cellular locationLysosome: P43235
Total number of polymer chains1
Total formula weight24299.16
Authors
Primary citationBarrett, D.G.,Boncek, V.M.,Catalano, J.G.,Deaton, D.N.,Hassell, A.M.,Jurgensen, C.H.,Long, S.T.,McFadyen, R.B.,Miller, A.B.,Miller, L.R.,Payne, J.A.,Ray, J.A.,Samano, V.,Shewchuk, L.M.,Tavares, F.X.,Wells-Knecht, K.J.,Willard, D.H.,Wright, L.L.,Zhou, H.Q.
P(2)-P(3) conformationally constrained ketoamide-based inhibitors of cathepsin K.
Bioorg.Med.Chem.Lett., 15:3540-3546, 2005
Cited by
PubMed: 15982880
DOI: 10.1016/j.bmcl.2005.05.062
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

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