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<Asymmetric unit>
= <Biological unit>

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PDB ID2bdl  sequence information (FASTA format)   
DescriptorCathepsin K (E.C.3.4.22.38)
TitleCathepsin K complexed with a pyrrolidine ketoamide-based inhibitor
Functional Keywordscathepsin, cysteine protease, catK, catO, HYDROLASE
Biological sourceHomo sapiens (human)
Cellular location [UNP - P43235] Lysosome
Organ source [UNP - P43235] Blood
[UNP - P43235] Bone
[UNP - P43235] Osteoclastoma
[UNP - P43235] Spleen
[UNP - P43235] Skin
Total number of polymer chains1
Total molecular weight24067.3 (the details in Structural Details Page)
AuthorsShewchuk, L.M. (deposition date : 2005-10-20, release date : 2006-03-21)
Primary citationBarrett, D.G. , Catalano, J.G. , Deaton, D.N. , Hassell, A.M. , Long, S.T. , Miller, A.B. , Miller, L.R. , Ray, J.A. , Samano, V. , Shewchuk, L.M. , Wells-Knecht, K.J. , Willard Jr., D.H. , Wright, L.L.
Novel, potent P2-P3 pyrrolidine derivatives of ketoamide-based cathepsin K inhibitors.
Bioorg.Med.Chem.Lett., 16:1735 - 1739, 2006.(PubMed : 16376075)  (DOI: 10.1016/j.bmcl.2005.11.101)
Experimental methodX-RAY DIFFRACTION ( 2.0[Å] )
Other Database Information
Yorodumi , CATH , CE , FSSP , SCOP , VAST , UniProt ( P43235 ) , eF-site , KEGG ( EC 3.4.22.38 ) , PISA