2r6n
From Proteopedia
Line 1: | Line 1: | ||
[[Image:2r6n.jpg|left|200px]] | [[Image:2r6n.jpg|left|200px]] | ||
- | + | <!-- | |
- | + | The line below this paragraph, containing "STRUCTURE_2r6n", creates the "Structure Box" on the page. | |
- | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
- | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
- | + | or leave the SCENE parameter empty for the default display. | |
- | + | --> | |
- | + | {{STRUCTURE_2r6n| PDB=2r6n | SCENE= }} | |
- | + | ||
- | + | ||
- | }} | + | |
'''Crystal structure of a pyrrolopyrimidine inhibitor in complex with human Cathepsin K''' | '''Crystal structure of a pyrrolopyrimidine inhibitor in complex with human Cathepsin K''' | ||
Line 30: | Line 27: | ||
[[Category: Mathis, B.]] | [[Category: Mathis, B.]] | ||
[[Category: Ramage, P.]] | [[Category: Ramage, P.]] | ||
- | [[Category: | + | [[Category: Covalent bond to inhibitor]] |
- | [[Category: | + | [[Category: Disease mutation]] |
- | [[Category: | + | [[Category: Glycoprotein]] |
- | [[Category: | + | [[Category: Hydrolase]] |
- | [[Category: | + | [[Category: Lysosome]] |
- | [[Category: | + | [[Category: Protease]] |
- | [[Category: | + | [[Category: Thiol protease]] |
- | [[Category: | + | [[Category: Zymogen]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 16:20:09 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 13:20, 4 May 2008
Crystal structure of a pyrrolopyrimidine inhibitor in complex with human Cathepsin K
Overview
Pyrrolopyrimidine, a novel scaffold, allows to adjust interactions within the S3 subsite of cathepsin K. The core intermediate 10 facilitated the P3 optimization and identified highly potent and selective cathepsin K inhibitors 11-20.
About this Structure
2R6N is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Novel scaffold for cathepsin K inhibitors., Teno N, Miyake T, Ehara T, Irie O, Sakaki J, Ohmori O, Gunji H, Matsuura N, Masuya K, Hitomi Y, Nonomura K, Horiuchi M, Gohda K, Iwasaki A, Umemura I, Tada S, Kometani M, Iwasaki G, Cowan-Jacob SW, Missbach M, Lattmann R, Betschart C, Bioorg Med Chem Lett. 2007 Nov 15;17(22):6096-100. Epub 2007 Sep 15. PMID:17911019 Page seeded by OCA on Sun May 4 16:20:09 2008