This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
1tu6
From Proteopedia
(Difference between revisions)
m (Protected "1tu6" [edit=sysop:move=sysop]) |
|||
| Line 1: | Line 1: | ||
[[Image:1tu6.png|left|200px]] | [[Image:1tu6.png|left|200px]] | ||
| - | <!-- | ||
| - | The line below this paragraph, containing "STRUCTURE_1tu6", 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_1tu6| PDB=1tu6 | SCENE= }} | {{STRUCTURE_1tu6| PDB=1tu6 | SCENE= }} | ||
===Cathepsin K complexed with a ketoamide inhibitor=== | ===Cathepsin K complexed with a ketoamide inhibitor=== | ||
| - | |||
| - | <!-- | ||
| - | The line below this paragraph, {{ABSTRACT_PUBMED_15341947}}, adds the Publication Abstract to the page | ||
| - | (as it appears on PubMed at http://www.pubmed.gov), where 15341947 is the PubMed ID number. | ||
| - | --> | ||
{{ABSTRACT_PUBMED_15341947}} | {{ABSTRACT_PUBMED_15341947}} | ||
| Line 22: | Line 11: | ||
==See Also== | ==See Also== | ||
| - | *[[Cathepsin]] | + | *[[Cathepsin|Cathepsin]] |
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:015341947</ref><references group="xtra"/> |
[[Category: Cathepsin K]] | [[Category: Cathepsin K]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
Revision as of 17:30, 25 July 2012
Contents |
Cathepsin K complexed with a ketoamide inhibitor
Template:ABSTRACT PUBMED 15341947
About this Structure
1tu6 is a 2 chain structure of Cathepsin with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Barrett DG, Catalano JG, Deaton DN, Hassell AM, Long ST, Miller AB, Miller LR, Shewchuk LM, Wells-Knecht KJ, Willard DH Jr, Wright LL. Potent and selective P2-P3 ketoamide inhibitors of cathepsin K with good pharmacokinetic properties via favorable P1', P1, and/or P3 substitutions. Bioorg Med Chem Lett. 2004 Oct 4;14(19):4897-902. PMID:15341947 doi:10.1016/j.bmcl.2004.07.031
