2oxw

From Proteopedia

(Difference between revisions)
Jump to: navigation, search

OCA (Talk | contribs)
(New page: 200px<br /> <applet load="2oxw" size="450" color="white" frame="true" align="right" spinBox="true" caption="2oxw, resolution 1.15&Aring;" /> '''Human MMP-12 comple...)
Next diff →

Revision as of 21:11, 12 November 2007

Image:2oxw.gif

2oxw, resolution 1.15Å

Drag the structure with the mouse to rotate

Human MMP-12 complexed with the peptide IAG

Disease

Known diseases associated with this structure: Cardiomyopathy, dilated, 1G OMIM:[188840], Cardiomyopathy, familial hypertrophic OMIM:[188840], Muscular dystrophy, limb-girdle, type 2J OMIM:[188840], Myopathy, proximal, with early respiratory muscle involvement OMIM:[188840], Tibial muscular dystrophy, tardive OMIM:[188840]

About this Structure

2OXW is a Single protein structure of sequence from Homo sapiens with ZN and CA as ligands. Active as Macrophage elastase, with EC number 3.4.24.65 Full crystallographic information is available from OCA.

Reference

Snapshots of the reaction mechanism of matrix metalloproteinases., Bertini I, Calderone V, Fragai M, Luchinat C, Maletta M, Yeo KJ, Angew Chem Int Ed Engl. 2006 Dec 4;45(47):7952-5. PMID:17096442

Page seeded by OCA on Mon Nov 12 23:17:58 2007

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/2oxw"
Personal tools