We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

2qfm

From Proteopedia

Revision as of 21:26, 12 November 2007 by OCA (Talk | contribs)
(diff) ←Older revision | Current revision (diff) | Newer revision→ (diff)
Jump to: navigation, search
Image:2qfm.gif

2qfm, resolution 1.80Å

Drag the structure with the mouse to rotate

Crystal structure of human spermine synthase in complex with spermidine and 5-methylthioadenosine

Disease

Known diseases associated with this structure: Mental retardation, X-linked, Snyder-Robinson type OMIM:[300105], Smith-Magenis syndrome OMIM:[607642]

About this Structure

2QFM is a Single protein structure of sequence from Homo sapiens with SPD and MTA as ligands. Active as Spermine synthase, with EC number 2.5.1.22 Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Nov 12 23:32:51 2007

Proteopedia Page Contributors and Editors (what is this?)

OCA

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