2o2k | pdb_00002o2k
From Proteopedia
Crystal Structure of the Activation Domain of Human Methionine Synthase Isoform/Mutant D963E/K1071N
Template:ABSTRACT PUBMED 17288554
Disease
Known disease associated with this structure: Methylcobalamin deficiency, cblG type OMIM:[156570], Cleft lip/palate, susceptibility to OMIM:[156570], Down syndrome, susceptibility to OMIM:[156570], Neural tube defects, folate-sensitive, susceptibility to OMIM:[156570]
About this Structure
2O2K is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Wolthers KR, Toogood HS, Jowitt TA, Marshall KR, Leys D, Scrutton NS. Crystal structure and solution characterization of the activation domain of human methionine synthase. FEBS J. 2007 Feb;274(3):738-50. PMID:17288554 doi:10.1111/j.1742-4658.2006.05618.x
Page seeded by OCA on Tue Feb 17 03:49:22 2009
