2o2k
From Proteopedia
Contents |
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 Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Crystal structure and solution characterization of the activation domain of human methionine synthase., Wolthers KR, Toogood HS, Jowitt TA, Marshall KR, Leys D, Scrutton NS, FEBS J. 2007 Feb;274(3):738-50. PMID:17288554
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