2idx: Difference between revisions
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{{STRUCTURE_2idx| PDB=2idx | SCENE= }} | {{STRUCTURE_2idx| PDB=2idx | SCENE= }} | ||
===Structure of Human ATP:Cobalamin adenosyltransferase bound to ATP.=== | ===Structure of Human ATP:Cobalamin adenosyltransferase bound to ATP.=== | ||
{{ABSTRACT_PUBMED_17176040}} | |||
==Disease== | |||
[[http://www.uniprot.org/uniprot/MMAB_HUMAN MMAB_HUMAN]] Defects in MMAB are the cause of methylmalonic aciduria type cblB (MMAB) [MIM:[http://omim.org/entry/251110 251110]]; also known as methylmalonic aciduria type B or vitamin B12-responsive methylmalonicaciduria of cblB complementation type. MMAB is a disorder of methylmalonate and cobalamin metabolism due to defective synthesis of adenosylcobalamin. Inheritance is autosomal recessive.<ref>PMID:12471062</ref><ref>PMID:12514191</ref><ref>PMID:15781192</ref> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:017176040</ref><references group="xtra"/> | <ref group="xtra">PMID:017176040</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Hill, C P.]] | [[Category: Hill, C P.]] | ||
