3bic: Difference between revisions
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{{ABSTRACT_PUBMED_20876572}} | |||
==About this Structure== | ==About this Structure== | ||
[[3bic]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3BIC OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:020876572</ref><references group="xtra"/> | |||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Methylmalonyl-CoA mutase]] | [[Category: Methylmalonyl-CoA mutase]] | ||
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[[Category: Mitochondrion]] | [[Category: Mitochondrion]] | ||
[[Category: Organic aciduria]] | [[Category: Organic aciduria]] | ||
[[Category: Sgc]] | [[Category: Sgc]] | ||
[[Category: Structural genomic]] | [[Category: Structural genomic]] | ||
[[Category: Structural genomics consortium]] | [[Category: Structural genomics consortium]] | ||
[[Category: Transit peptide]] | [[Category: Transit peptide]] | ||
Revision as of 05:32, 14 September 2011
Crystal structure of human methylmalonyl-CoA mutase
Template:ABSTRACT PUBMED 20876572
About this Structure
3bic is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Froese DS, Kochan G, Muniz J, Wu X, Gileadi C, Ugochukwu E, Krysztofinska E, Gravel RA, Oppermann U, Yue WW. Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-coa mutase and insight into their complex formation. J Biol Chem. 2010 Sep 28. PMID:20876572 doi:10.1074/jbc.M110.177717
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Methylmalonyl-CoA mutase
- Arrowsmith, C H.
- Delft, F von.
- Edwards, A M.
- Gileadi, O.
- Kochan, G.
- Oppermann, U.
- Pantic, N.
- Parizotto, E.
- Pike, A C.W.
- Pilka, E S.
- SGC, Structural Genomics Consortium.
- Ugochukwu, E.
- Weigelt, J.
- Cobalamin
- Cobalt
- Disease mutation
- Isomerase
- Metabolic disease
- Metal-binding
- Methylmalonyl coa mutase deficiency
- Mitochondrion
- Organic aciduria
- Sgc
- Structural genomic
- Structural genomics consortium
- Transit peptide