3bic: Difference between revisions
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[[Image:3bic.jpg|left|200px]] | [[Image:3bic.jpg|left|200px]] | ||
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| | {{STRUCTURE_3bic| PDB=3bic | SCENE= }} | ||
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'''Crystal structure of human methylmalonyl-CoA mutase''' | '''Crystal structure of human methylmalonyl-CoA mutase''' | ||
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[[Category: Ugochukwu, E.]] | [[Category: Ugochukwu, E.]] | ||
[[Category: Weigelt, J.]] | [[Category: Weigelt, J.]] | ||
[[Category: | [[Category: Cobalamin]] | ||
[[Category: | [[Category: Cobalt]] | ||
[[Category: | [[Category: Disease mutation]] | ||
[[Category: | [[Category: Isomerase]] | ||
[[Category: | [[Category: Metabolic disease]] | ||
[[Category: | [[Category: Metal-binding]] | ||
[[Category: | [[Category: Methylmalonyl coa mutase deficiency]] | ||
[[Category: | [[Category: Mitochondrion]] | ||
[[Category: | [[Category: Organic aciduria]] | ||
[[Category: | [[Category: Polymorphism]] | ||
[[Category: | [[Category: Sgc]] | ||
[[Category: | [[Category: Structural genomic]] | ||
[[Category: | [[Category: Structural genomics consortium]] | ||
[[Category: | [[Category: Transit peptide]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 20:48:11 2008'' | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | |||
Revision as of 17:48, 4 May 2008
Crystal structure of human methylmalonyl-CoA mutase
Disease
Known disease associated with this structure: Methylmalonic aciduria, mut(0) type OMIM:[609058]
About this Structure
3BIC is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA. Page seeded by OCA on Sun May 4 20:48:11 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Methylmalonyl-CoA mutase
- Single protein
- 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
- Polymorphism
- Sgc
- Structural genomic
- Structural genomics consortium
- Transit peptide
