3SC0
Crystal Structure of MMACHC (1-238), a human B12 processing enzyme, complexed with MethylCobalamin
3SC0 の概要
| エントリーDOI | 10.2210/pdb3sc0/pdb |
| 関連するPDBエントリー | 3SBY 3SBZ |
| 分子名称 | Methylmalonic aciduria and homocystinuria type C protein, CO-METHYLCOBALAMIN (3 entities in total) |
| 機能のキーワード | mmachc, cblc, cobalamin, flavin, glutathione, flavin reductase, oxidoreductase, maturase |
| 由来する生物種 | Homo sapiens (human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 28833.89 |
| 構造登録者 | Koutmos, M.,Gherasim, C.,Smith, J.L.,Banerjee, R. (登録日: 2011-06-06, 公開日: 2011-06-22, 最終更新日: 2023-09-13) |
| 主引用文献 | Koutmos, M.,Gherasim, C.,Smith, J.L.,Banerjee, R. Structural basis of multifunctionality in a vitamin B12-processing enzyme. J.Biol.Chem., 286:29780-29787, 2011 Cited by PubMed Abstract: An early step in the intracellular processing of vitamin B(12) involves CblC, which exhibits dual reactivity, catalyzing the reductive decyanation of cyanocobalamin (vitamin B(12)), and the dealkylation of alkylcobalamins (e.g. methylcobalamin; MeCbl). Insights into how the CblC scaffold supports this chemical dichotomy have been unavailable despite it being the most common locus of patient mutations associated with inherited cobalamin disorders that manifest in both severe homocystinuria and methylmalonic aciduria. Herein, we report structures of human CblC, with and without bound MeCbl, which provide novel biochemical insights into its mechanism of action. Our results reveal that CblC is the most divergent member of the NADPH-dependent flavin reductase family and can use FMN or FAD as a prosthetic group to catalyze reductive decyanation. Furthermore, CblC is the first example of an enzyme with glutathione transferase activity that has a sequence and structure unrelated to the GST superfamily. CblC thus represents an example of evolutionary adaptation of a common structural platform to perform diverse chemistries. The CblC structure allows us to rationalize the biochemical basis of a number of pathological mutations associated with severe clinical phenotypes. PubMed: 21697092DOI: 10.1074/jbc.M111.261370 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.95 Å) |
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