An unanticipated architecture of the 750-kDa α6β6 holoenzyme of 3-methylcrotonyl-CoA carboxylase
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/nature10691.pdf
Reference33 articles.
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3. Holzinger, A. et al. Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA carboxylase deficiency. Hum. Mol. Genet. 10, 1299–1306 (2001)
4. Desviat, L. R. et al. Functional analysis of MCCA and MCCB mutations causing methylcrotonylglycinuria. Mol. Genet. Metab. 80, 315–320 (2003)
5. Wakil, S. J., Stoops, J. K. & Joshi, V. C. Fatty acid synthesis and its regulation. Annu. Rev. Biochem. 52, 537–579 (1983)
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