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Architecture of a fungal fatty acid synthase at 5 A resolution.
- Source :
-
Science (New York, N.Y.) [Science] 2006 Mar 03; Vol. 311 (5765), pp. 1263-7. - Publication Year :
- 2006
-
Abstract
- All steps of fatty acid synthesis in fungi are catalyzed by the fatty acid synthase, which forms a 2.6-megadalton alpha6beta6 complex. We have determined the molecular architecture of this multienzyme by fitting the structures of homologous enzymes that catalyze the individual steps of the reaction pathway into a 5 angstrom x-ray crystallographic electron density map. The huge assembly contains two separated reaction chambers, each equipped with three sets of active sites separated by distances up to approximately 130 angstroms, across which acyl carrier protein shuttles substrates during the reaction cycle. Regions of the electron density arising from well-defined structural features outside the catalytic domains separate the two reaction chambers and serve as a matrix in which domains carrying the various active sites are embedded. The structure rationalizes the compartmentalization of fatty acid synthesis, and the spatial arrangement of the active sites has specific implications for our understanding of the reaction cycle mechanism and of the architecture of multienzymes in general.
- Subjects :
- Acyl Carrier Protein chemistry
Acyl Carrier Protein metabolism
Binding Sites
Catalytic Domain
Crystallization
Crystallography, X-Ray
Dimerization
Fatty Acid Synthases isolation & purification
Fatty Acid Synthases metabolism
Fatty Acids biosynthesis
Models, Molecular
Protein Conformation
Protein Folding
Protein Structure, Quaternary
Protein Structure, Secondary
Protein Structure, Tertiary
Sequence Homology, Amino Acid
Ascomycota enzymology
Fatty Acid Synthases chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1095-9203
- Volume :
- 311
- Issue :
- 5765
- Database :
- MEDLINE
- Journal :
- Science (New York, N.Y.)
- Publication Type :
- Academic Journal
- Accession number :
- 16513976
- Full Text :
- https://doi.org/10.1126/science.1123251