Abstract
The initial aim of the Berkeley Structural Genomics Center is to obtain a near-complete structural complement of two minimal organisms, closely related pathogens Mycoplasma genitalium and M. pneumoniae. The former has fewer than 500 genes and the latter fewer than 700 genes. To achieve this goal, the current protein targets have been selected starting with those predicted to be most tractable and likely to yield new structural and functional information. During the past 3 years, the semi-automated structural genomics pipeline has been set up from cloning, expression, purification, and ultimately to structural determination. The results from the pipeline substantially increased the coverage of the protein fold space of M. pneumoniae and M. genitalium. Furthermore, about 1/2 of the structures of 'unique' protein sequences revealed new and novel folds, and over 2/3 of the structures of previously annotated 'hypothetical proteins' inferred their molecular functions.
Original language | English |
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Pages (from-to) | 63-70 |
Number of pages | 8 |
Journal | Journal of Structural and Functional Genomics |
Volume | 6 |
Issue number | 2-3 |
DOIs | |
State | Published - Sep 2005 |
Bibliographical note
Funding Information:We thank all the component members of BSGC for their efforts towards accomplishing the BSGC objectives. We gratefully acknowledge the support of NIH grant GM62412 for the structures cited in this article.
Keywords
- Berkeley Structural Genomics Center
- Minimal organisms
- Molecular function
- Protein fold space
- Structural genomics