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The Center for Eukaryotic Structural Genomics
The Center for Eukaryotic Structural Genomics (CESG) is a “specialized” or “technology development” center supported by the Protein Structure Initiative (PSI). CESG’s mission is to develop improved methods for the high-throughput solution of structures from eukaryotic proteins, with a very strong we...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705709/ https://www.ncbi.nlm.nih.gov/pubmed/19130299 http://dx.doi.org/10.1007/s10969-008-9057-4 |
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author | Markley, John L. Aceti, David J. Bingman, Craig A. Fox, Brian G. Frederick, Ronnie O. Makino, Shin-ichi Nichols, Karl W. Phillips, George N. Primm, John G. Sahu, Sarata C. Vojtik, Frank C. Volkman, Brian F. Wrobel, Russell L. Zolnai, Zsolt |
author_facet | Markley, John L. Aceti, David J. Bingman, Craig A. Fox, Brian G. Frederick, Ronnie O. Makino, Shin-ichi Nichols, Karl W. Phillips, George N. Primm, John G. Sahu, Sarata C. Vojtik, Frank C. Volkman, Brian F. Wrobel, Russell L. Zolnai, Zsolt |
author_sort | Markley, John L. |
collection | PubMed |
description | The Center for Eukaryotic Structural Genomics (CESG) is a “specialized” or “technology development” center supported by the Protein Structure Initiative (PSI). CESG’s mission is to develop improved methods for the high-throughput solution of structures from eukaryotic proteins, with a very strong weighting toward human proteins of biomedical relevance. During the first three years of PSI-2, CESG selected targets representing 601 proteins from Homo sapiens, 33 from mouse, 10 from rat, 139 from Galdieria sulphuraria, 35 from Arabidopsis thaliana, 96 from Cyanidioschyzon merolae, 80 from Plasmodium falciparum, 24 from yeast, and about 25 from other eukaryotes. Notably, 30% of all structures of human proteins solved by the PSI Centers were determined at CESG. Whereas eukaryotic proteins generally are considered to be much more challenging targets than prokaryotic proteins, the technology now in place at CESG yields success rates that are comparable to those of the large production centers that work primarily on prokaryotic proteins. We describe here the technological innovations that underlie CESG’s platforms for bioinformatics and laboratory information management, target selection, protein production, and structure determination by X-ray crystallography or NMR spectroscopy. |
format | Text |
id | pubmed-2705709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-27057092009-07-07 The Center for Eukaryotic Structural Genomics Markley, John L. Aceti, David J. Bingman, Craig A. Fox, Brian G. Frederick, Ronnie O. Makino, Shin-ichi Nichols, Karl W. Phillips, George N. Primm, John G. Sahu, Sarata C. Vojtik, Frank C. Volkman, Brian F. Wrobel, Russell L. Zolnai, Zsolt J Struct Funct Genomics Article The Center for Eukaryotic Structural Genomics (CESG) is a “specialized” or “technology development” center supported by the Protein Structure Initiative (PSI). CESG’s mission is to develop improved methods for the high-throughput solution of structures from eukaryotic proteins, with a very strong weighting toward human proteins of biomedical relevance. During the first three years of PSI-2, CESG selected targets representing 601 proteins from Homo sapiens, 33 from mouse, 10 from rat, 139 from Galdieria sulphuraria, 35 from Arabidopsis thaliana, 96 from Cyanidioschyzon merolae, 80 from Plasmodium falciparum, 24 from yeast, and about 25 from other eukaryotes. Notably, 30% of all structures of human proteins solved by the PSI Centers were determined at CESG. Whereas eukaryotic proteins generally are considered to be much more challenging targets than prokaryotic proteins, the technology now in place at CESG yields success rates that are comparable to those of the large production centers that work primarily on prokaryotic proteins. We describe here the technological innovations that underlie CESG’s platforms for bioinformatics and laboratory information management, target selection, protein production, and structure determination by X-ray crystallography or NMR spectroscopy. Springer Netherlands 2009-01-08 2009-04 /pmc/articles/PMC2705709/ /pubmed/19130299 http://dx.doi.org/10.1007/s10969-008-9057-4 Text en © The Author(s) 2009 |
spellingShingle | Article Markley, John L. Aceti, David J. Bingman, Craig A. Fox, Brian G. Frederick, Ronnie O. Makino, Shin-ichi Nichols, Karl W. Phillips, George N. Primm, John G. Sahu, Sarata C. Vojtik, Frank C. Volkman, Brian F. Wrobel, Russell L. Zolnai, Zsolt The Center for Eukaryotic Structural Genomics |
title | The Center for Eukaryotic Structural Genomics |
title_full | The Center for Eukaryotic Structural Genomics |
title_fullStr | The Center for Eukaryotic Structural Genomics |
title_full_unstemmed | The Center for Eukaryotic Structural Genomics |
title_short | The Center for Eukaryotic Structural Genomics |
title_sort | center for eukaryotic structural genomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705709/ https://www.ncbi.nlm.nih.gov/pubmed/19130299 http://dx.doi.org/10.1007/s10969-008-9057-4 |
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