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Structural genomics and drug discovery
Structure determination has already proven useful for lead optimization and direct drug design. The number of high-resolution structures available in public databases today exceeds 30,000 and will definitely aid in structure-based drug design. Structural genomics approaches covering whole genomes, t...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822824/ https://www.ncbi.nlm.nih.gov/pubmed/17488474 http://dx.doi.org/10.1111/j.1582-4934.2007.00028.x |
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author | Lundstrom, K |
author_facet | Lundstrom, K |
author_sort | Lundstrom, K |
collection | PubMed |
description | Structure determination has already proven useful for lead optimization and direct drug design. The number of high-resolution structures available in public databases today exceeds 30,000 and will definitely aid in structure-based drug design. Structural genomics approaches covering whole genomes, topologically similar proteins or gene families are great assets for further progress in the development of new drugs. However, membrane proteins representing 70% of current drug targets are poorly characterized structurally. The problems have been related to difficulties in obtaining large amount of recombinant membrane proteins as well as their purification and structure determination. Structural genomics has proven successful in developing new methods in areas from expression to structure determination by studying a large number of target proteins in parallel. |
format | Online Article Text |
id | pubmed-3822824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38228242015-04-27 Structural genomics and drug discovery Lundstrom, K J Cell Mol Med Reviews Structure determination has already proven useful for lead optimization and direct drug design. The number of high-resolution structures available in public databases today exceeds 30,000 and will definitely aid in structure-based drug design. Structural genomics approaches covering whole genomes, topologically similar proteins or gene families are great assets for further progress in the development of new drugs. However, membrane proteins representing 70% of current drug targets are poorly characterized structurally. The problems have been related to difficulties in obtaining large amount of recombinant membrane proteins as well as their purification and structure determination. Structural genomics has proven successful in developing new methods in areas from expression to structure determination by studying a large number of target proteins in parallel. Blackwell Publishing Ltd 2007-03 2007-05-01 /pmc/articles/PMC3822824/ /pubmed/17488474 http://dx.doi.org/10.1111/j.1582-4934.2007.00028.x Text en |
spellingShingle | Reviews Lundstrom, K Structural genomics and drug discovery |
title | Structural genomics and drug discovery |
title_full | Structural genomics and drug discovery |
title_fullStr | Structural genomics and drug discovery |
title_full_unstemmed | Structural genomics and drug discovery |
title_short | Structural genomics and drug discovery |
title_sort | structural genomics and drug discovery |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822824/ https://www.ncbi.nlm.nih.gov/pubmed/17488474 http://dx.doi.org/10.1111/j.1582-4934.2007.00028.x |
work_keys_str_mv | AT lundstromk structuralgenomicsanddrugdiscovery |