1tsm: Difference between revisions
No edit summary |
No edit summary |
||
Line 24: | Line 24: | ||
[[Category: structure-based drug design]] | [[Category: structure-based drug design]] | ||
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 16:05:42 2007'' |
Revision as of 17:00, 30 October 2007
|
L. CASEI THYMIDYLATE SYNTHASE WITH SPECIES SPECIFIC INHIBITOR
OverviewOverview
Thymidylate synthase is an attractive target for antiproliferative drug, design because of its key role in the synthesis of DNA. As such, the, enzyme has been widely targeted for anticancer applications. In principle, TS should also be a good target for drugs used to fight infectious, disease. In practice, TS is highly conserved across species, and it has, proven to be difficult to develop inhibitors that are selective for, microbial TS enzymes over the human enzyme. Using the structure of TS from, Lactobacillus casei in complex with the nonsubstrate analogue, phenolphthalein, inhibitors were designed to take advantage of features of, the bacterial enzyme that differ from those of the human enzyme. Upon, synthesis and testing, these inhibitors were found to be up to 40-fold, selective for ... [(full description)]
About this StructureAbout this Structure
1TSM is a [Single protein] structure of sequence from [Lactobacillus casei] with PO4 and MR2 as [ligands]. Active as [Thymidylate synthase], with EC number [2.1.1.45]. Structure known Active Site: CAT. Full crystallographic information is available from [OCA].
ReferenceReference
Structure-based design of inhibitors specific for bacterial thymidylate synthase., Stout TJ, Tondi D, Rinaldi M, Barlocco D, Pecorari P, Santi DV, Kuntz ID, Stroud RM, Shoichet BK, Costi MP, Biochemistry. 1999 Feb 2;38(5):1607-17. PMID:9931028
Page seeded by OCA on Tue Oct 30 16:05:42 2007