2f82

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|ACTIVITY=
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|RELATEDENTRY=[[2f9a|2F9A]], [[2fa3|2FA3]], [[2fa0|2FA0]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2f82 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2f82 OCA], [http://www.ebi.ac.uk/pdbsum/2f82 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2f82 RCSB]</span>
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[[Category: hmgs1]]
[[Category: hmgs1]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:59:10 2008''

Revision as of 23:59, 30 March 2008


PDB ID 2f82

Drag the structure with the mouse to rotate
, resolution 2.10Å
Related: 2F9A, 2FA3, 2FA0


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



HMG-CoA synthase from Brassica juncea in the apo-form


Overview

3-Hydroxy-3-methylglutaryl CoA synthase (HMGS) catalyzes the first committed step in the mevalonate metabolic pathway for isoprenoid biosynthesis and serves as an alternative target for cholesterol-lowering and antibiotic drugs. We have determined a previously undescribed crystal structure of a eukaryotic HMGS bound covalently to a potent and specific inhibitor F-244 [(E,E)-11-[3-(hydroxymethyl)-4-oxo-2-oxytanyl]-3,5,7-trimethyl-2,4-undecad ienenoic acid]. Given the accessibility of synthetic analogs of the F-244 natural product, this inhibited eukaryotic HMGS structure serves as a necessary starting point for structure-based methods that may improve the potency and species-specific selectivity of the next generation of F-244 analogs designed to target particular eukaryotic and prokaryotic HMGS.

About this Structure

2F82 is a Single protein structure of sequence from Brassica juncea. Full crystallographic information is available from OCA.

Reference

Structural basis for the design of potent and species-specific inhibitors of 3-hydroxy-3-methylglutaryl CoA synthases., Pojer F, Ferrer JL, Richard SB, Nagegowda DA, Chye ML, Bach TJ, Noel JP, Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11491-6. Epub 2006 Jul 24. PMID:16864776

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