1ump
From Proteopedia
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[[Image:1ump.png|left|200px]] | [[Image:1ump.png|left|200px]] | ||
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{{STRUCTURE_1ump| PDB=1ump | SCENE= }} | {{STRUCTURE_1ump| PDB=1ump | SCENE= }} | ||
===GEOMETRY OF TRITERPENE CONVERSION TO PENTACARBOCYCLIC HOPENE=== | ===GEOMETRY OF TRITERPENE CONVERSION TO PENTACARBOCYCLIC HOPENE=== | ||
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{{ABSTRACT_PUBMED_15113001}} | {{ABSTRACT_PUBMED_15113001}} | ||
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==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:015113001</ref><ref group="xtra">PMID:012031670</ref><ref group="xtra">PMID:009931258</ref><ref group="xtra">PMID:009070455</ref><references group="xtra"/> |
[[Category: Alicyclobacillus acidocaldarius]] | [[Category: Alicyclobacillus acidocaldarius]] | ||
[[Category: Oxidosqualene Cyclase]] | [[Category: Oxidosqualene Cyclase]] |
Revision as of 09:25, 16 January 2013
GEOMETRY OF TRITERPENE CONVERSION TO PENTACARBOCYCLIC HOPENE
Template:ABSTRACT PUBMED 15113001
About this Structure
1ump is a 3 chain structure with sequence from Alicyclobacillus acidocaldarius. The December 2007 RCSB PDB Molecule of the Month feature on Oxidosqualene Cyclase by David S. Goodsell is 10.2210/rcsb_pdb/mom_2007_12. Full crystallographic information is available from OCA.
Reference
- Reinert DJ, Balliano G, Schulz GE. Conversion of squalene to the pentacarbocyclic hopene. Chem Biol. 2004 Jan;11(1):121-6. PMID:15113001 doi:http://dx.doi.org/10.1016/j.chembiol.2003.12.013
- Lenhart A, Weihofen WA, Pleschke AE, Schulz GE. Crystal structure of a squalene cyclase in complex with the potential anticholesteremic drug Ro48-8071. Chem Biol. 2002 May;9(5):639-45. PMID:12031670
- Wendt KU, Lenhart A, Schulz GE. The structure of the membrane protein squalene-hopene cyclase at 2.0 A resolution. J Mol Biol. 1999 Feb 12;286(1):175-87. PMID:9931258 doi:http://dx.doi.org/10.1006/jmbi.1998.2470
- Wendt KU, Feil C, Lenhart A, Poralla K, Schulz GE. Crystallization and preliminary X-ray crystallographic analysis of squalene-hopene cyclase from Alicyclobacillus acidocaldarius. Protein Sci. 1997 Mar;6(3):722-4. PMID:9070455 doi:10.1002/pro.5560060322