2uwd
From Proteopedia
(Difference between revisions)
m (Protected "2uwd" [edit=sysop:move=sysop]) |
|||
| Line 1: | Line 1: | ||
[[Image:2uwd.png|left|200px]] | [[Image:2uwd.png|left|200px]] | ||
| - | <!-- | ||
| - | The line below this paragraph, containing "STRUCTURE_2uwd", creates the "Structure Box" on the page. | ||
| - | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
| - | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
| - | or leave the SCENE parameter empty for the default display. | ||
| - | --> | ||
{{STRUCTURE_2uwd| PDB=2uwd | SCENE= }} | {{STRUCTURE_2uwd| PDB=2uwd | SCENE= }} | ||
===INHIBITION OF THE HSP90 MOLECULAR CHAPERONE IN VITRO AND IN VIVO BY NOVEL, SYNTHETIC, POTENT RESORCINYLIC PYRAZOLE, ISOXAZOLE AMIDE ANALOGS=== | ===INHIBITION OF THE HSP90 MOLECULAR CHAPERONE IN VITRO AND IN VIVO BY NOVEL, SYNTHETIC, POTENT RESORCINYLIC PYRAZOLE, ISOXAZOLE AMIDE ANALOGS=== | ||
| - | |||
| - | <!-- | ||
| - | The line below this paragraph, {{ABSTRACT_PUBMED_17431102}}, adds the Publication Abstract to the page | ||
| - | (as it appears on PubMed at http://www.pubmed.gov), where 17431102 is the PubMed ID number. | ||
| - | --> | ||
{{ABSTRACT_PUBMED_17431102}} | {{ABSTRACT_PUBMED_17431102}} | ||
| Line 22: | Line 11: | ||
==See Also== | ==See Also== | ||
| - | *[[Heat Shock Proteins]] | + | *[[Heat Shock Proteins|Heat Shock Proteins]] |
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:017431102</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Aherne, W.]] | [[Category: Aherne, W.]] | ||
Revision as of 03:53, 27 July 2012
Contents |
INHIBITION OF THE HSP90 MOLECULAR CHAPERONE IN VITRO AND IN VIVO BY NOVEL, SYNTHETIC, POTENT RESORCINYLIC PYRAZOLE, ISOXAZOLE AMIDE ANALOGS
Template:ABSTRACT PUBMED 17431102
About this Structure
2uwd is a 1 chain structure of Heat Shock Proteins with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Sharp SY, Prodromou C, Boxall K, Powers MV, Holmes JL, Box G, Matthews TP, Cheung KM, Kalusa A, James K, Hayes A, Hardcastle A, Dymock B, Brough PA, Barril X, Cansfield JE, Wright L, Surgenor A, Foloppe N, Hubbard RE, Aherne W, Pearl L, Jones K, McDonald E, Raynaud F, Eccles S, Drysdale M, Workman P. Inhibition of the heat shock protein 90 molecular chaperone in vitro and in vivo by novel, synthetic, potent resorcinylic pyrazole/isoxazole amide analogues. Mol Cancer Ther. 2007 Apr;6(4):1198-211. PMID:17431102 doi:6/4/1198
Categories: Homo sapiens | Aherne, W. | Barril, X. | Box, G. | Boxall, K. | Brough, P A. | Cansfield, J E. | Cheung, K M. | Drysdale, M. | Dymock, B. | Eccles, S. | Foloppe, N. | Hardcastle, A. | Hayes, A. | Holmes, J L. | James, K. | Jones, K. | Kalusa, A. | Matthews, T P. | Mcdonald, E. | Pearl, L. | Powers, M V. | Prodromou, C. | Raynaud, F. | Sharp, S Y. | Surgenor, A. | Workman, P. | Wright, L M. | Atp-binding | Chaperone | Heat shock | Nucleotide-binding | Phosphorylation
