3odk

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3odk.jpg|left|200px]]
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The entry 3odk is ON HOLD until Paper Publication
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{{STRUCTURE_3odk| PDB=3odk | SCENE= }}
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Authors: Potter, A., Oldfield, V., Nunns, C., Fromont, C., Ray, S., Northfield, C.J., Bryant, C.J., Scrace, S.F., Robinson, D., Matossova, N., Baker, L., Dokurno, P., Surgenor, A.E., Davis, B.E., Richardson, C.M., Murray, J.B., Moore, J.D.
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===Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution===
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Description: Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 25 08:38:25 2010''
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(as it appears on PubMed at http://www.pubmed.gov), where 20932746 is the PubMed ID number.
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{{ABSTRACT_PUBMED_20932746}}
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==About this Structure==
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3ODK is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3ODK OCA].
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==Reference==
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<ref group="xtra">PMID:20932746</ref><references group="xtra"/>
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[[Category: Homo sapiens]]
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[[Category: Peptidylprolyl isomerase]]
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[[Category: Baker, L.]]
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[[Category: Bryant, C J.]]
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[[Category: Davis, B E.]]
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[[Category: Dokurno, P.]]
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[[Category: Fromont, C.]]
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[[Category: Matossova, N.]]
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[[Category: Moore, J D.]]
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[[Category: Murray, J B.]]
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[[Category: Northfield, C J.]]
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[[Category: Nunns, C.]]
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[[Category: Oldfield, V.]]
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[[Category: Potter, A.]]
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[[Category: Ray, S.]]
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[[Category: Richardson, C M.]]
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[[Category: Robinson, D.]]
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[[Category: Scrace, S F.]]
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[[Category: Surgenor, A E.]]
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[[Category: Cell cycle]]
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[[Category: Isomerase]]
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[[Category: Nucleus]]
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[[Category: Oncogenic transformation]]
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[[Category: Phosphoprotein]]
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[[Category: Ppiase]]
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[[Category: Proline directed kinase]]
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[[Category: Rotamase]]
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[[Category: Sbdd]]
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[[Category: Small molecule]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 27 12:14:07 2010''

Revision as of 09:03, 27 October 2010

Image:3odk.jpg

Template:STRUCTURE 3odk

Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution

Template:ABSTRACT PUBMED 20932746

About this Structure

3ODK is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Potter A, Oldfield V, Nunns C, Fromont C, Ray S, Northfield CJ, Bryant CJ, Scrace SF, Robinson D, Matossova N, Baker L, Dokurno P, Surgenor AE, Davis B, Richardson CM, Murray JB, Moore JD. Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6483-8. Epub 2010 Sep 17. PMID:20932746 doi:10.1016/j.bmcl.2010.09.063

Page seeded by OCA on Wed Oct 27 12:14:07 2010

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