3dcv: Difference between revisions

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{{Seed}}
{{Seed}}
[[Image:3dcv.jpg|left|200px]]
[[Image:3dcv.png|left|200px]]


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==About this Structure==
==About this Structure==
3DCV is a [[Single protein]] structure of 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=3DCV OCA].  
3DCV is a 1 chain structure of 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=3DCV OCA].  


==Reference==
==Reference==
4-(1H-indazol-5-yl)-6-phenylpyrimidin-2(1H)-one analogs as potent CDC7 inhibitors., Shafer CM, Lindvall M, Bellamacina C, Gesner TG, Yabannavar A, Jia W, Lin S, Walter A, Bioorg Med Chem Lett. 2008 Aug 15;18(16):4482-5. Epub 2008 Jul 17. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18672368 18672368]
<ref group="xtra">PMID:18672368</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Single protein]]
[[Category: Bellamacina, C R.]]
[[Category: Bellamacina, C R.]]
[[Category: Gesner, T G.]]
[[Category: Gesner, T G.]]
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[[Category: Transferase]]
[[Category: Transferase]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 20 12:16:02 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 11:51:11 2009''

Revision as of 09:51, 16 February 2009

File:3dcv.png

Template:STRUCTURE 3dcv

Crystal structure of human Pim1 kinase complexed with 4-(4-hydroxy-3-methyl-phenyl)-6-phenylpyrimidin-2(1H)-one

Template:ABSTRACT PUBMED 18672368

About this Structure

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

Reference

  1. Shafer CM, Lindvall M, Bellamacina C, Gesner TG, Yabannavar A, Jia W, Lin S, Walter A. 4-(1H-indazol-5-yl)-6-phenylpyrimidin-2(1H)-one analogs as potent CDC7 inhibitors. Bioorg Med Chem Lett. 2008 Aug 15;18(16):4482-5. Epub 2008 Jul 17. PMID:18672368 doi:10.1016/j.bmcl.2008.07.061

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