3hmm: Difference between revisions

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


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{{STRUCTURE_3hmm|  PDB=3hmm  |  SCENE=  }}  
{{STRUCTURE_3hmm|  PDB=3hmm  |  SCENE=  }}  


===Structure of Alk5 + GW855857===
===Structure of Alk5 + GW855857===


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{{ABSTRACT_PUBMED_19285388}}
{{ABSTRACT_PUBMED_19285388}}


==About this Structure==
==About this Structure==
3HMM is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=3gxj 3gxj]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3HMM OCA].  
[[3hmm]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=3gxj 3gxj]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3HMM OCA].  


==Reference==
==Reference==
<ref group="xtra">PMID:19285388</ref><references group="xtra"/>
<ref group="xtra">PMID:019285388</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Receptor protein serine/threonine kinase]]
[[Category: Receptor protein serine/threonine kinase]]
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[[Category: Transferase]]
[[Category: Transferase]]
[[Category: Transmembrane]]
[[Category: Transmembrane]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Jun 25 08:20:07 2009''

Revision as of 14:52, 6 March 2013

File:3hmm.png

Template:STRUCTURE 3hmm

Structure of Alk5 + GW855857

Template:ABSTRACT PUBMED 19285388

About this Structure

3hmm is a 1 chain structure with sequence from Homo sapiens. This structure supersedes the now removed PDB entry 3gxj. Full crystallographic information is available from OCA.

Reference

  1. Gellibert F, Fouchet MH, Nguyen VL, Wang R, Krysa G, de Gouville AC, Huet S, Dodic N. Design of novel quinazoline derivatives and related analogues as potent and selective ALK5 inhibitors. Bioorg Med Chem Lett. 2009 Apr 15;19(8):2277-81. Epub 2009 Feb 26. PMID:19285388 doi:10.1016/j.bmcl.2009.02.087

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