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2p0c

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{{Seed}}
 
[[Image:2p0c.png|left|200px]]
[[Image:2p0c.png|left|200px]]
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==About this Structure==
==About this Structure==
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2P0C is a 2 chains structure with sequences 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=2P0C OCA].
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[[2p0c]] is a 2 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=2P0C OCA].
==Reference==
==Reference==
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[[Category: Dhe-Paganon, S.]]
[[Category: Dhe-Paganon, S.]]
[[Category: Edwards, A M.]]
[[Category: Edwards, A M.]]
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[[Category: Finerty, P J.]]
[[Category: Huang, X.]]
[[Category: Huang, X.]]
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[[Category: Jr., P J.Finerty.]]
 
[[Category: SGC, Structural Genomics Consortium.]]
[[Category: SGC, Structural Genomics Consortium.]]
[[Category: Sundstrom, M.]]
[[Category: Sundstrom, M.]]
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[[Category: Tyrosine-protein kinase]]
[[Category: Tyrosine-protein kinase]]
[[Category: Vision]]
[[Category: Vision]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu May 20 09:03:24 2010''
 

Revision as of 21:52, 14 March 2011

Template:STRUCTURE 2p0c

Catalytic Domain of the Proto-oncogene Tyrosine-protein Kinase MER

Template:ABSTRACT PUBMED 19028587

About this Structure

2p0c is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Huang X, Finerty P Jr, Walker JR, Butler-Cole C, Vedadi M, Schapira M, Parker SA, Turk BE, Thompson DA, Dhe-Paganon S. Structural insights into the inhibited states of the Mer receptor tyrosine kinase. J Struct Biol. 2009 Feb;165(2):88-96. Epub 2008 Nov 5. PMID:19028587 doi:10.1016/j.jsb.2008.10.003
  • Graham DK, Dawson TL, Mullaney DL, Snodgrass HR, Earp HS. Cloning and mRNA expression analysis of a novel human protooncogene, c-mer. Cell Growth Differ. 1994 Jun;5(6):647-57. PMID:8086340
  • Gal A, Li Y, Thompson DA, Weir J, Orth U, Jacobson SG, Apfelstedt-Sylla E, Vollrath D. Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa. Nat Genet. 2000 Nov;26(3):270-1. PMID:11062461 doi:10.1038/81555

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