1o4e
From Proteopedia
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[[Image:1o4e.png|left|200px]] | [[Image:1o4e.png|left|200px]] | ||
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{{STRUCTURE_1o4e| PDB=1o4e | SCENE= }} | {{STRUCTURE_1o4e| PDB=1o4e | SCENE= }} | ||
===CRYSTAL STRUCTURE OF SH2 IN COMPLEX WITH RU78299.=== | ===CRYSTAL STRUCTURE OF SH2 IN COMPLEX WITH RU78299.=== | ||
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{{ABSTRACT_PUBMED_14613321}} | {{ABSTRACT_PUBMED_14613321}} | ||
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| - | ==Disease== | ||
| - | Known disease associated with this structure: Colon cancer, advanced OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190090 190090]] | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1o4e]] is a 1 chain structure of [[Proto-oncogene tyrosine-protein kinase]] 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=1O4E OCA]. | |
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| + | ==See Also== | ||
| + | *[[Proto-oncogene tyrosine-protein kinase|Proto-oncogene tyrosine-protein kinase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:014613321</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
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[[Category: Loenze, P.]] | [[Category: Loenze, P.]] | ||
[[Category: Sh2 domain fragment approach]] | [[Category: Sh2 domain fragment approach]] | ||
| - | + | [[Category: Signaling protein]] | |
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Revision as of 07:41, 27 July 2012
Contents |
CRYSTAL STRUCTURE OF SH2 IN COMPLEX WITH RU78299.
Template:ABSTRACT PUBMED 14613321
About this Structure
1o4e is a 1 chain structure of Proto-oncogene tyrosine-protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Lange G, Lesuisse D, Deprez P, Schoot B, Loenze P, Benard D, Marquette JP, Broto P, Sarubbi E, Mandine E. Requirements for specific binding of low affinity inhibitor fragments to the SH2 domain of (pp60)Src are identical to those for high affinity binding of full length inhibitors. J Med Chem. 2003 Nov 20;46(24):5184-95. PMID:14613321 doi:http://dx.doi.org/10.1021/jm020970s
