2b1p: Difference between revisions
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[[Image:2b1p. | {{Seed}} | ||
[[Image:2b1p.png|left|200px]] | |||
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{{STRUCTURE_2b1p| PDB=2b1p | SCENE= }} | {{STRUCTURE_2b1p| PDB=2b1p | SCENE= }} | ||
===inhibitor complex of JNK3=== | |||
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The | The line below this paragraph, {{ABSTRACT_PUBMED_16140012}}, adds the Publication Abstract to the page | ||
(as it appears on PubMed at http://www.pubmed.gov), where 16140012 is the PubMed ID number. | |||
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{{ABSTRACT_PUBMED_16140012}} | |||
==About this Structure== | ==About this Structure== | ||
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[[Category: Enzyme-inhibitor complex]] | [[Category: Enzyme-inhibitor complex]] | ||
[[Category: Kinase inhibitor]] | [[Category: Kinase inhibitor]] | ||
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 22:36:11 2008'' | |||
Revision as of 19:36, 27 July 2008
inhibitor complex of JNK3
Template:ABSTRACT PUBMED 16140012
About this Structure
2B1P is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3., Swahn BM, Huerta F, Kallin E, Malmstrom J, Weigelt T, Viklund J, Womack P, Xue Y, Ohberg L, Bioorg Med Chem Lett. 2005 Nov 15;15(22):5095-9. PMID:16140012
Page seeded by OCA on Sun Jul 27 22:36:11 2008
