3elj: Difference between revisions
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[[Image:3elj.png|left|200px]] | [[Image:3elj.png|left|200px]] | ||
{{STRUCTURE_3elj| PDB=3elj | SCENE= }} | {{STRUCTURE_3elj| PDB=3elj | SCENE= }} | ||
===Jnk1 complexed with a bis-anilino-pyrrolopyrimidine inhibitor.=== | ===Jnk1 complexed with a bis-anilino-pyrrolopyrimidine inhibitor.=== | ||
{{ABSTRACT_PUBMED_19071018}} | {{ABSTRACT_PUBMED_19071018}} | ||
==About this Structure== | ==About this Structure== | ||
[[3elj]] is a 1 chain structure of [[Mitogen-activated 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=3ELJ OCA]. | |||
==See Also== | |||
*[[Mitogen-activated protein kinase|Mitogen-activated protein kinase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:019071018</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Mitogen-activated protein kinase]] | [[Category: Mitogen-activated protein kinase]] | ||
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[[Category: Shewchuk, L.]] | [[Category: Shewchuk, L.]] | ||
[[Category: Vicentini, G.]] | [[Category: Vicentini, G.]] | ||
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: C-jun n-terminal kinase]] | [[Category: C-jun n-terminal kinase]] | ||
| Line 50: | Line 40: | ||
[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
[[Category: Serine/threonine-protein kinase]] | [[Category: Serine/threonine-protein kinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
Revision as of 05:22, 26 July 2012
Jnk1 complexed with a bis-anilino-pyrrolopyrimidine inhibitor.
Template:ABSTRACT PUBMED 19071018
About this Structure
3elj is a 1 chain structure of Mitogen-activated protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Chamberlain SD, Redman AM, Wilson JW, Deanda F, Shotwell JB, Gerding R, Lei H, Yang B, Stevens KL, Hassell AM, Shewchuk LM, Leesnitzer MA, Smith JL, Sabbatini P, Atkins C, Groy A, Rowand JL, Kumar R, Mook RA Jr, Moorthy G, Patnaik S. Optimization of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivity. Bioorg Med Chem Lett. 2009 Jan 15;19(2):360-4. Epub 2008 Nov 24. PMID:19071018 doi:S0960-894X(08)01461-3
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Mitogen-activated protein kinase
- Atkins, C.
- Chamberlain, S.
- Deanda, F.
- Dumble, M.
- Gerding, R.
- Groy, A.
- Korenchuk, S.
- Kumar, R.
- Lei, H.
- Mook, R.
- Moorthy, G.
- Mosley, J.
- Redman, A.
- Rowland, J.
- Shewchuk, L.
- Vicentini, G.
- Atp-binding
- C-jun n-terminal kinase
- Jnk1
- Kinase
- Nucleotide-binding
- Phosphoprotein
- Serine/threonine-protein kinase
- Transferase
