1ukh: Difference between revisions

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[[Image:1ukh.jpg|left|200px]]
[[Image:1ukh.jpg|left|200px]]


{{Structure
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Non-specific_serine/threonine_protein_kinase Non-specific serine/threonine protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.1 2.7.11.1] </span>
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|RELATEDENTRY=[[1uki|1UKI]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ukh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ukh OCA], [http://www.ebi.ac.uk/pdbsum/1ukh PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1ukh RCSB]</span>
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'''Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125'''
'''Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125'''
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[[Category: Sung, B J.]]
[[Category: Sung, B J.]]
[[Category: Yang, C H.]]
[[Category: Yang, C H.]]
[[Category: phosphorylation]]
[[Category: Phosphorylation]]
[[Category: transferase]]
[[Category: Transferase]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 11:21:10 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:11:31 2008''

Revision as of 11:21, 3 May 2008

File:1ukh.jpg

Template:STRUCTURE 1ukh

Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125


OverviewOverview

The c-jun N-terminal kinase (JNK) signaling pathway is regulated by JNK-interacting protein-1 (JIP1), which is a scaffolding protein assembling the components of the JNK cascade. Overexpression of JIP1 deactivates the JNK pathway selectively by cytoplasmic retention of JNK and thereby inhibits gene expression mediated by JNK, which occurs in the nucleus. Here, we report the crystal structure of human JNK1 complexed with pepJIP1, the peptide fragment of JIP1, revealing its selectivity for JNK1 over other MAPKs and the allosteric inhibition mechanism. The van der Waals contacts by the three residues (Pro157, Leu160, and Leu162) of pepJIP1 and the hydrogen bonding between Glu329 of JNK1 and Arg156 of pepJIP1 are critical for the selective binding. Binding of the peptide also induces a hinge motion between the N- and C-terminal domains of JNK1 and distorts the ATP-binding cleft, reducing the affinity of the kinase for ATP. In addition, we also determined the ternary complex structure of pepJIP1-bound JNK1 complexed with SP600125, an ATP-competitive inhibitor of JNK, providing the basis for the JNK specificity of the compound.

About this StructureAbout this Structure

1UKH is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125., Heo YS, Kim SK, Seo CI, Kim YK, Sung BJ, Lee HS, Lee JI, Park SY, Kim JH, Hwang KY, Hyun YL, Jeon YH, Ro S, Cho JM, Lee TG, Yang CH, EMBO J. 2004 Jun 2;23(11):2185-95. Epub 2004 May 13. PMID:15141161 Page seeded by OCA on Sat May 3 11:21:10 2008

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