2cbl

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[[Image:2cbl.gif|left|200px]]
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{{Structure
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{{STRUCTURE_2cbl| PDB=2cbl | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2cbl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cbl OCA], [http://www.ebi.ac.uk/pdbsum/2cbl PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2cbl RCSB]</span>
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'''N-TERMINAL DOMAIN OF CBL IN COMPLEX WITH ITS BINDING SITE ON ZAP-70'''
'''N-TERMINAL DOMAIN OF CBL IN COMPLEX WITH ITS BINDING SITE ON ZAP-70'''
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[[Category: Meng, W.]]
[[Category: Meng, W.]]
[[Category: Sawasdikosol, S.]]
[[Category: Sawasdikosol, S.]]
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[[Category: complex (proto-oncogene/peptide)]]
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[[Category: Phosphotyrosine binding]]
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[[Category: phosphotyrosine binding]]
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[[Category: Proto-oncogene]]
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[[Category: proto-oncogene]]
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[[Category: Sh2]]
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[[Category: sh2]]
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[[Category: Signal transduction]]
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[[Category: signal transduction]]
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Revision as of 18:39, 3 May 2008

Template:STRUCTURE 2cbl

N-TERMINAL DOMAIN OF CBL IN COMPLEX WITH ITS BINDING SITE ON ZAP-70


Overview

Cbl is an adaptor protein that functions as a negative regulator of many signalling pathways that start from receptors at the cell surface. The evolutionarily conserved amino-terminal region of Cbl (Cbl-N) binds to phosphorylated tyrosine residues and has cell-transforming activity. Point mutations in Cbl that disrupt its recognition of phosphotyrosine also interfere with its negative regulatory function and, in the case of v-cbl, with its oncogenic potential. In T cells, Cbl-N binds to the tyrosine-phosphorylated inhibitory site of the protein tyrosine kinase ZAP-70. Here we describe the crystal structure of Cbl-N, both alone and in complex with a phosphopeptide that represents its binding site in ZAP-70. The structures show that Cbl-N is composed of three interacting domains: a four-helix bundle (4H), an EF-hand calcium-binding domain, and a divergent SH2 domain that was not recognizable from the amino-acid sequence of the protein. The calcium-bound EF hand wedges between the 4H and SH2 domains and roughly determines their relative orientation. In the ligand-occupied structure, the 4H domain packs against the SH2 domain and completes its phosphotyrosine-recognition pocket. Disruption of this binding to ZAP-70 as a result of structure-based mutations in the 4H, EF-hand and SH2 domains confirms that the three domains together form an integrated phosphoprotein-recognition module.

About this Structure

2CBL is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structure of the amino-terminal domain of Cbl complexed to its binding site on ZAP-70 kinase., Meng W, Sawasdikosol S, Burakoff SJ, Eck MJ, Nature. 1999 Mar 4;398(6722):84-90. PMID:10078535 Page seeded by OCA on Sat May 3 21:39:25 2008

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