1sgh

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[[Image:1sgh.gif|left|200px]]
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{{Structure
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|GENE= MSN ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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{{STRUCTURE_1sgh| PDB=1sgh | SCENE= }}
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1sgh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1sgh OCA], [http://www.ebi.ac.uk/pdbsum/1sgh PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1sgh RCSB]</span>
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'''Moesin FERM domain bound to EBP50 C-terminal peptide'''
'''Moesin FERM domain bound to EBP50 C-terminal peptide'''
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[[Category: Ingraffea, J.]]
[[Category: Ingraffea, J.]]
[[Category: Karplus, P A.]]
[[Category: Karplus, P A.]]
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[[Category: ferm-peptide complex]]
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[[Category: Ferm-peptide complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 08:40:17 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:41:39 2008''
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Revision as of 05:40, 3 May 2008

Template:STRUCTURE 1sgh

Moesin FERM domain bound to EBP50 C-terminal peptide


Overview

Members of the ezrin-radixin-moesin (ERM) protein family serve as regulated microfilament-membrane crosslinking proteins that, upon activation, bind the scaffolding protein ERM-phosphoprotein of 50 kDa (EBP50). Here we report a 3.5 A resolution diffraction analysis of a complex between the active moesin N-terminal FERM domain and a 38 residue peptide from the C terminus of EBP50. This crystallographic result, combined with sequence and structural comparisons, suggests that the C-terminal 11 residues of EBP50 binds as an alpha-helix at the same site occupied in the dormant monomer by the last 11 residues of the inhibitory moesin C-terminal tail. Biochemical support for this interpretation derives from in vitro studies showing that appropriate mutations in both the EBP50 tail peptide and the FERM domain reduce binding, and that a peptide representing just the C-terminal 14 residues of EBP50 also binds to moesin. Combined with the recent identification of the I-CAM-2 binding site on the ERM FERM domain (Hamada, K., Shimizu, T., Yonemura, S., Tsukita, S., and Hakoshima, T. (2003) EMBO J. 22, 502-514), this study reveals that the FERM domain contains two distinct binding sites for membrane-associated proteins. The contribution of each ligand to ERM function can now be dissected by making structure-based mutations that specifically affect the binding of each ligand.

About this Structure

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

Reference

The EBP50-moesin interaction involves a binding site regulated by direct masking on the FERM domain., Finnerty CM, Chambers D, Ingraffea J, Faber HR, Karplus PA, Bretscher A, J Cell Sci. 2004 Mar 15;117(Pt 8):1547-52. PMID:15020681 Page seeded by OCA on Sat May 3 08:40:17 2008

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