1u2b
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(New page: 200px<br /><applet load="1u2b" size="450" color="white" frame="true" align="right" spinBox="true" caption="1u2b, resolution 1.80Å" /> '''Triglycine variant o...)
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Revision as of 01:40, 21 November 2007
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Triglycine variant of the Grp1 Pleckstrin Homology Domain unliganded
Overview
The pleckstrin homology (PH) domains of the homologous proteins Grp1, (general receptor for phosphoinositides), ARNO (Arf nucleotide binding, site opener), and Cytohesin-1 bind phosphatidylinositol (PtdIns), 3,4,5-trisphosphate with unusually high selectivity. Remarkably, splice, variants that differ only by the insertion of a single glycine residue in, the beta1/beta2 loop exhibit dual specificity for PtdIns(3,4,5)P(3) and, PtdIns(4,5)P(2). The structural basis for this dramatic specificity switch, is not apparent from the known modes of phosphoinositide recognition., Here, we report crystal structures for dual specificity variants of the, Grp1 and ARNO PH domains in either the unliganded form or in complex with, the head groups of PtdIns(4,5)P(2) and PtdIns(3,4,5)P(3). Loss of contacts, with the beta1/beta2 loop with no significant change in head group, orientation accounts for the significant decrease in PtdIns(3,4,5)P(3), affinity observed for the dual specificity variants. Conversely, a small, increase rather than decrease in affinity for PtdIns(4,5)P(2) is explained, by a novel binding mode, in which the glycine insertion alleviates, unfavorable interactions with the beta1/beta2 loop. These observations are, supported by a systematic mutational analysis of the determinants of, phosphoinositide recognition.
About this Structure
1U2B is a Single protein structure of sequence from Mus musculus with SO4 as ligand. Full crystallographic information is available from OCA.
Reference
Structural determinants of phosphoinositide selectivity in splice variants of Grp1 family PH domains., Cronin TC, DiNitto JP, Czech MP, Lambright DG, EMBO J. 2004 Oct 1;23(19):3711-20. Epub 2004 Sep 9. PMID:15359279
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