1u2b
From Proteopedia
(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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| - | [[Image:1u2b.gif|left|200px]]<br /><applet load="1u2b" size=" | + | [[Image:1u2b.gif|left|200px]]<br /><applet load="1u2b" size="350" color="white" frame="true" align="right" spinBox="true" |
caption="1u2b, resolution 1.80Å" /> | caption="1u2b, resolution 1.80Å" /> | ||
'''Triglycine variant of the Grp1 Pleckstrin Homology Domain unliganded'''<br /> | '''Triglycine variant of the Grp1 Pleckstrin Homology Domain unliganded'''<br /> | ||
==Overview== | ==Overview== | ||
| - | The pleckstrin homology (PH) domains of the homologous proteins Grp1 | + | 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== | ==About this Structure== | ||
| - | 1U2B is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with SO4 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http:// | + | 1U2B is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U2B OCA]. |
==Reference== | ==Reference== | ||
| Line 13: | Line 13: | ||
[[Category: Mus musculus]] | [[Category: Mus musculus]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
| - | [[Category: Cronin, T | + | [[Category: Cronin, T C.]] |
| - | [[Category: Czech, M | + | [[Category: Czech, M P.]] |
| - | [[Category: DiNitto, J | + | [[Category: DiNitto, J P.]] |
| - | [[Category: Lambright, D | + | [[Category: Lambright, D G.]] |
[[Category: SO4]] | [[Category: SO4]] | ||
[[Category: lipid binding]] | [[Category: lipid binding]] | ||
| Line 22: | Line 22: | ||
[[Category: phosphoinositides]] | [[Category: phosphoinositides]] | ||
| - | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:19:58 2008'' |
Revision as of 13:20, 21 February 2008
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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 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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