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(New page: 200px<br /> <applet load="1pic" size="450" color="white" frame="true" align="right" spinBox="true" caption="1pic" /> '''PHOSPHATIDYLINOSITOL 3-KINASE, P85-ALPHA SU...)
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'''PHOSPHATIDYLINOSITOL 3-KINASE, P85-ALPHA SUBUNIT: C-TERMINAL SH2 DOMAIN COMPLEXED WITH A TYR751 PHOSPHOPEPTIDE FROM THE PDGF RECEPTOR, NMR, MINIMIZED MEAN STRUCTURE'''<br />
'''PHOSPHATIDYLINOSITOL 3-KINASE, P85-ALPHA SUBUNIT: C-TERMINAL SH2 DOMAIN COMPLEXED WITH A TYR751 PHOSPHOPEPTIDE FROM THE PDGF RECEPTOR, NMR, MINIMIZED MEAN STRUCTURE'''<br />
==Overview==
==Overview==
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We have determined the solution structure of the C-terminal SH2 domain of, the p85 alpha subunit of human phosphatidylinositol (PI) 3-kinase (EC, 2.7.1.137) in complex with a phosphorylated tyrosine pentapeptide sequence, from the platelet-derived growth factor receptor using heteronuclear, nuclear magnetic resonance spectroscopy. Overall, the structure is similar, to other SH2 domain complexes, but displays different detail interactions, within the phosphotyrosine binding site and in the recognition site for, the +3 methionine residue of the peptide, the side chain of which inserts, into a particularly deep and narrow pocket which is displaced relative to, that of other SH2 domains. The contacts made within this +3 pocket provide, the structural basis for the strong selection for methionine at this, position which characterizes the SH2 domains of PI3-kinase. Comparison, with spectral and structural features of the uncomplexed domain shows that, the long BG loop becomes less mobile in the presence of the bound peptide., In contrast, extreme resonance broadening encountered for most residues in, the beta D', beta E and beta F strands and associated connecting loops of, the domain in the absence of peptide persists in the complex, implying, conformational averaging in this part of the molecule on a, microsecond-to-millisecond time scale.
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We have determined the solution structure of the C-terminal SH2 domain of the p85 alpha subunit of human phosphatidylinositol (PI) 3-kinase (EC 2.7.1.137) in complex with a phosphorylated tyrosine pentapeptide sequence from the platelet-derived growth factor receptor using heteronuclear nuclear magnetic resonance spectroscopy. Overall, the structure is similar to other SH2 domain complexes, but displays different detail interactions within the phosphotyrosine binding site and in the recognition site for the +3 methionine residue of the peptide, the side chain of which inserts into a particularly deep and narrow pocket which is displaced relative to that of other SH2 domains. The contacts made within this +3 pocket provide the structural basis for the strong selection for methionine at this position which characterizes the SH2 domains of PI3-kinase. Comparison with spectral and structural features of the uncomplexed domain shows that the long BG loop becomes less mobile in the presence of the bound peptide. In contrast, extreme resonance broadening encountered for most residues in the beta D', beta E and beta F strands and associated connecting loops of the domain in the absence of peptide persists in the complex, implying conformational averaging in this part of the molecule on a microsecond-to-millisecond time scale.
==About this Structure==
==About this Structure==
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1PIC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ACE as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Phosphatidylinositol_3-kinase Phosphatidylinositol 3-kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.137 2.7.1.137] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PIC OCA].
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1PIC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=ACE:'>ACE</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Phosphatidylinositol_3-kinase Phosphatidylinositol 3-kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.137 2.7.1.137] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PIC OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Anderson, M.]]
[[Category: Anderson, M.]]
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[[Category: Barratt, D.G.]]
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[[Category: Barratt, D G.]]
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[[Category: Best, J.R.]]
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[[Category: Best, J R.]]
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[[Category: Breeze, A.L.]]
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[[Category: Breeze, A L.]]
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[[Category: Cartlidge, S.A.]]
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[[Category: Cartlidge, S A.]]
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[[Category: Kara, B.V.]]
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[[Category: Kara, B V.]]
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[[Category: Luke, R.W.]]
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[[Category: Luke, R W.]]
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[[Category: Smith, J.C.]]
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[[Category: Smith, J C.]]
[[Category: ACE]]
[[Category: ACE]]
[[Category: complex (phosphotransferase/receptor)]]
[[Category: complex (phosphotransferase/receptor)]]
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[[Category: signal transduction]]
[[Category: signal transduction]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:29:02 2008''

Revision as of 12:29, 21 February 2008


1pic

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PHOSPHATIDYLINOSITOL 3-KINASE, P85-ALPHA SUBUNIT: C-TERMINAL SH2 DOMAIN COMPLEXED WITH A TYR751 PHOSPHOPEPTIDE FROM THE PDGF RECEPTOR, NMR, MINIMIZED MEAN STRUCTURE

Overview

We have determined the solution structure of the C-terminal SH2 domain of the p85 alpha subunit of human phosphatidylinositol (PI) 3-kinase (EC 2.7.1.137) in complex with a phosphorylated tyrosine pentapeptide sequence from the platelet-derived growth factor receptor using heteronuclear nuclear magnetic resonance spectroscopy. Overall, the structure is similar to other SH2 domain complexes, but displays different detail interactions within the phosphotyrosine binding site and in the recognition site for the +3 methionine residue of the peptide, the side chain of which inserts into a particularly deep and narrow pocket which is displaced relative to that of other SH2 domains. The contacts made within this +3 pocket provide the structural basis for the strong selection for methionine at this position which characterizes the SH2 domains of PI3-kinase. Comparison with spectral and structural features of the uncomplexed domain shows that the long BG loop becomes less mobile in the presence of the bound peptide. In contrast, extreme resonance broadening encountered for most residues in the beta D', beta E and beta F strands and associated connecting loops of the domain in the absence of peptide persists in the complex, implying conformational averaging in this part of the molecule on a microsecond-to-millisecond time scale.

About this Structure

1PIC is a Single protein structure of sequence from Homo sapiens with as ligand. Active as Phosphatidylinositol 3-kinase, with EC number 2.7.1.137 Full crystallographic information is available from OCA.

Reference

Structure of a specific peptide complex of the carboxy-terminal SH2 domain from the p85 alpha subunit of phosphatidylinositol 3-kinase., Breeze AL, Kara BV, Barratt DG, Anderson M, Smith JC, Luke RW, Best JR, Cartlidge SA, EMBO J. 1996 Jul 15;15(14):3579-89. PMID:8670861

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