1u32: Difference between revisions

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New page: left|200px<br /> <applet load="1u32" size="450" color="white" frame="true" align="right" spinBox="true" caption="1u32, resolution 2.00Å" /> '''Crystal structure o...
 
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[[Image:1u32.gif|left|200px]]<br />
[[Image:1u32.gif|left|200px]]<br /><applet load="1u32" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1u32" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1u32, resolution 2.00&Aring;" />
caption="1u32, resolution 2.00&Aring;" />
'''Crystal structure of a Protein Phosphatase-1: Calcineurin Hybrid Bound to Okadaic Acid'''<br />
'''Crystal structure of a Protein Phosphatase-1: Calcineurin Hybrid Bound to Okadaic Acid'''<br />


==Overview==
==Overview==
Protein phosphatase-1 and protein phosphatase-2B (calcineurin) are, eukaryotic serine/threonine phosphatases that share 40% sequence identity, in their catalytic subunits. Despite the similarities in sequence, these, phosphatases are widely divergent when it comes to inhibition by natural, product toxins, such as microcystin-LR and okadaic acid. The most, prominent region of non-conserved sequence between these phosphatases, corresponds to the beta12-beta13 loop of protein phosphatase-1, and the L7, loop of toxin-resistant calcineurin. In the present study, mutagenesis of, residues 273-277 of the beta12-beta13 loop of the protein phosphatase-1, catalytic subunit (PP-1c) to the corresponding residues in calcineurin, (312-316), resulted in a chimeric mutant that showed a decrease in, sensitivity to microcystin-LR, okadaic acid, and the endogenous PP-1c, inhibitor protein inhibitor-2. A crystal structure of the chimeric mutant, in complex with okadaic acid was determined to 2.0-A resolution. The, beta12-beta13 loop region of the mutant superimposes closely with that of, wild-type PP-1c bound to okadaic acid. Systematic mutation of each residue, in the beta12-beta13 loop of PP-1c showed that a single amino acid change, (C273L) was the most influential in mediating sensitivity of PP-1c to, toxins. Taken together, these data indicate that it is an individual amino, acid residue substitution and not a change in the overall beta12-beta13, loop conformation of protein phosphatase-1 that contributes to disrupting, important interactions with inhibitors such as microcystin-LR and okadaic, acid.
Protein phosphatase-1 and protein phosphatase-2B (calcineurin) are eukaryotic serine/threonine phosphatases that share 40% sequence identity in their catalytic subunits. Despite the similarities in sequence, these phosphatases are widely divergent when it comes to inhibition by natural product toxins, such as microcystin-LR and okadaic acid. The most prominent region of non-conserved sequence between these phosphatases corresponds to the beta12-beta13 loop of protein phosphatase-1, and the L7 loop of toxin-resistant calcineurin. In the present study, mutagenesis of residues 273-277 of the beta12-beta13 loop of the protein phosphatase-1 catalytic subunit (PP-1c) to the corresponding residues in calcineurin (312-316), resulted in a chimeric mutant that showed a decrease in sensitivity to microcystin-LR, okadaic acid, and the endogenous PP-1c inhibitor protein inhibitor-2. A crystal structure of the chimeric mutant in complex with okadaic acid was determined to 2.0-A resolution. The beta12-beta13 loop region of the mutant superimposes closely with that of wild-type PP-1c bound to okadaic acid. Systematic mutation of each residue in the beta12-beta13 loop of PP-1c showed that a single amino acid change (C273L) was the most influential in mediating sensitivity of PP-1c to toxins. Taken together, these data indicate that it is an individual amino acid residue substitution and not a change in the overall beta12-beta13 loop conformation of protein phosphatase-1 that contributes to disrupting important interactions with inhibitors such as microcystin-LR and okadaic acid.


==About this Structure==
==About this Structure==
1U32 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 MN, OKA and BME as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Phosphoprotein_phosphatase Phosphoprotein phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.16 3.1.3.16] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1U32 OCA].  
1U32 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=MN:'>MN</scene>, <scene name='pdbligand=OKA:'>OKA</scene> and <scene name='pdbligand=BME:'>BME</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Phosphoprotein_phosphatase Phosphoprotein phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.16 3.1.3.16] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U32 OCA].  


==Reference==
==Reference==
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[[Category: Phosphoprotein phosphatase]]
[[Category: Phosphoprotein phosphatase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Cherney, M.M.]]
[[Category: Cherney, M M.]]
[[Category: Holmes, C.F.B.]]
[[Category: Holmes, C F.B.]]
[[Category: James, M.N.G.]]
[[Category: James, M N.G.]]
[[Category: Luu, H.A.]]
[[Category: Luu, H A.]]
[[Category: Maynes, J.T.]]
[[Category: Maynes, J T.]]
[[Category: Perreault, K.R.]]
[[Category: Perreault, K R.]]
[[Category: BME]]
[[Category: BME]]
[[Category: MN]]
[[Category: MN]]
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[[Category: hydrolase]]
[[Category: hydrolase]]


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