1oeo
From Proteopedia
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| - | [[Image:1oeo. | + | [[Image:1oeo.jpg|left|200px]]<br /><applet load="1oeo" size="450" color="white" frame="true" align="right" spinBox="true" |
| - | <applet load="1oeo" size="450" color="white" frame="true" align="right" spinBox="true" | + | |
caption="1oeo, resolution 2.15Å" /> | caption="1oeo, resolution 2.15Å" /> | ||
'''PTP1B WITH THE CATALYTIC CYSTEINE OXIDIZED TO SULFONIC ACID'''<br /> | '''PTP1B WITH THE CATALYTIC CYSTEINE OXIDIZED TO SULFONIC ACID'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1OEO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Protein-tyrosine-phosphatase Protein-tyrosine-phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.48 3.1.3.48] | + | 1OEO is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Protein-tyrosine-phosphatase Protein-tyrosine-phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.48 3.1.3.48] Known structural/functional Site: <scene name='pdbsite=CAT:Oxidized To Sulfonic Acid'>CAT</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OEO OCA]. |
==Reference== | ==Reference== | ||
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[[Category: phosphorylation]] | [[Category: phosphorylation]] | ||
| - | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 17:38:54 2007'' |
Revision as of 15:29, 18 December 2007
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PTP1B WITH THE CATALYTIC CYSTEINE OXIDIZED TO SULFONIC ACID
Contents |
Overview
The second messenger hydrogen peroxide is required for optimal activation, of numerous signal transduction pathways, particularly those mediated by, protein tyrosine kinases. One mechanism by which hydrogen peroxide, regulates cellular processes is the transient inhibition of protein, tyrosine phosphatases through the reversible oxidization of their, catalytic cysteine, which suppresses protein dephosphorylation. Here we, describe a structural analysis of the redox-dependent regulation of, protein tyrosine phosphatase 1B (PTP1B), which is reversibly inhibited by, oxidation after cells are stimulated with insulin and epidermal growth, factor. The sulphenic acid intermediate produced in response to PTP1B, oxidation is rapidly converted into a previously unknown sulphenyl-amide, species, in which the sulphur atom of the catalytic cysteine is covalently, linked to the main chain nitrogen of an adjacent residue. Oxidation of, PTP1B to the sulphenyl-amide form is accompanied by large conformational, changes in the catalytic site that inhibit substrate binding. We propose, that this unusual protein modification both protects the active-site, cysteine residue of PTP1B from irreversible oxidation to sulphonic acid, and permits redox regulation of the enzyme by promoting its reversible, reduction by thiols.
Disease
Known diseases associated with this structure: Abdominal body fat distribution, modifier of OMIM:[176885], Insulin resistance, susceptibility to OMIM:[176885]
About this Structure
1OEO is a Single protein structure of sequence from Homo sapiens. Active as Protein-tyrosine-phosphatase, with EC number 3.1.3.48 Known structural/functional Site: . Full crystallographic information is available from OCA.
Reference
Redox regulation of protein tyrosine phosphatase 1B involves a sulphenyl-amide intermediate., Salmeen A, Andersen JN, Myers MP, Meng TC, Hinks JA, Tonks NK, Barford D, Nature. 2003 Jun 12;423(6941):769-73. PMID:12802338
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