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| - | [[Image:3bm8.jpg|left|200px]] | + | {{Seed}} |
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| | {{STRUCTURE_3bm8| PDB=3bm8 | SCENE= }} | | {{STRUCTURE_3bm8| PDB=3bm8 | SCENE= }} |
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| - | '''crystal structure of YopH mutant D356A complexed with irreversible inhibitor PVSN'''
| + | ===crystal structure of YopH mutant D356A complexed with irreversible inhibitor PVSN=== |
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| - | ==Overview==
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| - | Protein tyrosine phosphatases (PTPs) play key roles in the regulation of normal and pathological processes ranging from cell proliferation, differentiation, metabolism, and survival to many human diseases including cancer and diabetes. Functional studies of PTP can be greatly facilitated by small molecule probes that covalently label the active site of a PTP through an activity-dependent chemical reaction. In this article, we characterize phenyl vinyl sulfonate (PVSN) and phenyl vinyl sulfone (PVS) as a new class of mechanism-based PTP probes. PVSN and PVS inactivate a broad range of PTPs in a time- and concentration-dependent fashion. The PVSN- and PVS-mediated PTP inactivation is active site-directed and irreversible, resulting from a Michael addition of the active-site Cys Sgamma onto the terminal carbon of the vinyl group. Structural and mechanistic analyses reveal the molecular basis for the preference of PVSN/PVS toward the PTPs, which lies in the ability of PVSN and PVS to engage the conserved structural and catalytic machinery of the PTP active site. In contrast to early alpha-bromobenzyl phosphonate-based probes, PVSN and PVS are resistant to solvolysis and are cell-permeable and thus hold promise for in vivo applications. Collectively, these properties bode well for the development of aryl vinyl sulfonate/sulfone-based PTP probes to interrogate PTP activity in complex proteomes.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_18528979}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 18528979 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_18528979}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Secreted]] | | [[Category: Secreted]] |
| | [[Category: Virulence]] | | [[Category: Virulence]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 18 12:08:24 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 9 10:09:49 2008'' |
Revision as of 07:09, 9 July 2008
Template:STRUCTURE 3bm8
crystal structure of YopH mutant D356A complexed with irreversible inhibitor PVSN
Template:ABSTRACT PUBMED 18528979
About this Structure
3BM8 is a Single protein structure of sequence from Yersinia enterocolitica. Full crystallographic information is available from OCA.
Reference
Aryl Vinyl Sulfonates and Sulfones as Active Site-Directed and Mechanism-Based Probes for Protein Tyrosine Phosphatases., Liu S, Zhou B, Yang H, He Y, Jiang ZX, Kumar S, Wu L, Zhang ZY, J Am Chem Soc. 2008 Jun 4;. PMID:18528979
Page seeded by OCA on Wed Jul 9 10:09:49 2008
