1no6

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==Overview==
==Overview==
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Protein tyrosine phosphatase 1B (PTP1B) is an enzyme that downregulates, the insulin receptor. Inhibition of PTP1B is expected to improve insulin, action, and the design of small molecule PTP1B inhibitors to treat type II, diabetes has received considerable attention. In this work, NMR-based, screening identified a nonselective competitive inhibitor of PTP1B. A, second site ligand was also identified by NMR-based screening and then, linked to the catalytic site ligand by rational design. X-ray data, confirmed that the inhibitor bound with the catalytic site in the native, "open" conformation. The final compound displayed excellent potency and, good selectivity over many other phosphatases. The modular approach to, drug design described in this work should be applicable for the design of, potent and selective inhibitors of other therapeutically relevant protein, tyrosine phosphatases.
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Protein tyrosine phosphatase 1B (PTP1B) is an enzyme that downregulates the insulin receptor. Inhibition of PTP1B is expected to improve insulin action, and the design of small molecule PTP1B inhibitors to treat type II diabetes has received considerable attention. In this work, NMR-based screening identified a nonselective competitive inhibitor of PTP1B. A second site ligand was also identified by NMR-based screening and then linked to the catalytic site ligand by rational design. X-ray data confirmed that the inhibitor bound with the catalytic site in the native, "open" conformation. The final compound displayed excellent potency and good selectivity over many other phosphatases. The modular approach to drug design described in this work should be applicable for the design of potent and selective inhibitors of other therapeutically relevant protein tyrosine phosphatases.
==Disease==
==Disease==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Abad-Zapatero, C.]]
[[Category: Abad-Zapatero, C.]]
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[[Category: Ballaron, S.J.]]
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[[Category: Ballaron, S J.]]
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[[Category: Fesik, S.W.]]
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[[Category: Fesik, S W.]]
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[[Category: Hajduk, P.J.]]
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[[Category: Hajduk, P J.]]
[[Category: Huang, F.]]
[[Category: Huang, F.]]
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[[Category: Hutchins, C.W.]]
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[[Category: Hutchins, C W.]]
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[[Category: Jirousek, M.R.]]
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[[Category: Jirousek, M R.]]
[[Category: Liang, H.]]
[[Category: Liang, H.]]
[[Category: Liu, G.]]
[[Category: Liu, G.]]
[[Category: Lubben, T.]]
[[Category: Lubben, T.]]
[[Category: Pei, Z.]]
[[Category: Pei, Z.]]
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[[Category: Stashko, M.A.]]
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[[Category: Stashko, M A.]]
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[[Category: Szczepankiewicz, B.G.]]
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[[Category: Szczepankiewicz, B G.]]
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[[Category: Trevillyan, J.M.]]
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[[Category: Trevillyan, J M.]]
[[Category: Xin, Z.]]
[[Category: Xin, Z.]]
[[Category: 794]]
[[Category: 794]]
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[[Category: protein tyrosine phosphatase fold]]
[[Category: protein tyrosine phosphatase fold]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 16:29:54 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:08:10 2008''

Revision as of 12:08, 21 February 2008


1no6, resolution 2.40Å

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Potent, Selective Protein Tyrosine Phosphatase 1B Inhibitor Compound 5 Using a Linked-Fragment Strategy

Contents

Overview

Protein tyrosine phosphatase 1B (PTP1B) is an enzyme that downregulates the insulin receptor. Inhibition of PTP1B is expected to improve insulin action, and the design of small molecule PTP1B inhibitors to treat type II diabetes has received considerable attention. In this work, NMR-based screening identified a nonselective competitive inhibitor of PTP1B. A second site ligand was also identified by NMR-based screening and then linked to the catalytic site ligand by rational design. X-ray data confirmed that the inhibitor bound with the catalytic site in the native, "open" conformation. The final compound displayed excellent potency and good selectivity over many other phosphatases. The modular approach to drug design described in this work should be applicable for the design of potent and selective inhibitors of other therapeutically relevant protein tyrosine phosphatases.

Disease

Known diseases associated with this structure: Abdominal body fat distribution, modifier of OMIM:[176885], Insulin resistance, susceptibility to OMIM:[176885]

About this Structure

1NO6 is a Single protein structure of sequence from Homo sapiens with as ligand. Active as Protein-tyrosine-phosphatase, with EC number 3.1.3.48 Full crystallographic information is available from OCA.

Reference

Discovery of a potent, selective protein tyrosine phosphatase 1B inhibitor using a linked-fragment strategy., Szczepankiewicz BG, Liu G, Hajduk PJ, Abad-Zapatero C, Pei Z, Xin Z, Lubben TH, Trevillyan JM, Stashko MA, Ballaron SJ, Liang H, Huang F, Hutchins CW, Fesik SW, Jirousek MR, J Am Chem Soc. 2003 Apr 9;125(14):4087-96. PMID:12670229

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