Human liver glycogen phosphorylase inhibitors bind at a new allosteric site (Q24290218)

identical protein binding

GOA release 2020-03-11

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GOA release 2020-03-11

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V L Rath

1

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M Ammirati

2

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D E Danley

3

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J L Ekstrom

4

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E M Gibbs

5

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T R Hynes

6

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A M Mathiowetz

7

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R K McPherson

8

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T V Olson

9

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J L Treadway

10

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D J Hoover

Pharmacologic therapy for type 2 diabetes mellitus

11

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language of work or name

English

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publication date

September 2000

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published in

Chemistry and Biology

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volume

7

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issue

9

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page(s)

677-82

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cites work

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The family of glycogen phosphorylases: structure and function

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Regulation of the dephosphorylation of glycogen phosphorylase a and synthase b by glucose and caffeine in isolated hepatocytes

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Glucose analogue inhibitors of glycogen phosphorylase: the design of potential drugs for diabetes

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The structure of a glycogen phosphorylase glucopyranose spirohydantoin complex at 1.8 A resolution and 100 K: the role of the water structure and its contribution to binding

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The structure of glycogen phosphorylase b with an alkyldihydropyridine-dicarboxylic acid compound, a novel and potent inhibitor

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Inhibition of glycogenolysis in primary rat hepatocytes by 1, 4-dideoxy-1,4-imino-D-arabinitol

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Discovery of a human liver glycogen phosphorylase inhibitor that lowers blood glucose in vivo

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Indole-2-carboxamide inhibitors of human liver glycogen phosphorylase

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A new allosteric site in glycogen phosphorylase b as a target for drug interactions

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Cation-pi interactions in structural biology

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ON THE NATURE OF ALLOSTERIC TRANSITIONS: A PLAUSIBLE MODEL

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On the attribution and additivity of binding energies

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N-acetyl-beta-D-glucopyranosylamine: a potent T-state inhibitor of glycogen phosphorylase. A comparison with alpha-D-glucose.

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Improved methods for building protein models in electron density maps and the location of errors in these models

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Mitogen-activated protein kinase kinase inhibition does not block the stimulation of glucose utilization by insulin

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