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Structural features of mammalian histidine decarboxylase reveal the basis for specific inhibition

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 157, 期 1, 页码 4-13

出版社

WILEY
DOI: 10.1111/j.1476-5381.2009.00219.x

关键词

histamine; histidine decarboxylase; QM; MM; virtual screening; homology modelling; molecular dynamics

资金

  1. Ministerio de Ciencia e Innovacion [SAF2008-02522]
  2. Comunidad de Madrid [SBIO-0214-2006]

向作者/读者索取更多资源

For a long time the structural and molecular features of mammalian histidine decarboxylase (EC 4.1.1.22), the enzyme that produces histamine, have evaded characterization. We overcome the experimental problems for the study of this enzyme by using a computer-based modelling and simulation approach, and have now the conditions to use histidine decarboxylase as a target in histamine pharmacology. In this review, we present the recent (last 5 years) advances in the structure-function relationship of histidine decarboxylase and the strategy for the discovery of new drugs.

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