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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Structural Analysis of Inhibitor Binding to CAMKK1 Identifies Features Necessary for Design of Specific Inhibitors

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Autor(es):
Santiago, Andre da Silva [1] ; Counago, Rafael M. [1, 2] ; Ramos, Priscila Zonzini [1] ; Godoi, Paulo H. C. [1] ; Massirer, Katlin B. [1, 2] ; Gileadi, Opher [3] ; Elkins, Jonathan M. [3, 1]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas, Struct Genom Consortium, Cidade Univ Zeferino Vaz, Av Dr Andre Tosello 550, BR-13083886 Campinas, SP - Brazil
[2] Univ Estadual Campinas, CBMEG, Ctr Mol Biol & Genet Engn, Av Candido Rondon 400, BR-13083875 Campinas, SP - Brazil
[3] Univ Oxford, Struct Genom Consortium, Old Rd Campus Res Bldg, Roosevelt Dr, Oxford OX3 7DQ - England
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: SCIENTIFIC REPORTS; v. 8, OCT 4 2018.
Citações Web of Science: 0
Resumo

The calcium/calmodulin-dependent protein kinases (CAMKKs) are upstream activators of CAMK1 and CAMK4 signalling and have important functions in neural development, maintenance and signalling, as well as in other aspects of biology such as Ca2+ signalling in the cardiovascular system. To support the development of specific inhibitors of CAMKKs we have determined the crystal structure of CAMKK1 with two ATP-competitive inhibitors. The structures reveal small but exploitable differences between CAMKK1 and CAMKK2, despite the high sequence identity, which could be used in the generation of specific inhibitors. Screening of a kinase inhibitor library revealed molecules that bind potently to CAMKK1. Isothermal titration calorimetry revealed that the most potent inhibitors had binding energies largely dependent on favourable enthalpy. Together, the data provide a foundation for future inhibitor development activities. (AU)

Processo FAPESP: 13/50724-5 - Centro de Biologia Química de Proteínas Quinases: alavancando desenvolvimento de fármacos através de pesquisa de acesso aberto
Beneficiário:Paulo Arruda
Linha de fomento: Auxílio à Pesquisa - Parceria para Inovação Tecnológica - PITE