4.7 Review

Structure and dynamic regulation of Src-family kinases

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 65, Issue 19, Pages 3058-3073

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-008-8122-2

Keywords

Src-family kinases; SH3 domain; SH2 domain; hydrogen exchange mass spectrometry; Gaussian Network Model

Funding

  1. National Institutes of Health [CA081398, CA101828, GM070590]
  2. Barnett Institute [917]
  3. NATIONAL CANCER INSTITUTE [K01CA111633, R01CA081398, R01CA101828] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM070590] Funding Source: NIH RePORTER

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Src-family kinases are modular signaling proteins involved in a diverse array of cellular processes. All members of the Src family share the same domain organization, with modular SH3, SH2 and kinase domains followed by a C-terminal negative regulatory tail. X-ray crystallographic analyses of several Src family members have revealed critical roles for the SH3 and SH2 domains in the down-regulation of the kinase domain. This review focuses on biological, biophysical, and computational studies that reveal conformationally distinct active states within this unique kinase family.

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