Literature DB >> 15003271

Phosphoinositide-dependent protein kinase 1, a sensor of protein conformation.

Ricardo M Biondi1.   

Abstract

Phosphoinositide-dependent protein kinase 1 (PDK1) is a protein kinase that phosphorylates and activates several other protein kinases from the AGC group (which includes PKA, PKG and PKC), to which PDK1 also belongs. Recent data suggests that PDK1 specificity is achieved by regulation of its interaction with substrates and supports a rather simple model explaining how PDK1 interacts with different substrates. The data further suggests that PDK1 interacts with its substrates when they are in a particular conformation (inactive). PDK1 has the ability to recognize, interact with and phosphorylate specific substrate conformations and thus sets PDK1 at the centre of a protein conformation sensor mechanism. The PDK1-substrate interaction model describes, at a molecular level, the mechanism used by PDK1 to sense the conformation of its substrates.

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Year:  2004        PMID: 15003271     DOI: 10.1016/j.tibs.2004.01.005

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  40 in total

1.  Allosteric activation of the protein kinase PDK1 with low molecular weight compounds.

Authors:  Matthias Engel; Valerie Hindie; Laura A Lopez-Garcia; Adriana Stroba; Francis Schaeffer; Iris Adrian; Jochen Imig; Leila Idrissova; Wolfgang Nastainczyk; Stefan Zeuzem; Pedro M Alzari; Rolf W Hartmann; Albrecht Piiper; Ricardo M Biondi
Journal:  EMBO J       Date:  2006-11-16       Impact factor: 11.598

Review 2.  Substrate and docking interactions in serine/threonine protein kinases.

Authors:  Elizabeth J Goldsmith; Radha Akella; Xiaoshan Min; Tianjun Zhou; John M Humphreys
Journal:  Chem Rev       Date:  2007-10-19       Impact factor: 60.622

3.  Adi3 is a Pdk1-interacting AGC kinase that negatively regulates plant cell death.

Authors:  Timothy P Devarenne; Sophia K Ekengren; Kerry F Pedley; Gregory B Martin
Journal:  EMBO J       Date:  2005-12-15       Impact factor: 11.598

Review 4.  Regulation of mRNA translation in renal physiology and disease.

Authors:  Balakuntalam S Kasinath; Denis Feliers; Kavithalakshmi Sataranatarajan; Goutam Ghosh Choudhury; Myung Ja Lee; Meenalakshmi M Mariappan
Journal:  Am J Physiol Renal Physiol       Date:  2009-06-17

5.  Structure and allosteric effects of low-molecular-weight activators on the protein kinase PDK1.

Authors:  Valerie Hindie; Adriana Stroba; Hua Zhang; Laura A Lopez-Garcia; Leila Idrissova; Stefan Zeuzem; Daniel Hirschberg; Francis Schaeffer; Thomas J D Jørgensen; Matthias Engel; Pedro M Alzari; Ricardo M Biondi
Journal:  Nat Chem Biol       Date:  2009-08-30       Impact factor: 15.040

6.  Phosphoinositide-dependent phosphorylation of PDK1 regulates nuclear translocation.

Authors:  Michael P Scheid; Michael Parsons; James R Woodgett
Journal:  Mol Cell Biol       Date:  2005-03       Impact factor: 4.272

7.  Activation of hematopoietic progenitor kinase 1 involves relocation, autophosphorylation, and transphosphorylation by protein kinase D1.

Authors:  Rüdiger Arnold; Irene M Patzak; Brit Neuhaus; Sadia Vancauwenbergh; André Veillette; Johan Van Lint; Friedemann Kiefer
Journal:  Mol Cell Biol       Date:  2005-03       Impact factor: 4.272

8.  The mammalian target of rapamycin complex 2 controls folding and stability of Akt and protein kinase C.

Authors:  Valeria Facchinetti; Weiming Ouyang; Hua Wei; Nelyn Soto; Adam Lazorchak; Christine Gould; Carolyn Lowry; Alexandra C Newton; Yuxin Mao; Robert Q Miao; William C Sessa; Jun Qin; Pumin Zhang; Bing Su; Estela Jacinto
Journal:  EMBO J       Date:  2008-06-19       Impact factor: 11.598

9.  Loss of post-translational modification sites in disease.

Authors:  Shuyan Li; Lilia M Iakoucheva; Sean D Mooney; Predrag Radivojac
Journal:  Pac Symp Biocomput       Date:  2010

Review 10.  Role of AGC kinases in plant growth and stress responses.

Authors:  Ana Victoria Garcia; Mohamed Al-Yousif; Heribert Hirt
Journal:  Cell Mol Life Sci       Date:  2012-07-31       Impact factor: 9.261

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