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

被引:85
作者
Biondi, RM [1 ]
机构
[1] Uniklin Homburg, D-66421 Homburg, Germany
关键词
D O I
10.1016/j.tibs.2004.01.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:136 / 142
页数:7
相关论文
共 70 条
  • [1] Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha
    Alessi, DR
    James, SR
    Downes, CP
    Holmes, AB
    Gaffney, PRJ
    Reese, CB
    Cohen, P
    [J]. CURRENT BIOLOGY, 1997, 7 (04) : 261 - 269
  • [2] 3 Phosphoinositide-dependent protein kinase 1 (PDK1) phosphorylates and activates the p70 S6 kinase in vivo and in vitro
    Alessi, DR
    Kozlowski, MT
    Weng, QP
    Morrice, N
    Avruch, J
    [J]. CURRENT BIOLOGY, 1998, 8 (02) : 69 - 81
  • [3] Further evidence that 3-phosphoinositide-dependent protein kinase-1 (PDK1) is required for the stability and phosphorylation of protein kinase C (PKC) isoforms
    Balendran, A
    Hare, GR
    Kieloch, A
    Williams, MR
    Alessi, DR
    [J]. FEBS LETTERS, 2000, 484 (03) : 217 - 223
  • [4] A 3-phosphoinositide-dependent protein kinase-1 (PDK1) docking site is required for the phosphorylation of protein kinase Cζ (PKCζ) and PKC-related kinase 2 by PDK1
    Balendran, A
    Biondi, RM
    Cheung, PCF
    Casamayor, A
    Deak, M
    Alessi, DR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (27) : 20806 - 20813
  • [5] Evidence that 3-phosphoinositide-dependent protein kinase-1 mediates phosphorylation of p70 56 kinase in vivo at Thr-412 as well as Thr-252
    Balendran, A
    Currie, R
    Armstrong, CG
    Avruch, J
    Alessi, DR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) : 37400 - 37406
  • [6] Akt forms an intracellular complex with heat shock protein 90 (Hsp90) and Cdc37 and is destabilized by inhibitors of Hsp90 function
    Basso, AD
    Solit, DB
    Chiosis, G
    Giri, B
    Tsichlis, P
    Rosen, N
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (42) : 39858 - 39866
  • [7] Intracellular signalling: PDK1 - a kinase at the hub of things
    Belham, C
    Wu, SL
    Avruch, J
    [J]. CURRENT BIOLOGY, 1999, 9 (03) : R93 - R96
  • [8] The PIF-binding pocket in PDK1 is essential for activation of S6K and SGK, but not PKB
    Biondi, RM
    Kieloch, A
    Currie, RA
    Deak, M
    Alessi, DR
    [J]. EMBO JOURNAL, 2001, 20 (16) : 4380 - 4390
  • [9] High resolution crystal structure of the human PDK1 catalytic domain defines the regulatory phosphopeptide docking site
    Biondi, RM
    Komander, D
    Thomas, CC
    Lizcano, JM
    Deak, M
    Alessi, DR
    van Aalten, DMF
    [J]. EMBO JOURNAL, 2002, 21 (16) : 4219 - 4228
  • [10] Identification of a pocket in the PDK1 kinase domain that interacts with PIF and the C-terminal residues of PKA
    Biondi, RM
    Cheung, PCF
    Casamayor, A
    Deak, M
    Currie, RA
    Alessi, DR
    [J]. EMBO JOURNAL, 2000, 19 (05) : 979 - 988