共 55 条
Mechanisms of action of Rab proteins, key regulators of intracellular vesicular transport
被引:57
作者:

Goody, Roger Sidney
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h-index: 0
机构:
Max Planck Inst Mol Physiol, Dept Struct Biochem, Otto Hahn Str 11, D-44227 Dortmund, Germany Max Planck Inst Mol Physiol, Dept Struct Biochem, Otto Hahn Str 11, D-44227 Dortmund, Germany

Mueller, Matthias Philipp
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机构:
Max Planck Inst Mol Physiol, Dept Struct Biochem, Otto Hahn Str 11, D-44227 Dortmund, Germany Max Planck Inst Mol Physiol, Dept Struct Biochem, Otto Hahn Str 11, D-44227 Dortmund, Germany

Wu, Yao-Wen
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h-index: 0
机构:
Max Planck Gesell, Chem Genom Ctr, D-44227 Dortmund, Germany Max Planck Inst Mol Physiol, Dept Struct Biochem, Otto Hahn Str 11, D-44227 Dortmund, Germany
机构:
[1] Max Planck Inst Mol Physiol, Dept Struct Biochem, Otto Hahn Str 11, D-44227 Dortmund, Germany
[2] Max Planck Gesell, Chem Genom Ctr, D-44227 Dortmund, Germany
关键词:
effectors;
GAPs;
GEFs;
GTPases;
Legionella;
Rabs;
targeting;
GDP-DISSOCIATION INHIBITOR;
C-TERMINAL DOMAIN;
SMALL GTPASE RAB1;
NUCLEOTIDE EXCHANGE;
PHOSPHATIDYLINOSITOL;
4-PHOSPHATE;
POSTTRANSLATIONAL MODIFICATIONS;
EFFECTOR PROTEIN;
STRUCTURAL BASIS;
LEGIONELLA;
COMPLEX;
D O I:
10.1515/hsz-2016-0274
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:
Our understanding of the manner in which Rab proteins regulate intracellular vesicular transport has progressed remarkably in the last one or two decades by application of a wide spectrum of biochemical, biophysical and cell biological methods, augmented by the methods of chemical biology. Important additional insights have arisen from examination of the manner in which certain bacteria can manipulate vesicular transport mechanisms. The progress in these areas is summarized here.
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页码:565 / 575
页数:11
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