The rab gtpase family
H Stenmark, VM Olkkonen - Genome biology, 2001 - Springer
The Rab family is part of the Ras superfamily of small GTPases. There are at least 60 Rab
genes in the human genome, and a number of Rab GTPases are conserved from yeast to …
genes in the human genome, and a number of Rab GTPases are conserved from yeast to …
Novel aspects of mevalonate pathway inhibitors as antitumor agents
M Thurnher, O Nussbaumer, G Gruenbacher - Clinical Cancer Research, 2012 - AACR
The mevalonate pathway for cholesterol biosynthesis and protein prenylation has been
implicated in various aspects of tumor development and progression. Certain classes of …
implicated in various aspects of tumor development and progression. Certain classes of …
The role of ARF and Rab GTPases in membrane transport
P Chavrier, B Goud - Current opinion in cell biology, 1999 - Elsevier
Two key events of intracellular transport and membrane trafficking in eukaryotic cells, the
formation of transport vesicles and their specific delivery to target membranes, are controlled …
formation of transport vesicles and their specific delivery to target membranes, are controlled …
Thematic review series: lipid posttranslational modifications. geranylgeranylation of Rab GTPases
KF Leung, R Baron, MC Seabra - Journal of lipid research, 2006 - ASBMB
Rab GTPases require special machinery for protein prenylation, which include Rab escort
protein (REP) and Rab geranylgeranyl transferase (RGGT). The current model of Rab …
protein (REP) and Rab geranylgeranyl transferase (RGGT). The current model of Rab …
PRL PTPs: mediators and markers of cancer progression
DC Bessette, D Qiu, CJ Pallen - Cancer and Metastasis Reviews, 2008 - Springer
Aberrant protein tyrosine phosphorylation resulting from the altered activity of protein
tyrosine phosphatases (PTPs) is increasingly being implicated in the genesis and …
tyrosine phosphatases (PTPs) is increasingly being implicated in the genesis and …
Griscelli syndrome: a model system to study vesicular trafficking
M Van Gele, P Dynoodt… - Pigment cell & melanoma …, 2009 - Wiley Online Library
Griscelli syndrome (GS) is a rare autosomal recessive disorder caused by mutations in
either the myosin VA (GS1), RAB27A (GS2) or melanophilin (GS3) genes. The three GS …
either the myosin VA (GS1), RAB27A (GS2) or melanophilin (GS3) genes. The three GS …
RabGDI displacement by DrrA from Legionella is a consequence of its guanine nucleotide exchange activity
Prenylated Rab proteins exist in the cytosol as soluble, high-affinity complexes with GDI that
need to be disrupted for membrane attachment and targeting of Rab proteins. The …
need to be disrupted for membrane attachment and targeting of Rab proteins. The …
[HTML][HTML] Prenylation of Rab GTPases: molecular mechanisms and involvement in genetic disease
Small GTPases of the Rab family regulate membrane transport pathways. More than 50
mammalian Rab proteins are known, many with transport step-specific localisation. Rabs …
mammalian Rab proteins are known, many with transport step-specific localisation. Rabs …
H ermansky–P udlak syndrome: pigmentary and non‐pigmentary defects and their pathogenesis
H ermansky–P udlak syndrome (HPS) is an autosomal recessive and genetically
heterogeneous disorder characterized by oculocutaneous albinism, bleeding tendency, and …
heterogeneous disorder characterized by oculocutaneous albinism, bleeding tendency, and …
The structural and mechanistic basis for recycling of Rab proteins between membrane compartments
RS Goody, A Rak, K Alexandrov - Cellular and Molecular Life Sciences …, 2005 - Springer
Rab proteins are members of the Ras superfamily of GTPases and are key regulators of
intracellular vesicular transport. They undergo a cycle of GTPase activity, and this activity is …
intracellular vesicular transport. They undergo a cycle of GTPase activity, and this activity is …