Gene Ontology annotation through association of InterPro records with GO terms
Gene Ontology annotation based on Enzyme Commission mapping
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
A novel Ras-interacting protein required for chemotaxis and cyclic adenosine monophosphate signal relay in Dictyostelium.
Functional overlap of the dictyostelium RasG, RasD and RasB proteins.
Mediation of cell-substratum adhesion by RasG in Dictyostelium.
Expression of activated Ras during Dictyostelium development alters cell localization and changes cell fate.
Chemoattractant-induced Ras activation during Dictyostelium aggregation.
Phg2, a kinase involved in adhesion and focal site modeling in Dictyostelium.
The identification of Dictyostelium phosphoproteins altered in response to the activation of RasG.
Localized Ras signaling at the leading edge regulates PI3K, cell polarity, and directional cell movement.
An activated Ras protein alters cell adhesion by dephosphorylating Dictyostelium DdCAD-1.
Cell motility and SCAR localisation in axenically growing Dictyostelium cells.
Delineation of the roles played by RasG and RasC in cAMP-dependent signal transduction during the early development of Dictyostelium discoideum.
Proteomics fingerprinting of phagosome maturation and evidence for the role of a Galpha during uptake.
Cyclic AMP signalling in Dictyostelium: G-proteins activate separate Ras pathways using specific RasGEFs.
Rap1 activation in response to cAMP occurs downstream of ras activation during Dictyostelium aggregation.
Proteome analysis of Legionella vacuoles purified by magnetic immunoseparation reveals secretory and endosomal GTPases.
Nanovesicles released by Dictyostelium cells: a potential carrier for drug delivery.
A Rap/phosphatidylinositol 3-kinase pathway controls pseudopod formation [corrected].
Ras-related genes in Dictyostelium discoideum.
Ras proteins have multiple functions in vegetative cells of Dictyostelium.
Delineating the core regulatory elements crucial for directed cell migration by examining folic-acid-mediated responses.
Daydreamer, a Ras effector and GSK-3 substrate, is important for directional sensing and cell motility.
Two distinct functions for PI3-kinases in macropinocytosis.
Dictyostelium lipid droplets host novel proteins.
Degradation of activated K-Ras orthologue via K-Ras-specific lysine residues is required for cytokinesis.
RasG signaling is important for optimal folate chemotaxis in Dictyostelium.
Regulation of a LATS-homolog by Ras GTPases is important for the control of cell division.
The novel RacE-binding protein GflB sharpens Ras activity at the leading edge of migrating cells.
The small GTPases Ras and Rap1 bind to and control TORC2 activity.
A Diaphanous-related formin links Ras signaling directly to actin assembly in macropinocytosis and phagocytosis.
Comparative Proteomics of Purified Pathogen Vacuoles Correlates Intracellular Replication of Legionella pneumophila with the Small GTPase Ras-related protein 1 (Rap1).
GPCR-controlled membrane recruitment of negative regulator C2GAP1 locally inhibits Ras signaling for adaptation and long-range chemotaxis.
An endogenous chemorepellent directs cell movement by inhibiting pseudopods at one side of cells.
IQGAP-related protein IqgC suppresses Ras signaling during large-scale endocytosis.
Function of small GTPases in Dictyostelium macropinocytosis.
A chemorepellent inhibits local Ras activation to inhibit pseudopod formation to bias cell movement away from the chemorepellent.
IqgC is a potent regulator of macropinocytosis in the presence of NF1 and its loading to macropinosomes is dependent on RasG.
Leep2A and Leep2B function as a RasGAP complex to regulate macropinosome formation.
Francisella novicida-Containing Vacuole within Dictyostelium discoideum: Isolation and Proteomic Characterization.
The IQGAP-related RasGAP IqgC regulates cell-substratum adhesion in Dictyostelium discoideum.
The Ras association domain of DydA as a specific reporter of activated RasG in Dictyostelium.
Overexpression of an activated rasG gene during growth blocks the initiation of Dictyostelium development.
Dictyostelium RasG is required for normal motility and cytokinesis, but not growth.
Negative influence of RasG on chemoattractant-induced ERK2 phosphorylation in Dictyostelium.