Target intelligence / Profile preview

RAS p21 protein activator 4B (RASA4B)

Target
RASA4B
Molecular classification
Enzyme (specifically, GTPase-activating protein/GAP), Signal transduction regulator, Metal ion and phospholipid binding protein
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Overview

RAS p21 protein activator 4B (RASA4B) is a Ca2+-dependent GTPase-activating protein that dampens Ras protein signal transduction by promoting the conversion of Ras from its active GTP-bound state to an inactive GDP-bound form. This protein localizes to the cytosol and plasma membrane, especially upon increased intracellular calcium, and participates in the negative regulation of the Ras-MAPK signaling pathway. RASA4B activities are important for control of cell proliferation, differentiation, and apoptosis; aberrant regulation or mutation of RASA4B is implicated in tumorigenesis and other pathological conditions where Ras signaling is dysregulated

Other names
RASA4BRas GTPase-activating protein 4BRAS p21 protein activator 4B
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Mechanism of action

For drugs or research agents, mechanisms would include inhibition of RASA4B activity or modulation of its expression, leading to altered Ras pathway signaling

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Biological functions

Negative regulation of Ras signal transductionGTPase activator activity (promoting inactivation of Ras proteins)Cellular response to calcium ionsIntracellular signal transductionRegulation of cell proliferation, differentiation, and apoptosis
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Disease associations

Cancer (implicated in several cancer types through aberrant Ras signaling)Potential association with Hemoglobin H disease
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Safety considerations

No clinical safety concerns are documented for direct modulation of RASA4B, as no drugs are currently in clinical use; theoretical concerns would relate to disruption of cell proliferation and apoptosis regulation
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Interacting drugs

There are currently no approved drugs directly targeting RASA4B; however, research tools such as knockout cell lines and antibodies are used to study its function
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Biomarkers

No established biomarkers for clinical patient selection or efficacy monitoring are reported for RASA4B specifically; Ras pathway activity may provide indirect readouts

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