Publication:
The Cdc42 Cys81Tyr Mutation: Impact On Guanosine Triphosphatase (Gtpase) Activation Status And Its Cellular Functions

dc.contributor.authorChong, Chien Fung
dc.date.accessioned2026-06-12T07:57:12Z
dc.date.available2026-06-12T07:57:12Z
dc.date.issued2025-08
dc.description.abstractMutations in small Rho guanine triphosphatase (GTPase) have been increasingly associated with various diseases. One of the members is Cdc42, a key regulator of cellular signalling, cytoskeletal organization, and immune responses by cycling between an active GTP-bound and an inactive GDP-bound states. A novel cysteine-to-tyrosine substitution at residue 81 (C81Y) within the β4 segment of Cdc42 has been identified in patients with concurrent primary immunodeficiency (PID) and Hodgkin's lymphoma. Notably, emerging evidence suggests that this mutation disrupts Cdc42 structure-function relationship, potentially impairing immune signalling, altering cytokine secretion profiles, and driving oncogenesis. Yet, the pathogenic roles of Cdc42 C81Y remains poorly understood. This study investigates its structural and biochemical impact, hypothesizing that it disrupts GDP/GTP cycling, post-translational modification, and downstream signalling, contributing to disease pathogenesis.
dc.identifier.urihttps://erepo.usm.my/handle/123456789/24370
dc.language.isoen
dc.subjectCdc42 Cys81Tyr Mutation
dc.subjectImpact On Guanosine Triphosphatase (Gtpase) Activation Status And Its Cellular Functions
dc.titleThe Cdc42 Cys81Tyr Mutation: Impact On Guanosine Triphosphatase (Gtpase) Activation Status And Its Cellular Functions
dc.typeResource Types::text::thesis::doctoral thesis
dspace.entity.typePublication
oairecerif.author.affiliationUniversiti Sains Malaysia
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