Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Rab24 is an atypical member of the Rab GTPase family. Deficient GTPase activity, GDP dissociation inhibitor interaction, and prenylation of Rab24 expressed in cultured cells.
-
Human Rab24 is predominantly GTP-bound, has low GTPase activity, is inefficiently prenylated, and is partly membrane-associated.
Structural basis of family-wide Rab GTPase recognition by rabenosyn-5.
Network organization of the human autophagy system.
A reference map of the human binary protein interactome.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Exocytosis of secretory granule membrane proteins
UniProtKB record for human RAB24
-
UniProt summarizes RAB24 as an atypical Rab protein with low GTPase activity, predominant GTP-bound state, basal late-autophagic-vacuole clearance, and by-similarity oocyte meiotic apparatus context.
RAB24 facilitates clearance of autophagic compartments during basal conditions.
Falcon deep research report for RAB24
-
LLM-synthesized literature report agreeing that RAB24 is an atypical Rab with low intrinsic GTPase activity, predominantly GTP-bound, prenylation-dependent membrane targeting, and a late-stage basal-autophagy clearance role; it additionally surfaces the Rab7/RILP late-endosomal degradation interaction (Amaya 2016) and immuno-EM localization to both inner and outer autophagic-vacuole membranes.