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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
F8WET9 RHOQ Ras homolog family member Q Homo sapiens (Human) 50 aa

Protein Details: F8WET9 (RHOQ)

Protein Information
AccessionF8WET9
Protein NamesRas homolog family member Q
Gene SymbolRHOQ
OrganismHomo sapiens (Human)
Length50 aa
IsoformsNo isoforms
Related PMIDs 31251020
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MAHGPGALML11KCVVVGDGAV21GKTCLLMSYA31NDAFPEEYVP41TVFDHYAGRL
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
12 SWISSPALM DBPTM CYSMODDB Ras family P-loop containing nucleoside triphosphate hydrolase Small GTPase -
cerebral cortex (36430497)
GPS-Palm: 0.75
Deep-Palm: 0.93
24 P-loop containing nucleoside triphosphate hydrolase Small GTPase Rho Small GTPase Transforming protein P21 ras signature - -
Deep-Palm: 0.93
Score Interpretation:
GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
2
LNCaP
Specificity: 1.000
2/2 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). Blue bars: Literature data, Orange bars: Mass Spectrometry data. The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
159 C → C 0.002506 SNP Silent COAD
? ? → ? 0.002033 SNP Missense Mutation LUSC