Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A8I5QJ95 ARL6IP6 ADP ribosylation factor like GTPase … Homo sapiens (Human) 43 aa

Protein Details: A0A8I5QJ95 (ARL6IP6)

Protein Information
AccessionA0A8I5QJ95
Protein NamesADP ribosylation factor like GTPase 6 interacting protein 6
Gene SymbolARL6IP6
OrganismHomo sapiens (Human)
Length43 aa
IsoformsNo isoforms
Related PMIDs 19137006 32944167
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-431MFPPTPLSPA11RFKKLTGHSF21HMGYSMAILN31GIVAALTVAW41CLM
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
41 - - -
GPS-Palm: 0.98
Deep-Palm: 0.01
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): 0.500
2
Jurkat T cell
Specificity: 0.500
2/2 (100.0%)
2
PC3
Specificity: 0.500
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
48 C → Afs*83 0.001969 DEL Frame Shift Del HNSC
89 G → C 0.001887 SNP Missense Mutation UCEC
169 S → C 0.001969 SNP Missense Mutation HNSC
172 W → C 0.001014 SNP Missense Mutation BRCA