Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P84077 ARF1 ADP-ribosylation factor 1 (EC 3.6.5.2) Homo sapiens (Human) 181 aa

Protein Details: P84077 (ARF1)

Protein Information
AccessionP84077
Protein NamesADP-ribosylation factor 1 (EC 3.6.5.2)
Gene SymbolARF1
OrganismHomo sapiens (Human)
Length181 aa
IsoformsNo isoforms
Related PMIDs 19137006 31251020
Database SourcesSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MGNIFANLFK11GLFGKKEMRI21LMVGLDAAGK31TTILYKLKLG41EIVTTIPTIG
51-10051FNVETVEYKN61ISFTVWDVGG71QDKIRPLWRH81YFQNTQGLIF91VVDSNDRERV
101-150101NEAREELMRM111LAEDELRDAV121LLVFANKQDL131PNAMNAAEIT141DKLGLHSLRH
151-181151RNWYIQATCA161TSGDGLYEGL171DWLSNQLRNQ181K
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
159 - - -
Deep-Palm: 0.76
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): 0.667
2
LNCaP
Specificity: 0.667
2/2 (100.0%)
1
Jurkat T cell
Specificity: 0.333
1/1 (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
19 R → C 0.001887 SNP Missense Mutation UCEC
19 R → C 0.003460 SNP Missense Mutation CESC
79 R → C 0.002020 SNP Missense Mutation PRAD
79 R → C 0.001887 SNP Missense Mutation UCEC