Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
E9PK34 ARCN1 Coatomer subunit delta Homo sapiens (Human) 83 aa

Protein Details: E9PK34 (ARCN1)

Protein Information
AccessionE9PK34
Protein NamesCoatomer subunit delta
Gene SymbolARCN1
OrganismHomo sapiens (Human)
Length83 aa
IsoformsNo isoforms
Related PMIDs 22496122
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MVLLAAAVCT11KAGKAIVSRQ21FVEMTRTRIE31GLLAAFPKLM41NTGKQHTFVE
51-8351TESIRMSSVL61FPYQFIPSSL71CQVVFLSGPV81LPV
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
9 SWISSPALM DBPTM CYSMODDB Coatomer delta subunit - -
GPS-Palm: 0.96
Deep-Palm: 0.31
71 - - -
Deep-Palm: 0.18
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
1
EC cell
Specificity: 1.000
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
153 R → C 0.001887 SNP Missense Mutation UCEC
160 R → C 0.005618 SNP Missense Mutation PAAD
161 R → C 0.002294 SNP Missense Mutation OV
314 R → C 0.001887 SNP Missense Mutation UCEC
381 W → C 0.002020 SNP Missense Mutation PRAD