Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
C9J6Y3 SLC26A6 Solute carrier family 26 member … Homo sapiens (Human) 169 aa

Protein Details: C9J6Y3 (SLC26A6)

Protein Information
AccessionC9J6Y3
Protein NamesSolute carrier family 26 member 6
Gene SymbolSLC26A6
OrganismHomo sapiens (Human)
Length169 aa
IsoformsNo isoforms
Related PMIDs 31251020 32944167
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MGLADASGPR11DTQALLSATQ21AMDLRRRDYH31MERPLLNQEH41LEELGRWGSA
51-10051PRTHQWRTWL61QCSRARAYAL71LLQHLPVLVW81LPRYPVRDWL91LGDLLSGLSV
101-150101AIMQLPQGLA111YALLAGLPPV121FGLYSSFYPV131FIYFLFGTSR141HISVATPGPL
151-169151PLLTAPGRPT161GGAGPDPLR
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
62 SWISSPALM DBPTM CYSMODDB -
HeLa (29575903)
-
GPS-Palm: 0.76
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): 0.500
4
LNCaP
Specificity: 0.500
4/4 (100.0%)
4
PC3
Specificity: 0.500
4/4 (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
87 R → C 0.001764 SNP Missense Mutation LUAD
97 G → C 0.001887 SNP Missense Mutation UCEC
531 Y → C 0.002506 SNP Missense Mutation COAD
544 R → C 0.002033 SNP Missense Mutation LUSC
544 R → C 0.002141 SNP Missense Mutation SKCM
683 T → _V684insHYSECACEGGF 0.005435 INS In Frame Ins ESCA
400* C → ? 0.002288 SNP Nonsense Mutation STAD