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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
F8VWB0 SLC11A2 Solute carrier family 11 member … Homo sapiens (Human) 149 aa

Protein Details: F8VWB0 (SLC11A2)

Protein Information
AccessionF8VWB0
Protein NamesSolute carrier family 11 member 2
Gene SymbolSLC11A2
OrganismHomo sapiens (Human)
Length149 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
1-501MVLGPEQKMS11DDSVSGDHGE21SASLGNINPA31YSNPSLSQSP41GDSEEYFATY
51-10051FNEKISIPEE61EYSCFSFRKL71WAFTGPGFLM81SIAYLDPGNI91ESDLQSGAVA
101-149101GFKLLWILLL111ATLVGLLLQR121LAARLGVVTG131LHLAEVCHRQ141YPKVPRVIL
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
64 SWISSPALM DBPTM CYSMODDB -
HeLa (29575903)
-
GPS-Palm: 0.88
Deep-Palm: 0.68
137 - -
LNCaP (31251020)
GPS-Palm: 0.81
Deep-Palm: 0.97
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
LNCaP
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
176 S → C 0.003460 SNP Missense Mutation CESC
245 C → W 0.001887 SNP Missense Mutation UCEC
408 R → C 0.002506 SNP Missense Mutation COAD
489 S → C 0.001014 SNP Missense Mutation BRCA
544 C → C 0.001887 SNP Splice Region UCEC