Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
B0FYL2 ATP2A2 ATPase CA++ transporting cardiac muscle … Homo sapiens (Human) 33 aa

Protein Details: B0FYL2 (ATP2A2)

Protein Information
AccessionB0FYL2
Protein NamesATPase CA++ transporting cardiac muscle slow twitch 2
Gene SymbolATP2A2
OrganismHomo sapiens (Human)
Length33 aa
IsoformsNo isoforms
Related PMIDs 26876311 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
1-331LPAEEGKTLL11ELVIEQFEDL21LVRILLLEAC31ISF
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
30 - - -
GPS-Palm: 0.97
Deep-Palm: 0.04
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): 0.800
4
PC3
Specificity: 0.800
4/4 (100.0%)
1
frontal cortex
Specificity: 0.200
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.
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
256 F → C 0.001887 SNP Missense Mutation UCEC
349 C → Kfs*17 0.001887 DEL Frame Shift Del UCEC
407 Y → C 0.002033 SNP Missense Mutation THCA
434 Y → C 0.001887 SNP Missense Mutation UCEC
487 F → C 0.001887 SNP Missense Mutation UCEC
730 S → C 0.001969 SNP Missense Mutation HNSC
835 R → C 0.002141 SNP Missense Mutation SKCM
901 S → C 0.002427 SNP Missense Mutation BLCA
909 C → C 0.001969 SNP Silent LGG
914 S → C 0.002506 SNP Missense Mutation COAD
1027 I → Cfs*4 0.002506 INS Frame Shift Ins COAD
1028 W → C 0.001969 SNP Missense Mutation HNSC