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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A0S2Z3H0 ATP2A2 ATPase Ca++ transporting cardiac muscle … Homo sapiens (Human) 63 aa

Protein Details: A0A0S2Z3H0 (ATP2A2)

Protein Information
AccessionA0A0S2Z3H0
Protein NamesATPase Ca++ transporting cardiac muscle slow twitch 2 isoform 3
Gene SymbolATP2A2
OrganismHomo sapiens (Human)
Length63 aa
IsoformsNo isoforms
Related PMIDs 26876311 32944167 36430497
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MENAHTKTVE11EVLGHFGVNE21STGLSLEQVK31KLKERWGSFP41LLGYWLLRRR
51-6351CYRGCCCMVV61HCC
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
51 - - -
GPS-Palm: 0.88
Deep-Palm: 0.04
55 - - -
GPS-Palm: 0.96
Deep-Palm: 0.02
56 - - -
GPS-Palm: 0.94
Deep-Palm: 0.02
57 - - -
GPS-Palm: 0.96
Deep-Palm: 0.02
62 - - -
GPS-Palm: 0.97
Deep-Palm: 0.02
63 - - -
GPS-Palm: 0.97
Deep-Palm: 0.01
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): 0.444
4
PC3
Specificity: 0.444
4/4 (100.0%)
4
cerebral cortex
Specificity: 0.444
4/4 (100.0%)
1
frontal cortex
Specificity: 0.111
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