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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A8V8TMP3 RPSA 40S ribosomal protein SA Homo sapiens (Human) 194 aa

Protein Details: A0A8V8TMP3 (RPSA)

Protein Information
AccessionA0A8V8TMP3
Protein Names40S ribosomal protein SA
Gene SymbolRPSA
OrganismHomo sapiens (Human)
Length194 aa
IsoformsNo isoforms
Related PMIDs 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
1-501XRFTPGTFTN11QIQAAFREPR21LLVVTDPRAD31HQPLTEASYV41NLPTIALCNT
51-10051DSPLRYVDIA61IPCNNKGAHS71VGLMWWMLAR81EVLRMRGTIS91REHPWEVMPD
101-150101LYFYRDPEEI111EKEEQAAAEK121AVTKEEFQGE131WTAPAPEFTA141TQPEVADWSE
151-194151GVQVPSVPIQ161QFPTDWSAQP171ATEDWSAAPT181AQATEWVGAT191TDWS
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
48 Small ribosomal subunit protein uS2, eukaryotic/archaeal Small ribosomal subunit protein uS2, flavodoxin-like domain superfamily Small ribosomal subunit protein uS2 -
Unknown (32651440)
Deep-Palm: 0.97
63 - - -
Deep-Palm: 0.43
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
3
PC3
Specificity: 1.000
3/3 (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
191 R → C 0.002288 SNP Missense Mutation STAD