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UniProt ID Gene Symbol Protein Name Organism Length Action
M0QZW2 CD70 CD70 molecule Homo sapiens (Human) 65 aa

Protein Details: M0QZW2 (CD70)

Protein Information
AccessionM0QZW2
Protein NamesCD70 molecule
Gene SymbolCD70
OrganismHomo sapiens (Human)
Length65 aa
IsoformsNo isoforms
Related PMIDs 32944167
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MPEEGSGCSV11RRRPYGCVLR21AALVPLVAGL31VICLVVCIQR41FAQAQQQLPL
51-6551ESLGWDVAEL61QLNHT
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
8 SWISSPALM DBPTM CYSMODDB -
HeLa (29575903)
-
GPS-Palm: 0.91
Deep-Palm: 0.06
17 SWISSPALM DBPTM CYSMODDB -
HeLa (29575903)
-
GPS-Palm: 0.81
Deep-Palm: 0.98
33 CD70 antigen - -
GPS-Palm: 0.87
Deep-Palm: 0.98
37 CD70 antigen - -
GPS-Palm: 0.88
Deep-Palm: 0.98
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
97 R → C 0.001887 SNP Missense Mutation UCEC
144 R → C 0.001887 SNP Missense Mutation UCEC
157 R → C 0.006993 SNP Missense Mutation LAML
192 R → C 0.005013 SNP Missense Mutation COAD