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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A087WT55 DCP1A 5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase (EC 3.6.1.62) Homo sapiens (Human) 260 aa

Protein Details: A0A087WT55 (DCP1A)

Protein Information
AccessionA0A087WT55
Protein Names5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase (EC 3.6.1.62)
Gene SymbolDCP1A
OrganismHomo sapiens (Human)
Length260 aa
IsoformsNo isoforms
Related PMIDs 31382980
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MEALSRAGQE11MSLAALKQHD21PYITSIADLT31GQEKTDIEGT41LFVYRRSASP
51-10051YHGFTIVNRL61NMHNLVEPVN71KDLEFQLHEP81FLLYRNASLS91IYSIWFYDKN
101-150101DCHRIAKLMA111DVVEEETRRS121QQAARDKQSP131SQANGCSDHR141PIDILEMLSR
151-200151AKDEYERNQM161GDSNISSPGL171QPSTQLSNLG181STETLEEMPS191GSQDKSAPSG
201-250201HKHLTVEELF211GTSLPKEQPA221VVGLDSEEME231RLPGDASQKE241PNSFLPFPFE
251-260251QLGGAPQSET
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
102 - - -
Deep-Palm: 0.12
136 - - -
Deep-Palm: 0.62
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
U937 cell
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.
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
31 G → C 0.002506 SNP Missense Mutation COAD
39 C → C 0.001887 SNP Silent UCEC
117 R → C 0.002506 SNP Missense Mutation COAD