Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
H0YC03 TOP1MT DNA topoisomerase I mitochondrial Homo sapiens (Human) 123 aa

Protein Details: H0YC03 (TOP1MT)

Protein Information
AccessionH0YC03
Protein NamesDNA topoisomerase I mitochondrial
Gene SymbolTOP1MT
OrganismHomo sapiens (Human)
Length123 aa
IsoformsNo isoforms
Related PMIDs 31251020
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MLRLRAALTL11LGEVPRRPAS21RGVPGSRRTQ31KGSGARWEKE41KHEDGVKWRQ
51-10051LEHKGPYFAP61PYEPLPDGVR71FFYEGRPVRL81SVAAEEVATF91YGRMLDHEYT
101-123101TKEVFRKNFF111NDWRKVLCQT121HML
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
118 SWISSPALM DBPTM CYSMODDB Eukaryotic DNA topoisomerase I DNA binding fragment - -
Deep-Palm: 0.03
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
2
LNCaP
Specificity: 1.000
2/2 (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
200 R → C 0.002288 SNP Missense Mutation STAD
200 R → C 0.002506 SNP Missense Mutation COAD
294 R → C 0.001887 SNP Missense Mutation UCEC
370 C → Y 0.001887 SNP Missense Mutation UCEC
443 R → C 0.002506 SNP Missense Mutation COAD