Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| Q9Y6G5 | COMMD10 | COMM domain-containing protein 10 | Homo sapiens (Human) | 202 aa |
Protein Details: Q9Y6G5 (COMMD10)
Protein Information
| Accession | Q9Y6G5 |
|---|---|
| Protein Names | COMM domain-containing protein 10 |
| Gene Symbol | COMMD10 |
| Organism | Homo sapiens (Human) |
| Length | 202 aa |
| Isoforms | No isoforms |
| Related PMIDs | No related PMIDs |
| Database Sources | SwissPalm |
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
Experimental Database High Prediction Non-palmitylated Cys
1-501MAVPAALILR11ESPSMKKAVS21LINAIDTGRF31PRLLTRILQK41LHLKAESSFS
51-10051EEEEEKLQAA61FSLEKQDLHL71VLETISFILE81QAVYHNVKPA91ALQQQLENIH
101-150101LRQDKAEAFV111NTWSSMGQET121VEKFRQRILA131PCKLETVGWQ141LNLQMAHSAQ
151-200151AKLKSPQAVL161QLGVNNEDSK171SLEKVLVEFS181HKELFDFYNK191LETIQAQLDS
201-202201LT
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 132 | - |
HeLa
(37611173)
| - |
GPS-Palm: 0.89
Deep-Palm: 0.94
|
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)
• 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)
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
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 |
|---|---|---|---|---|---|
| 124 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 139 | W → C | 0.001764 | SNP | Missense Mutation | LUAD |