Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| P13645 | KRT10 | Keratin, type I cytoskeletal 10 … | Homo sapiens (Human) | 584 aa |
Protein Details: P13645 (KRT10)
Protein Information
| Accession | P13645 |
|---|---|
| Protein Names | Keratin, type I cytoskeletal 10 (Cytokeratin-10) (CK-10) (Keratin-10) (K10) |
| Gene Symbol | KRT10 |
| Organism | Homo sapiens (Human) |
| Length | 584 aa |
| Isoforms | No isoforms |
| Related PMIDs | 25914232 31382980 32944167 31251020 (mass) 32651440 (mass) 36430497 (mass) |
| 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
1-501MSVRYSSSKH11YSSSRSGGGG21GGGGCGGGGG31VSSLRISSSK41GSLGGGFSSG
51-10051GFSGGSFSRG61SSGGGCFGGS71SGGYGGLGGF81GGGSFRGSYG91SSSFGGSYGG
101-150101IFGGGSFGGG111SFGGGSFGGG121GFGGGGFGGG131FGGGFGGDGG141LLSGNEKVTM
151-200151QNLNDRLASY161LDKVRALEES171NYELEGKIKE181WYEKHGNSHQ191GEPRDYSKYY
201-250201KTIDDLKNQI211LNLTTDNANI221LLQIDNARLA231ADDFRLKYEN241EVALRQSVEA
251-300251DINGLRRVLD261ELTLTKADLE271MQIESLTEEL281AYLKKNHEEE291MKDLRNVSTG
301-350301DVNVEMNAAP311GVDLTQLLNN321MRSQYEQLAE331QNRKDAEAWF341NEKSKELTTE
351-400351IDNNIEQISS361YKSEITELRR371NVQALEIELQ381SQLALKQSLE391ASLAETEGRY
401-450401CVQLSQIQAQ411ISALEEQLQQ421IRAETECQNT431EYQQLLDIKI441RLENEIQTYR
451-500451SLLEGEGSSG461GGGRGGGSFG471GGYGGGSSGG481GSSGGGHGGG491HGGSSGGGYG
501-550501GGSSGGGSSG511GGYGGGSSSG521GHGGSSSGGY531GGGSSGGGGG541GYGGGSSGGG
551-584551SSSGGGYGGG561SSSGGHKSSS571SGSVGESSSK581GPRY
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 25 | - | - |
Brain
(35358180)
Brain
(31311849)
Unknown
(32651440)
cerebral cortex
(36430497)
|
GPS-Palm: 0.83
Deep-Palm: 0.96
|
|
| 66 | - | - |
Brain
(35358180)
Brain
(31311849)
Unknown
(32651440)
cerebral cortex
(36430497)
|
GPS-Palm: 0.68
Deep-Palm: 0.94
|
|
| 401 | - | - |
Liver
(34884899)
Brain
(35358180)
Unknown
(32651440)
|
Deep-Palm: 0.97
|
|
| 427 | - | - |
Brain
(35358180)
Brain
(31311849)
Unknown
(32651440)
cerebral cortex
(36430497)
|
Deep-Palm: 0.86
|
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)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.500
4
PC3
Specificity: 0.333
4/4 (100.0%)
3
CEM 174 cell
Specificity: 0.250
3/3 (100.0%)
1
U937 cell
Specificity: 0.083
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
4
Cerebral Cortex (Mass)
Specificity: 0.333
4/4 (100.0%)
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.
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 |
|---|---|---|---|---|---|
| 15 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 44 | G → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 56 | S → C | 0.003460 | SNP | Missense Mutation | CESC |
| 83 | G → C | 0.002545 | SNP | Missense Mutation | GBM |
| 86 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 94 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 200 | Y → C | 0.002506 | SNP | Missense Mutation | COAD |
| 256 | R → C | 0.005435 | SNP | Missense Mutation | ESCA |
| 399 | R → C | 0.002020 | SNP | Missense Mutation | PRAD |
| 562 | S → C | 0.002427 | SNP | Missense Mutation | BLCA |
| 584 | Y → C | 0.002033 | SNP | Missense Mutation | LUSC |