Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| Q5BKV1 | MYH9 | MYH9 protein (Myosin heavy chain … | Homo sapiens (Human) | 218 aa |
Protein Details: Q5BKV1 (MYH9)
Protein Information
| Accession | Q5BKV1 |
|---|---|
| Protein Names | MYH9 protein (Myosin heavy chain 9) |
| Gene Symbol | MYH9 |
| Organism | Homo sapiens (Human) |
| Length | 218 aa |
| Isoforms | No isoforms |
| Related PMIDs | 29575903 31251020 36430497 |
| Database Sources | CysModDBdbPTMSwissPalm |
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
1-501MAQQAADKYL11YVDKNFINNP21LAQADWAAKK31LVWVPSDKSG41FEPASLKEEV
51-10051GEEAIVELVE61NGKKVKVNKD71DIQKMNPPKF81SKVEDMAELT91CLNEASVLHN
101-150101LKERYYSGLI111YTYSGLFCVV121INPYKNLPIY131SEEIVEMYKG141KKRHEMPPHI
151-200151YAITDTAYRS161MMQDREDQSI171LCTGESGAGK181TENTKKVIQY191LAYVASSHKS
201-218201KKDQEAYFKN211RAVRLGVL
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 91 | - | - |
LNCaP
(31251020)
Unknown
(32651440)
|
GPS-Palm: 0.76
Deep-Palm: 0.81
|
|
| 118 | - | - | - |
Deep-Palm: 0.26
|
|
| 172 | SWISSPALM DBPTM CYSMODDB | Myosin head (motor domain) |
HeLa
(29575903)
|
Unknown
(32651440)
cerebral cortex
(36430497)
|
GPS-Palm: 0.79
Deep-Palm: 0.78
|
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
cerebral cortex
Specificity: 0.500
4/4 (100.0%)
3
LNCaP
Specificity: 0.375
3/3 (100.0%)
1
HeLa cell
Specificity: 0.125
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000Palmitoylation 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 |
|---|---|---|---|---|---|
| 91 | C → Y | 0.002506 | SNP | Missense Mutation | COAD |
| 104 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 172 | C → Lfs*4 | 0.001969 | INS | Frame Shift Ins | HNSC |
| 172 | C → Y | 0.001887 | SNP | Missense Mutation | UCEC |
| 240 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 263 | R → C | 0.006944 | SNP | Missense Mutation | TGCT |
| 263 | R → C | 0.002545 | SNP | Missense Mutation | GBM |
| 282 | S → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 393 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 427 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 573 | Y → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 764 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 789 | C → C | 0.001887 | SNP | Silent | UCEC |
| 816 | C → C | 0.002288 | SNP | Silent | STAD |
| 905 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 1114 | S → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 1114 | S → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 1268 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1520 | V → Cfs*137 | 0.002033 | INS | Frame Shift Ins | LUSC |
| 1652 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 1697 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 1697 | R → C | 0.002020 | SNP | Missense Mutation | PRAD |
| 1732 | A → _Q1733insCLLQKIHS | 0.002033 | INS | In Frame Ins | LUSC |
| 1743 | G → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 1838 | R → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 1838 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1912 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |