Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| M0QY43 | MYH14 | Myosin heavy chain 14 | Homo sapiens (Human) | 1002 aa |
Protein Details: M0QY43 (MYH14)
Protein Information
| Accession | M0QY43 |
|---|---|
| Protein Names | Myosin heavy chain 14 |
| Gene Symbol | MYH14 |
| Organism | Homo sapiens (Human) |
| Length | 1002 aa |
| Isoforms | No isoforms |
| Related PMIDs | 31251020 32944167 36430497 31251020 (mass) 32651440 (mass) 36430497 (mass) |
| 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
1-501MAAVTMSVPG11RKAPPRPGPV21PEAAQPFLFT31PRGPSAGGGP41GSGTSPQVEW
51-10051TARRLVWVPS61ELHGFEAAAL71RDEGEEEAEV81ELAESGRRLR91LPRDQIQRMN
101-150101PPKFSKAEDM111AELTCLNEAS121VLHNLRERYY131SGLIYTYSGL141FCVVINPYKQ
151-200151LPIYTEAIVE161MYRGKKRHEV171PPHVYAVTEG181AYRSMLQDRE191DQSILCTGES
201-250201GAGKTENTKK211VIQYLAHVAS221SPKGRKEPGV231PASVSTVSYG241ELERQLLQAN
251-300251PILEAFGNAK261TVKNDNSSRF271GKFIRINFDV281AGYIVGANIE291TYLLEKSRAI
301-350301RQAKDECSFH311IFYQLLGGAG321EQLKADLLLE331PCSHYRFLTN341GPSSSPGQER
351-400351ELFQETLESL361RVLGFSHEEI371ISMLRMVSAV381LQFGNIALKR391ERNTDQATMP
401-450401DNTAAQKLCR411LLGLGVTDFS421RALLTPRIKV431GRDYVQKAQT441KEQADFALEA
451-500451LAKATYERLF461RWLVLRLNRA471LDRSPRQGAS481FLGILDIAGF491EIFQLNSFEQ
501-550501LCINYTNEKL511QQLFNHTMFV521LEQEEYQREG531IPWTFLDFGL541DLQPCIDLIE
551-600551RPANPPGLLA561LLDEECWFPK571ATDKSFVEKV581AQEQGGHPKF591QRPRHLRDQA
601-650601DFSVLHYAGK611VDYKANEWLM621KNMDPLNDNV631AALLHQSTDR641LTAEIWKDVE
651-700651GIVGLEQVSS661LGDGPPGGRP671RRGMFRTVGQ681LYKESLSRLM691ATLSNTNPSF
701-750701VRCIVPNHEK711RAGKLEPRLV721LDQLRCNGVL731EGIRICRQGF741PNRILFQEFR
751-800751QRYEILTPNA761IPKGFMDGKQ771ACEKMIQALE781LDPNLYRVGQ791SKIFFRAGVL
801-850801AQLEEERDLK811VTDIIVSFQA821AARGYLARRA831FQKRQQQQSA841LRVMQRNCAA
851-900851YLKLRHWQWW861RLFTKVKPLL871QVTRQDEVLQ881ARAQELQKVQ891ELQQQSAREV
901-950901GELQGRVAQL911EEERARLAEQ921LRAEAELCAE931AEETRGRLAA941RKQELELVVS
951-1000951ELEARVGEEE961ECSRQMQTEK971KRLQQHIQEL981EAHLEAEEGA991RQKLQLEKVT
1001-10021001TE
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 115 | - | - | - |
GPS-Palm: 0.73
Deep-Palm: 0.85
|
|
| 142 | - | - | - |
Deep-Palm: 0.22
|
|
| 196 | SWISSPALM DBPTM CYSMODDB | Myosin head (motor domain) |
HeLa
(29575903)
|
Unknown
(32651440)
cerebral cortex
(36430497)
|
GPS-Palm: 0.79
Deep-Palm: 0.88
|
| 307 | - | - | - |
Deep-Palm: 0.93
|
|
| 332 | - | - | - |
GPS-Palm: 0.88
Deep-Palm: 0.94
|
|
| 409 | - | - | - |
GPS-Palm: 0.86
Deep-Palm: 0.98
|
|
| 502 | - | - | - |
GPS-Palm: 0.86
Deep-Palm: 0.10
|
|
| 545 | - | - | - |
Deep-Palm: 0.91
|
|
| 566 | - | - | - |
GPS-Palm: 0.82
Deep-Palm: 0.98
|
|
| 703 | - | - | - |
Deep-Palm: 0.88
|
|
| 726 | - | - |
LNCaP
(31251020)
|
GPS-Palm: 0.72
Deep-Palm: 0.97
|
|
| 736 | - | - | - |
GPS-Palm: 0.85
Deep-Palm: 0.94
|
|
| 772 | - | - | - |
GPS-Palm: 0.81
Deep-Palm: 0.84
|
|
| 848 | - | - | - |
GPS-Palm: 0.92
Deep-Palm: 0.32
|
|
| 928 | - | - | - |
Deep-Palm: 0.98
|
|
| 962 | - | - | - |
Deep-Palm: 0.87
|
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): 0.429
3
LNCaP
Specificity: 0.300
3/3 (100.0%)
3
cerebral cortex
Specificity: 0.300
3/3 (100.0%)
1
PC3
Specificity: 0.100
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
3
Cerebral Cortex (Mass)
Specificity: 0.300
3/4 (75.0%)
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.
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 |
|---|---|---|---|---|---|
| 28 | L → Cfs*72 | 0.002976 | DEL | Frame Shift Del | KIRC |
| 54 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 54 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 154 | Y → C | 0.001969 | SNP | Missense Mutation | LGG |
| 167 | R → C | 0.005435 | SNP | Missense Mutation | ESCA |
| 196 | C → C | 0.001887 | SNP | Splice Region | UCEC |
| 267 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 450 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 458 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 520 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 559 | W → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 717 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 820 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 826 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 933 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 956 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 1024 | R → C | 0.004283 | SNP | Missense Mutation | SKCM |
| 1059 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 1237 | G → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1267 | G → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 1273 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1412 | R → C | 0.001969 | SNP | Missense Mutation | LGG |
| 1581 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1581 | R → C | 0.005618 | SNP | Missense Mutation | PAAD |
| 1629 | R → C | 0.002747 | SNP | Missense Mutation | LIHC |
| 1665 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 1665 | R → C | 0.002545 | SNP | Missense Mutation | GBM |
| 1665 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 1749 | R → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 1754 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 1775 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 1794 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 1794 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 1826 | R → C | 0.002294 | SNP | Missense Mutation | OV |
| 1854 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1936 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1947 | R → C | 0.002288 | SNP | Missense Mutation | STAD |