Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| P50281 | MMP14 | Matrix metalloproteinase-14 (MMP-14) (EC 3.4.24.80) … | Homo sapiens (Human) | 582 aa |
Protein Details: P50281 (MMP14)
Protein Information
| Accession | P50281 |
|---|---|
| Protein Names | Matrix metalloproteinase-14 (MMP-14) (EC 3.4.24.80) (MMP-X1) (Membrane-type matrix metalloproteinase 1) (MT-MMP 1) (MTMMP1) (Membrane-type-1 matrix metalloproteinase) (MT1-MMP) (MT1MMP) |
| Gene Symbol | MMP14 |
| Organism | Homo sapiens (Human) |
| Length | 582 aa |
| Isoforms | No isoforms |
| Related PMIDs | 19801377 22496122 24357059 |
| Database Sources | dbPTMSwissPalm |
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
1-501MSPAPRPPRC11LLLPLLTLGT21ALASLGSAQS31SSFSPEAWLQ41QYGYLPPGDL
51-10051RTHTQRSPQS61LSAAIAAMQK71FYGLQVTGKA81DADTMKAMRR91PRCGVPDKFG
101-150101AEIKANVRRK111RYAIQGLKWQ121HNEITFCIQN131YTPKVGEYAT141YEAIRKAFRV
151-200151WESATPLRFR161EVPYAYIREG171HEKQADIMIF181FAEGFHGDST191PFDGEGGFLA
201-250201HAYFPGPNIG211GDTHFDSAEP221WTVRNEDLNG231NDIFLVAVHE241LGHALGLEHS
251-300251SDPSAIMAPF261YQWMDTENFV271LPDDDRRGIQ281QLYGGESGFP291TKMPPQPRTT
301-350301SRPSVPDKPK311NPTYGPNICD321GNFDTVAMLR331GEMFVFKERW341FWRVRNNQVM
351-400351DGYPMPIGQF361WRGLPASINT371AYERKDGKFV381FFKGDKHWVF391DEASLEPGYP
401-450401KHIKELGRGL411PTDKIDAALF421WMPNGKTYFF431RGNKYYRFNE441ELRAVDSEYP
451-500451KNIKVWEGIP461ESPRGSFMGS471DEVFTYFYKG481NKYWKFNNQK491LKVEPGYPKS
501-550501ALRDWMGCPS511GGRPDEGTEE521ETEVIIIEVD531EEGGGAVSAA541AVVLPVLLLL
551-582551LVLAVGLAVF561FFRRHGTPRR571LLYCQRSLLD581KV
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 10 | - | - | - |
GPS-Palm: 0.71
Deep-Palm: 0.92
|
|
| 93 | - | - | - |
GPS-Palm: 0.87
Deep-Palm: 0.93
|
|
| 127 | - | - | - |
Deep-Palm: 0.08
|
|
| 319 | - | - | - |
Deep-Palm: 0.22
|
|
| 508 | - | - | - |
GPS-Palm: 0.82
Deep-Palm: 0.88
|
|
| 574 | DBPTM SWISSPALM | Domain of unknown function (DUF3377) | - | - |
GPS-Palm: 0.95
Deep-Palm: 0.14
|
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): 0.333
1
EC cell
Specificity: 0.333
1/1 (100.0%)
1
HUVECs
Specificity: 0.333
1/1 (100.0%)
1
DU145 cell
Specificity: 0.333
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 |
|---|---|---|---|---|---|
| 10 | C → R | 0.002545 | SNP | Missense Mutation | GBM |
| 145 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 149 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 160 | R → C | 0.002545 | SNP | Missense Mutation | GBM |
| 206 | G → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 283 | Y → C | 0.002288 | SNP | Missense Mutation | STAD |
| 339 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 431 | R → C | 0.007299 | SNP | Missense Mutation | READ |
| 431 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 478 | Y → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 576 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |