Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| B7Z645 | SYNCRIP; hCG_401112 | Heterogeneous nuclear ribonucleoprotein Q (Synaptotagmin … | Homo sapiens (Human) | 464 aa |
Protein Details: B7Z645 (SYNCRIP)
Protein Information
| Accession | B7Z645 |
|---|---|
| Protein Names | Heterogeneous nuclear ribonucleoprotein Q (Synaptotagmin binding cytoplasmic RNA interacting protein) (Synaptotagmin binding, cytoplasmic RNA interacting protein, isoform CRA_b) |
| Gene Symbol | SYNCRIP; hCG_401112 |
| Organism | Homo sapiens (Human) |
| Length | 464 aa |
| Isoforms | No isoforms |
| Related PMIDs | 29575903 32944167 36430497 |
| Database Sources | CysModDB dbPTM SwissPalm |
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.600
Bubble Size: Positive Samples Count
Color Intensity: Positive Ratio
3
PC3 cells
Specificity: 0.600
3/4 (75.0%)
1
HeLa cells
Specificity: 0.200
1/1 (100.0%)
1
Cerebral cortex
Specificity: 0.200
1/4 (25.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (0.0%)
0
T cells
Specificity: 0.000
0/4 (0.0%)
0
HAP1 cells
Specificity: 0.000
0/10 (0.0%)
0
293T cells
Specificity: 0.000
0/10 (0.0%)
0
CEMx174 cells
Specificity: 0.000
0/3 (0.0%)
0
Endothelial cells
Specificity: 0.000
0/2 (0.0%)
0
Prefrontal cortex
Specificity: 0.000
0/1 (0.0%)
0
Liver membrane
Specificity: 0.000
0/1 (0.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID).
The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
Bars are grouped by tissue/cell line for easy comparison.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MKTYRQREKQ11GTKVADSSKG21PDEAKIKALL31ERTGYTLDVT41TGQRKYGGPP
51-10051PDSVYSGQQP61SVGTEIFVGK71IPRDLFEDEL81VPLFEKAGPI91WDLRLMMDPL
101-150101TGLNRGYAFV111TFCTKEAAQE121AVKLYNNHEI131RSGKHIGVCI141SVANNRLFVG
151-200151SIPKSKTKEQ161ILEEFSKVTE171GLTDVILYHQ181PDDKKKNRGF191CFLEYEDHKT
201-250201AAQARRRLMS211GKVKVWGNVG221TVEWADPIED231PDPEVMAKVK241VLFVRNLANT
251-300251VTEEILEKAF261SQFGKLERVK271KLKDYAFIHF281DERDGAVKAM291EEMNGKDLEG
301-350301ENIEIVFAKP311PDQKRKERKA321QRQAAKNQMY331DDYYYYGPPH341MPPPTRGRGR
351-400351GGRGGYGYPP361DYYGYEDYYD371YYGYDYHNYR381GGYEDPYYGY391EDFQVGARGR
401-450401GGRGARGAAP411SRGRGAAPPR421GRAGYSQRGG431PGSARGVRGA441RGGAQQQRGR
451-464451GQGKGVEAGP461DLLQ
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 113 | CYSMODDB SWISSPALM DBPTM Prediction (Medium) | RNA recognition motif | - |
| 139 | Prediction (Medium) | - | - |
| 191 | CYSMODDB SWISSPALM DBPTM Prediction (Low) | - | - |
Conservation Scores
PhyloP
PhastCons
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 |
|---|---|---|---|---|---|
| 55 | S → delinsRRCI | 0.002033 | INS | In Frame Ins | LUSC |
| 229 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 229 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 229 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 276 | Y → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 304 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 358 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 448 | R → C | 0.003774 | SNP | Missense Mutation | UCEC |
| 460 | Y → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 469 | Y → C | 0.002294 | SNP | Missense Mutation | OV |
| 548 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 548 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |