Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| A0A2R8Y4R4 | ATP2B2 | ATPase plasma membrane Ca2+ transporting … | Homo sapiens (Human) | 996 aa |
Protein Details: A0A2R8Y4R4 (ATP2B2)
Protein Information
| Accession | A0A2R8Y4R4 |
|---|---|
| Protein Names | ATPase plasma membrane Ca2+ transporting 2 |
| Gene Symbol | ATP2B2 |
| Organism | Homo sapiens (Human) |
| Length | 996 aa |
| Isoforms | No isoforms |
| Related PMIDs | 26876311 |
| Database Sources | No database sources |
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
Bubble Size: Positive Samples Count
Color Intensity: Positive Ratio
1
Prefrontal cortex
Specificity: 1.000
1/1 (100.0%)
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
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (0.0%)
0
PC3 cells
Specificity: 0.000
0/4 (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
Cerebral cortex
Specificity: 0.000
0/4 (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
1-501DESSLTGESD11QVRKSVDKDP21MLLSGTHVME31GSGRMLVTAV41GVNSQTGIIF
51-10051TLLGAGGEEE61EKKDKKAADG71AAASNAADSA81NASLVNGKMQ91DGNVDASQSK
101-150101AKQQDGAAAM111EMQPLKSAEG121GDADDRKKAS131MHKKEKSVLQ141GKLTKLAVQI
151-200151GKAGLVMSAI161TVIILVLYFT171VDTFVVNKKP181WLPECTPVYV191QYFVKFFIIG
201-250201VTVLVVAVPE211GLPLAVTISL221AYSVKKMMKD231NNLVRHLDAC241ETMGNATAIC
251-300251SDKTGTLTTN261RMTVVQAYVG271DVHYKEIPDP281SSINTKTMEL291LINAIAINSA
301-350301YTTKILPPEK311EGALPRQVGN321KTECGLLGFV331LDLKQDYEPV341RSQMPEEKLY
351-400351KVYTFNSVRK361SMSTVIKLPD371ESFRMYSKGA381SEIVLKKCCK391ILNGAGEPRV
401-450401FRPRDRDEMV411KKVIEPMACD421GLRTICVAYR431DFPSSPEPDW441DNENDILNEL
451-500451TCICVVGIED461PVRPEVPEAI471RKCQRAGITV481RMVTGDNINT491ARAIAIKCGI
501-550501IHPGEDFLCL511EGKEFNRRIR521NEKGEIEQER531IDKIWPKLRV541LARSSPTDKH
551-600551TLVKGIIDST561HTEQRQVVAV571TGDGTNDGPA581LKKADVGFAM591GIAGTDVAKE
601-650601ASDIILTDDN611FSSIVKAVMW621GRNVYDSISK631FLQFQLTVNV641VAVIVAFTGA
651-700651CITQDSPLKA661VQMLWVNLIM671DTFASLALAT681EPPTETLLLR691KPYGRNKPLI
701-750701SRTMMKNILG711HAVYQLALIF721TLLFVGEKMF731QIDSGRNAPL741HSPPSEHYTI
751-800751IFNTFVMMQL761FNEINARKIH771GERNVFDGIF781RNPIFCTIVL791GTFAIQIVIV
801-850801QFGGKPFSCS811PLQLDQWMWC821IFIGLGELVW831GQVIATIPTS841RLKFLKEAGR
851-900851LTQKEEIPEE861ELNEDVEEID871HAERELRRGQ881ILWFRGLNRI891QTQIRVVKAF
901-950901RSSLYEGLEK911PESRTSIHNF921MAHPEFRIED931SQPHIPLIDD941TDLEEDAALK
951-996951QNSSPPSSLN961KNNSAIDSGI971NLTTDTSKSA981TSSSPGSPIH991SLETSL
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 250 | Prediction (Medium) | - | - |
| 324 | Prediction (Medium) | - | - |
| 388 | Prediction (Low) | - | - |
| 389 | Prediction (Medium) | - | - |
| 419 | Prediction (Medium) | - | - |
| 426 | Prediction (Low) | - | - |
| 473 | Prediction (Medium) | - | - |
| 498 | Prediction (Medium) | - | - |
| 509 | Prediction (Medium) | - | - |
| 651 | Prediction (Medium) | - | - |
| 809 | Prediction (Medium) | - | - |
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 |
|---|---|---|---|---|---|
| 32 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 32 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 59 | R → C | 0.002294 | SNP | Missense Mutation | OV |
| 86 | F → C | 0.007299 | SNP | Missense Mutation | READ |
| 151 | W → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 185 | R → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 249 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 249 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 432 | C → S | 0.006944 | SNP | Missense Mutation | TGCT |
| 491 | G → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 497 | C → S | 0.001764 | SNP | Missense Mutation | LUAD |
| 559 | G → C | 0.002288 | SNP | Missense Mutation | STAD |
| 588 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 597 | Y → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 606 | R → C | 0.001969 | SNP | Missense Mutation | HNSC |
| 606 | R → C | 0.002020 | SNP | Missense Mutation | PRAD |
| 606 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 621 | R → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 621 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 651 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 666 | C → C | 0.001887 | SNP | Silent | UCEC |
| 673 | C → C | 0.001887 | SNP | Silent | UCEC |
| 677 | R → C | 0.005435 | SNP | Missense Mutation | ESCA |
| 699 | C → C | 0.001887 | SNP | Silent | UCEC |
| 869 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1014 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1020 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1055 | S → C | 0.002747 | SNP | Missense Mutation | LIHC |
| 1067 | C → C | 0.003460 | SNP | Silent | CESC |
| 1142 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 1178 | S → C | 0.002294 | SNP | Missense Mutation | OV |
| 1211 | S → C | 0.001764 | SNP | Missense Mutation | LUAD |