Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| P04264 | KRT1; KRTA | Keratin, type II cytoskeletal 1 … | Homo sapiens (Human) | 644 aa |
Protein Details: P04264 (KRT1)
Protein Information
| Accession | P04264 |
|---|---|
| Protein Names | Keratin, type II cytoskeletal 1 (67 kDa cytokeratin) (Cytokeratin-1) (CK-1) (Hair alpha protein) (Keratin-1) (K1) (Type-II keratin Kb1) |
| Gene Symbol | KRT1; KRTA |
| Organism | Homo sapiens (Human) |
| Length | 644 aa |
| Isoforms | No isoforms |
| Related PMIDs | 25914232 29733200 31382980 32944167 |
| Database Sources | No database sources |
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.556
Bubble Size: Positive Samples Count
Color Intensity: Positive Ratio
10
HAP1 cells
Specificity: 0.556
10/10 (100.0%)
4
PC3 cells
Specificity: 0.222
4/4 (100.0%)
3
CEMx174 cells
Specificity: 0.167
3/3 (100.0%)
1
U937 cells
Specificity: 0.056
1/1 (100.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (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
T cells
Specificity: 0.000
0/4 (0.0%)
0
293T cells
Specificity: 0.000
0/10 (0.0%)
0
Endothelial cells
Specificity: 0.000
0/2 (0.0%)
0
Prefrontal cortex
Specificity: 0.000
0/1 (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
1-501MSRQFSSRSG11YRSGGGFSSG21SAGIINYQRR31TTSSSTRRSG41GGGGRFSSCG
51-10051GGGGSFGAGG61GFGSRSLVNL71GGSKSISISV81ARGGGRGSGF91GGGYGGGGFG
101-150101GGGFGGGGFG111GGGIGGGGFG121GFGSGGGGFG131GGGFGGGGYG141GGYGPVCPPG
151-200151GIQEVTINQS161LLQPLNVEID171PEIQKVKSRE181REQIKSLNNQ191FASFIDKVRF
201-250201LEQQNQVLQT211KWELLQQVDT221STRTHNLEPY231FESFINNLRR241RVDQLKSDQS
251-300251RLDSELKNMQ261DMVEDYRNKY271EDEINKRTNA281ENEFVTIKKD291VDGAYMTKVD
301-350301LQAKLDNLQQ311EIDFLTALYQ321AELSQMQTQI331SETNVILSMD341NNRSLDLDSI
351-400351IAEVKAQYED361IAQKSKAEAE371SLYQSKYEEL381QITAGRHGDS391VRNSKIEISE
401-450401LNRVIQRLRS411EIDNVKKQIS421NLQQSISDAE431QRGENALKDA441KNKLNDLEDA
451-500451LQQAKEDLAR461LLRDYQELMN471TKLALDLEIA481TYRTLLEGEE491SRMSGECAPN
501-550501VSVSVSTSHT511TISGGGSRGG521GGGGYGSGGS531SYGSGGGSYG541SGGGGGGGRG
551-600551SYGSGGSSYG561SGGGSYGSGG571GGGGHGSYGS581GSSSGGYRGG591SGGGGGGSSG
601-644601GRGSGGGSSG611GSIGGRGSSS621GGVKSSGGSS631SVKFVSTTYS641GVTR
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 49 | 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 |
|---|---|---|---|---|---|
| 16 | G → C | 0.002747 | SNP | Missense Mutation | LIHC |
| 20 | G → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 29 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 29 | R → C | 0.005013 | SNP | Missense Mutation | COAD |
| 29 | R → C | 0.001969 | SNP | Missense Mutation | LGG |
| 89 | G → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 144 | G → C | 0.002747 | SNP | Missense Mutation | LIHC |
| 230 | Y → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 324 | S → C | 0.003460 | SNP | Missense Mutation | CESC |
| 343 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 403 | R → C | 0.003460 | SNP | Missense Mutation | CESC |
| 432 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 463 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 605 | G → C | 0.001969 | SNP | Missense Mutation | HNSC |