Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| E7ESH4 | HSPD1 | 60 kDa heat shock protein, … | Homo sapiens (Human) | 231 aa |
Protein Details: E7ESH4 (HSPD1)
Protein Information
| Accession | E7ESH4 |
|---|---|
| Protein Names | 60 kDa heat shock protein, mitochondrial (EC 5.6.1.7) (60 kDa chaperonin) (Chaperonin 60) (Heat shock protein 60) |
| Gene Symbol | HSPD1 |
| Organism | Homo sapiens (Human) |
| Length | 231 aa |
| Isoforms | No isoforms |
| Related PMIDs | 21076176 22496122 31251020 36430497 |
| Database Sources | No database sources |
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
1-501MLRLPTVFRQ11MRPVSRVLAP21HLTRAYAKDV31KFGADARALM41LQGVDLLADA
51-10051VAVTMGPKGR61TVIIEQSWGS71PKVTKDGVTV81AKSIDLKDKY91KNIGAKLVQD
101-150101VANNTNEEAG111DGTTTATVLA121RSIAKEGFEK131ISKGANPVEI141RRGVMLAVDA
151-200151VIAELKKQSK161PVTTPEEIAQ171VATISANGDK181EIGNIISDAM191KKVGRKGVIT
201-231201DGKTLNDELE211IIEGMKFDRG221YISPYFINTS231K
Palmitoylation Sites Details
No known palmitoylation sites
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.444
4
cerebral cortex
Specificity: 0.444
4/4 (100.0%)
3
LNCaP
Specificity: 0.333
3/3 (100.0%)
1
Jurkat T cell
Specificity: 0.111
1/1 (100.0%)
1
EC cell
Specificity: 0.111
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.
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 |
|---|---|---|---|---|---|
| 362 | G → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 370 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 370 | R → C | 0.002020 | SNP | Missense Mutation | PRAD |
| 370 | R → C | 0.003774 | SNP | Missense Mutation | UCEC |