Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| A0A0U1RQK9 | ALDH1B1 | aldehyde dehydrogenase (NAD(+)) (EC 1.2.1.3) | Homo sapiens (Human) | 130 aa |
Protein Details: A0A0U1RQK9 (ALDH1B1)
Protein Information
| Accession | A0A0U1RQK9 |
|---|---|
| Protein Names | aldehyde dehydrogenase (NAD(+)) (EC 1.2.1.3) |
| Gene Symbol | ALDH1B1 |
| Organism | Homo sapiens (Human) |
| Length | 130 aa |
| Isoforms | No isoforms |
| Related PMIDs | 19801377 32944167 |
| 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
1-501MLRFLAPRLL11SLQGRTARYS21SAAALPSPIL31NPDIPYNQLF41INNEWQDAVS
51-10051KKTFPTVNPT61TGEVIGHVAE71GDRADVDRAV81KAAREAFRLG91SPWRRMDASE
101-130101RGRLLNRLAD111LVERDRVYLA121SLETLDNGKP
Palmitoylation Sites Details
No known palmitoylation sites
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.667
2
PC3
Specificity: 0.667
2/2 (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.
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 |
|---|---|---|---|---|---|
| 19 | Y → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 88 | R → C | 0.003559 | SNP | Missense Mutation | KIRP |
| 107 | R → C | 0.001969 | SNP | Missense Mutation | LGG |
| 418 | F → C | 0.001969 | SNP | Missense Mutation | LGG |