Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A0C4DGB6 ALB Albumin Homo sapiens (Human) 604 aa

Protein Details: A0A0C4DGB6 (ALB)

Protein Information
Accession A0A0C4DGB6
Protein Names Albumin
Gene Symbol ALB
Organism Homo sapiens (Human)
Length 604 aa
Isoforms No isoforms
Related PMIDs 21076176
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
4
Jurkat T cells
Specificity: 1.000
4/25 (16.0%)
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
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
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
1-501MKWVTFISLL11FLFSSAYSRG21VFRRDAHKSE31VAHRFKDLGE41ENFKALVLIA
51-10051FAQYLQQCPF61EDHVKLVNEV71TEFAKTCVAD81ESAENCDKSL91HTLFGDKLCT
101-150101VATLRETYGE111MADCCAKQEP121ERNECFLQHK131DDNPNLPRLV141RPEVDVMCTA
151-200151FHDNEETFLK161KYLYEIARRH171PYFYAPELLF181FAKRYKAAFT191ECCQAADKAA
201-250201CLLPKLDELR211DEGKASSAKQ221RLKCASLQKF231GERAFKAWAV241ARLSQRFPKA
251-300251EFAEVSKLVT261DLTKVHTECC271HGDLLECADD281RADLAKYICE291NQDSISSKLK
301-350301ECCEKPLLEK311SHCIAEVEND321EMPADLPSLA331ADFVESKDVC341KNYAEAKDVF
351-400351LGMFLYEYAR361RHPDYSVVLL371LRLAKTYETT381LEKCCAAADP391HECYAKVFDE
401-450401FKPLVEEPQN411LIKQNCELFE421QLGEYKFQNA431LLVRYTKKVP441QVSTPTLVEV
451-500451SRNLGKVGSK461CCKHPEAKRM471PCAEDYLSVV481LNQLCVLHEK491TPVSDRVTKC
501-550501CTESLVNRRP511CFSALEVDET521YVPKEFNAET531FTFHADICTL541SEKERQIKKQ
551-600551TALVELVKHK561PKATKEQLKA571VMDDFAAFVE581KCCKADDKET591CFAEEPTMRI
601-604601RERK
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
99 Prediction (Medium) - -
192 Prediction (Medium) - -
193 Prediction (Medium) - -
201 Prediction (Medium) - -
224 Prediction (High) - -
289 Prediction (Low) - -
303 Prediction (Medium) - -
416 Prediction (Medium) - -
461 Prediction (Medium) - -
462 Prediction (Medium) - -
485 Prediction (Low) - -
500 Prediction (Medium) - -
501 Prediction (Medium) - -
538 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
17 Y → C 0.002747 SNP Missense Mutation LIHC
23 R → C 0.002141 SNP Missense Mutation SKCM
114 C → Sfs*9 0.002747 INS Frame Shift Ins LIHC
148 C → R 0.001887 SNP Missense Mutation UCEC
193 C → C 0.007299 SNP Silent READ
224 C → Ifs*22 0.002747 DEL Frame Shift Del LIHC
302 C → F 0.002747 SNP Missense Mutation LIHC
307 L → Cfs*23 0.019608 DEL Frame Shift Del CHOL
313 C → C 0.001887 SNP Silent UCEC
355 L → Cfs*17 0.002288 DEL Frame Shift Del STAD
358 Y → C 0.002747 SNP Missense Mutation LIHC
434 R → C 0.002288 SNP Missense Mutation STAD
434 R → C 0.002033 SNP Missense Mutation LUSC
434 R → C 0.004283 SNP Missense Mutation SKCM
434 R → C 0.003774 SNP Missense Mutation UCEC
448 V → Cfs*16 0.002747 INS Frame Shift Ins LIHC
591 C → Y 0.002294 SNP Missense Mutation OV
125* C → ? 0.001887 SNP Nonsense Mutation UCEC