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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
D6RIZ7 CCT5 Chaperonin containing TCP1 subunit 5 Homo sapiens (Human) 44 aa

Protein Details: D6RIZ7 (CCT5)

Protein Information
Accession D6RIZ7
Protein Names Chaperonin containing TCP1 subunit 5
Gene Symbol CCT5
Organism Homo sapiens (Human)
Length 44 aa
Isoforms No isoforms
Related PMIDs 19137006 22496122 31251020 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.686
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
24
LNCaP cells
Specificity: 0.686
24/46 (52.2%)
6
Jurkat T cells
Specificity: 0.171
6/25 (24.0%)
4
PC3 cells
Specificity: 0.114
4/4 (100.0%)
1
Endothelial cells
Specificity: 0.029
1/2 (50.0%)
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
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
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
1-441MASMGTLAFD11EYGRPFLIIK21DQDRKSRLMG31LEALKGQQLS41PTDG
Palmitoylation Sites Details

No known palmitoylation sites

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
12 Y → C 0.001887 SNP Missense Mutation UCEC
386 F → C 0.001887 SNP Missense Mutation UCEC
429 C → C 0.027027 SNP Silent DLBC
534 R → C 0.003774 SNP Missense Mutation UCEC