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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
J3KNF8 CYB5B; CYB5M; OMB5 Cytochrome b5 type B (Cytochrome … Homo sapiens (Human) 150 aa

Protein Details: J3KNF8 (CYB5B)

Protein Information
AccessionJ3KNF8
Protein NamesCytochrome b5 type B (Cytochrome b5 outer mitochondrial membrane isoform)
Gene SymbolCYB5B; CYB5M; OMB5
OrganismHomo sapiens (Human)
Length150 aa
IsoformsNo isoforms
Related PMIDs 31251020 32651440 36430497
Database SourcesSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MSGSMATAEA11SGSDGKGQEV21ETSVTYYRLE31EVAKRNSLKE41LWLVIHGRVY
51-10051DVTRFLNEHP61GGEEVLLEQA71GVDASESFED81VGHSSDAREM91LKQYYIGDIH
101-150101PSDLKPESGS111KDPSKNDTCK121SCWAYWILPI131IGAVLLGFLY141RYYTSESKSS
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
119 - - -
Deep-Palm: 0.32
122 - - -
Deep-Palm: 0.83
Score Interpretation:
GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.400
2
LNCaP
Specificity: 0.400
2/2 (100.0%)
2
cerebral cortex
Specificity: 0.400
2/2 (100.0%)
1
Jurkat T cell
Specificity: 0.200
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
Palmitoylation 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
46 Y → C 0.001764 SNP Missense Mutation LUAD