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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q99732 LITAF Lipopolysaccharide-induced tumor necrosis factor-alpha factor … Homo sapiens (Human) 161 aa

Protein Details: Q99732 (LITAF)

Protein Information
AccessionQ99732
Protein NamesLipopolysaccharide-induced tumor necrosis factor-alpha factor (LPS-induced TNF-alpha factor) (Small integral membrane protein of lysosome/late endosome) (p53-induced gene 7 protein)
Gene SymbolLITAF
OrganismHomo sapiens (Human)
Length161 aa
IsoformsNo isoforms
Related PMIDs No related PMIDs
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MSVPGPYQAA11TGPSSAPSAP21PSYEETVAVN31SYYPTPPAPM41PGPTTGLVTG
51-10051PDGKGMNPPS61YYTQPAPIPN71NNPITVQTVY81VQHPITFLDR91PIQMCCPSCN
101-150101KMIVSQLSYN111AGALTWLSCG121SLCLLGCIAG131CCFIPFCVDA141LQDVDHYCPN
151-161151CRALLGTYKR161L
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
95 - - -
GPS-Palm: 0.78
Deep-Palm: 0.04
96 - - -
GPS-Palm: 0.78
Deep-Palm: 0.04
99 - - -
Deep-Palm: 0.25
119 - - -
GPS-Palm: 0.68
Deep-Palm: 0.70
123 - - -
Deep-Palm: 0.64
127 - - -
GPS-Palm: 0.69
Deep-Palm: 0.53
131 - - -
GPS-Palm: 0.76
Deep-Palm: 0.13
132 - - -
GPS-Palm: 0.74
Deep-Palm: 0.20
137 SWISSPALM DBPTM CYSMODDB LITAF-like zinc ribbon domain
HeLa (29575903)
-
Deep-Palm: 0.33
148 - - -
Deep-Palm: 0.57
151 - - -
GPS-Palm: 0.75
Deep-Palm: 0.09
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)
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
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
116 W → C 0.002747 SNP Missense Mutation LIHC
137 C → C 0.001887 SNP Silent UCEC
160 R → C 0.001887 SNP Missense Mutation UCEC