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UniProt ID Gene Symbol Protein Name Organism Length Action
Q96EK9 KTI12 Protein KTI12 homolog Homo sapiens (Human) 354 aa

Protein Details: Q96EK9 (KTI12)

Protein Information
AccessionQ96EK9
Protein NamesProtein KTI12 homolog
Gene SymbolKTI12
OrganismHomo sapiens (Human)
Length354 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
1-501MPLVVFCGLP11YSGKSRRAEE21LRVALAAEGR31AVYVVDDAAV41LGAEDPAVYG
51-10051DSAREKALRG61ALRASVERRL71SRHDVVILDS81LNYIKGFRYE91LYCLARAART
101-150101PLCLVYCVRP111GGPIAGPQVA121GANENPGRNV131SVSWRPRAEE141DGRAQAAGSS
151-200151VLRELHTADS161VVNGSAQADV171PKELEREESG181AAESPALVTP191DSEKSAKHGS
201-250201GAFYSPELLE211ALTLRFEAPD221SRNRWDRPLF231TLVGLEEPLP241LAGIRSALFE
251-300251NRAPPPHQST261QSQPLASGSF271LHQLDQVTSQ281VLAGLMEAQK291SAVPGDLLTL
301-350301PGTTEHLRFT311RPLTMAELSR321LRRQFISYTK331MHPNNENLPQ341LANMFLQYLS
351-354351QSLH
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
7 Protein KTI12/L-seryl-tRNA(Sec) kinase - -
GPS-Palm: 0.94
Deep-Palm: 0.15
93 - - -
GPS-Palm: 0.85
Deep-Palm: 0.90
103 SWISSPALM DBPTM CYSMODDB Chromatin associated protein KTI12
HeLa (37611173)
-
GPS-Palm: 0.91
Deep-Palm: 0.96
107 SWISSPALM DBPTM CYSMODDB Chromatin associated protein KTI12 - -
GPS-Palm: 0.90
Deep-Palm: 0.97
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
72 R → C 0.002033 SNP Missense Mutation LUSC
179 S → C 0.003460 SNP Missense Mutation CESC
320 R → C 0.001014 SNP Missense Mutation BRCA
323 R → C 0.017544 SNP Missense Mutation UCS