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UniProt ID Gene Symbol Protein Name Organism Length Action
H3BU68 LPCAT2 Lysophosphatidylcholine acyltransferase 2 Homo sapiens (Human) 188 aa

Protein Details: H3BU68 (LPCAT2)

Protein Information
AccessionH3BU68
Protein NamesLysophosphatidylcholine acyltransferase 2
Gene SymbolLPCAT2
OrganismHomo sapiens (Human)
Length188 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
1-501XAPHSTFFDG11IACVVAGLPS21MVSRNENAQV31PLIGRLLRAV41QPVLVSRVDP
51-10051DSRKNTINEI61IKRTTSGGEW71PQILVFPEGT81CTNRSCLITF91KPGAFIPGVP
101-150101VQPVLLRYPN111KLDTVTWTWQ121GYTFIQLCML131TFCQLFTKVE141VEMFLFFWEG
151-188151SSKHCLKISS161FFCIFSLRRF171KRRITQRTRT181AHLLRLSF
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
13 - - -
Deep-Palm: 0.05
81 - - -
Deep-Palm: 0.92
86 SWISSPALM DBPTM CYSMODDB Acyltransferase - -
Deep-Palm: 0.94
128 - - -
Deep-Palm: 0.04
133 - - -
GPS-Palm: 0.70
Deep-Palm: 0.04
155 - - -
Deep-Palm: 0.54
163 - - -
GPS-Palm: 0.96
Deep-Palm: 0.81
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)
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
69 R → C 0.002141 SNP Missense Mutation SKCM
101 G → C 0.004219 SNP Missense Mutation SARC
113 F → C 0.002545 SNP Missense Mutation GBM
189 R → C 0.001969 SNP Missense Mutation HNSC
223 C → C 0.001887 SNP Silent UCEC
226 R → C 0.002141 SNP Missense Mutation SKCM
326 C → C 0.002288 SNP Silent STAD
483 Y → C 0.001764 SNP Missense Mutation LUAD
488 S → C 0.002545 SNP Missense Mutation GBM