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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
K7ER00 FARSA Phenylalanine--tRNA ligase alpha subunit (EC … Homo sapiens (Human) 548 aa

Protein Details: K7ER00 (FARSA)

Protein Information
AccessionK7ER00
Protein NamesPhenylalanine--tRNA ligase alpha subunit (EC 6.1.1.20) (Phenylalanyl-tRNA synthetase alpha subunit)
Gene SymbolFARSA
OrganismHomo sapiens (Human)
Length548 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
1-501MEPGWRWELS11PMHLLRLRRH21TQDDDTLSPV31LQLDTFKMAV41HTPVPVAELL
51-10051LRRLEASDGG61LDSAELAAEL71GMEHQAVVGA81VKSLQALGEV91IEAELRSTKH
101-150101WELTAEGEEI111AREGSHEARV121FRSIPPEGLA131QSELMRLPSG141KVGFSKAMSN
151-200151KWIRVDKSAA161DGPRVFRVVD171SMEDEVQRRL181QLVRGGQAEK191LGEKERSELR
201-250201KRKLLAEVTL211KTYWVSKGSA221FSTSISKQET231ELSPEMISSG241SWRDRPFKPY
251-300251NFLAHGVLPD261SGHLHPLLKV271RSQFRQIFLE281MGFTEMPTDN291FIESSFWNFD
301-350301ALFQPQQHPA311RDQHDTFFLR321DPAEALQLPM331DYVQRVKRTH341SQGGYGSQGY
351-400351KYNWKLDEAR361KNLLRTHTTS371ASARALYRLA381QKKPFTPVKY391FSIDRVFRNE
401-450401TLDATHLAEF411HQIEGVVADH421GLTLGHLMGV431LREFFTKLGI441TQLRFKPAYN
451-500451PYTEPSMEVF461SYHQGLKKWV471EVGNSGVFRP481EMLLPMGLPE491NVSVIAWGLS
501-548501LERPTMIKYG511INNIRELVGH521KVNLQMVYDS531PLCRLDAEPR541PPPTQEAA
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
533 SWISSPALM DBPTM CYSMODDB - - -
Deep-Palm: 0.88
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
429 W → C 0.002427 SNP Missense Mutation BLCA
439 R → C 0.002294 SNP Missense Mutation OV
463 R → C 0.003460 SNP Missense Mutation CESC