Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q4KMQ2-3 ANO6 Anoctamin-6 (Small-conductance calcium-activated nonselective cation … Homo sapiens (Human) 892 aa

Protein Details: Q4KMQ2-3 (ANO6)

Protein Information
AccessionQ4KMQ2-3
Protein NamesAnoctamin-6 (Small-conductance calcium-activated nonselective cation channel) (SCAN channel) (Transmembrane protein 16F)
Gene SymbolANO6
OrganismHomo sapiens (Human)
Length892 aa
Isoforms
Related PMIDs 31251020 33636221
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MFCAAVLENL11GQTIVPDLGS21LESQHDFRTP31EFEEFNGKPD41SLFFNDGQRR
51-10051IDFVLVYEDE61SRKETNKKGT71NEKQRRKRQA81YESNLICHGL91QLEATRSVLD
101-150101DKLVFVKVHA111PWEVLCTYAE121IMHIKLPLKP131NDLKNRSSAF141GTLNWFTKVL
151-200151SVDESIIKPE161QEFFTAPFEK171NRMNDFYIVD181RDAFFNPATR191SRIVYFILSR
201-250201VKYQVINNVS211KFGINRLVNS221GIYKAAFPLH231DCKFRRQSED241PSCPNERYLL
251-300251YREWAHPRSI261YKKQPLDLIR271KYYGEKIGIY281FAWLGYYTQM291LLLAAVVGVA
301-350301CFLYGYLNQD311NCTWSKEVCH321PDIGGKIIMC331PQCDRLCPFW341KLNITCESSK
351-400351KLCIFDSFGT361LVFAVFMGVW371VTLFLEFWKR381RQAELEYEWD391TVELQQEEQA
401-450401RPEYEARCTH411VVINEITQEE421ERIPFTAWGK431CIRITLCASA441VFFWILLIIA
451-500451SVIGIIVYRL461SVFIVFSAKL471PKNINGTDPI481QKYLTPQTAT491SITASIISFI
501-550501IIMILNTIYE511KVAIMITNFE521LPRTQTDYEN531SLTMKMFLFQ541FVNYYSSCFY
551-600551IAFFKGKFVG561YPGDPVYWLG571KYRNEECDPG581GCLLELTTQL591TIIMGGKAIW
601-650601NNIQEVLLPW611IMNLIGRFHR621VSGSEKITPR631WEQDYHLQPM641GKLGLFYEYL
651-700651EMIIQFGFVT661LFVASFPLAP671LLALVNNILE681IRVDAWKLTT691QFRRLVPEKA
701-750701QDIGAWQPIM711QGIAILAVVT721NAMIIAFTSD731MIPRLVYYWS741FSVPPYGDHT
751-800751SYTMEGYINN761TLSIFKVADF771KNKSKGNPYS781DLGNHTTCRY791RDFRYPPGHP
801-850801QEYKHNIYYW811HVIAAKLAFI821IVMEHVIYSV831KFFISYAIPD841VSKRTKSKIQ
851-892851REKYLTQKLL861HENHLKDMTK871NMGVIAERMI881EAVDNNLRPK891SE
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
3 - - -
GPS-Palm: 0.96
105 - - -
Deep-Palm: 0.97
134 - - -
Deep-Palm: 0.61
250 - - -
Deep-Palm: 0.67
261 - - -
Deep-Palm: 0.44
319 - - -
Deep-Palm: 0.29
330 - - -
Deep-Palm: 0.09
337 - - -
Deep-Palm: 0.02
348 - - -
Deep-Palm: 0.07
351 - - -
Deep-Palm: 0.04
355 - - -
Deep-Palm: 0.22
364 - - -
Deep-Palm: 0.35
371 - - -
Deep-Palm: 0.35
426 - - -
Deep-Palm: 0.70
449 - - -
Deep-Palm: 0.49
455 - - -
Deep-Palm: 0.48
566 - - -
Deep-Palm: 0.08
595 - - -
Deep-Palm: 0.93
600 - - -
Deep-Palm: 0.93
806 - - -
Deep-Palm: 0.15
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): 0.667
2
LNCaP
Specificity: 0.667
2/2 (100.0%)
1
heart
Specificity: 0.333
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.
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
41 S → C 0.005435 SNP Missense Mutation ESCA
230 F → C 0.001887 SNP Missense Mutation UCEC
364 C → C 0.002506 SNP Silent COAD
422 Y → C 0.001887 SNP Missense Mutation UCEC
440 R → C 0.001887 SNP Missense Mutation UCEC
455 C → S 0.008130 SNP Missense Mutation THYM
568 Y → C 0.002506 SNP Missense Mutation COAD
576 F → C 0.001887 SNP Missense Mutation UCEC
659 G → C 0.001764 SNP Missense Mutation LUAD
712 R → C 0.003460 SNP Missense Mutation CESC
756 Y → C 0.002288 SNP Missense Mutation STAD
850 F → C 0.001887 SNP Missense Mutation UCEC
862 R → C 0.002506 SNP Missense Mutation COAD
862 R → C 0.001887 SNP Missense Mutation UCEC
868 C → C 0.002506 SNP Silent COAD