Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q9NP58-4 ABCB6 ATP-binding cassette sub-family B member … Homo sapiens (Human) 796 aa

Protein Details: Q9NP58-4 (ABCB6)

Protein Information
AccessionQ9NP58-4
Protein NamesATP-binding cassette sub-family B member 6 (ABC-type heme transporter ABCB6) (EC 7.6.2.5) (Mitochondrial ABC transporter 3) (Mt-ABC transporter 3) (P-glycoprotein-related protein) (Ubiquitously-expressed mammalian ABC half transporter)
Gene SymbolABCB6
OrganismHomo sapiens (Human)
Length796 aa
Isoforms
Related PMIDs 29575903 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
1-501MVTVGNYCEA11EGPVGPAWMQ21DGLSPCFFFT31LVPSTRMALG41TLALVLALPC
51-10051RRRERPAGAD61SLSWGAGPRI71SPYVLQLLLA81TLQAALPLAG91LAGRVGTARG
101-150101APLPSYLLLA111SVLESLAGAC121GLWLLVVERS131QARQRLAMGI141WIKFRHSPGL
151-200151LLLWTVAFAA161ENLALVSWNS171PQWWWARADL181GQQVRSAAQQ191STWRDFGRKL
201-250201RLLSGYLWPR211GSPALQLVVL221ICLGLMGLER231ALNVLVPIFY241RNIVNLLTEK
251-300251APWNSLAWTV261TSYVFLKFLQ271GGGTGSTGFV281SNLRTFLWIR291VQQFTSRRVE
301-350301LLIFSHLHEL311SLRWHLGRRT321GEVLRIADRG331TSSVTGLLSY341LVFNVIPTLA
351-400351DIIIGIIYFS361MFFNAWFGLI371VFLCMSLYLT381LTIVVTEWRT391KFRRAMNTQE
401-450401NATRARAVDS411LLNFETVKYY421NAESYEVERY431REAIIKYQGL441EWKSSASLVL
451-500451LNQTQNLVIG461LGLLAGSLLC471AYFVTEQKLQ481VGDYVLFGTY491IIQLYMPLNW
501-550501FGTYYRMIQT511NFIDMENMFD521LLKEETEVKD531LPGAGPLRFQ541KGRIEFENVH
551-600551FSYADGRETL561QDVSFTVMPG571QTLALVGPSG581AGKSTILRLL591FRFYDISSGC
601-650601IRIDGQDISQ611VTQASLRSHI621GVVPQDTVLF631NDTIADNIRY641GRVTAGNDEV
651-700651EAAAQAAGIH661DAIMAFPEGY671RTQVGERGLK681LSGGEKQRVA691IARTILKAPG
701-750701IILLDEATSA711LDTSNERAIQ721ASLAKVCANR731TTIVVAHRLS741TVVNADQILV
751-796751IKDGCIVERG761RHEALLSRGG771VYADMWQLQQ781GQEETSEDTK791PQTMER
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
8 ATP-binding cassette sub-family B member 6, N-terminal five TM domain - -
Deep-Palm: 0.02
26 ATP-binding cassette sub-family B member 6, N-terminal five TM domain - -
Deep-Palm: 0.82
50 -
HeLa (29575903)
-
GPS-Palm: 0.95
Deep-Palm: 0.99
120 - - -
GPS-Palm: 0.87
Deep-Palm: 0.97
222 - - -
GPS-Palm: 0.87
268 - - -
Deep-Palm: 0.98
420 - - -
Deep-Palm: 0.05
470 - - -
GPS-Palm: 0.84
516 - - -
Deep-Palm: 0.97
600 - - -
GPS-Palm: 0.89
646 - - -
Deep-Palm: 0.97
727 - - -
GPS-Palm: 0.86
755 - - -
GPS-Palm: 0.90
773 - - -
Deep-Palm: 0.97
801 - - -
Deep-Palm: 0.98
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
4
LNCaP
Specificity: 0.667
4/4 (100.0%)
1
HeLa cell
Specificity: 0.167
1/1 (100.0%)
1
heart
Specificity: 0.167
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
210 R → C 0.001887 SNP Missense Mutation UCEC
214 Y → C 0.001764 SNP Missense Mutation LUAD
286 Y → C 0.002294 SNP Missense Mutation OV
359 R → C 0.002506 SNP Missense Mutation COAD
409 F → C 0.002141 SNP Missense Mutation SKCM
471 Y → C 0.001887 SNP Missense Mutation UCEC
513 S → C 0.001014 SNP Missense Mutation BRCA
634 R → C 0.001887 SNP Missense Mutation UCEC