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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P98194-2 ATP2C1 Calcium-transporting ATPase type 2C member … Homo sapiens (Human) 888 aa

Protein Details: P98194-2 (ATP2C1)

Protein Information
AccessionP98194-2
Protein NamesCalcium-transporting ATPase type 2C member 1 (ATPase 2C1) (EC 7.2.2.10) (ATP-dependent Ca(2+) pump PMR1) (Ca(2+)/Mn(2+)-ATPase 2C1) (Secretory pathway Ca(2+)-transporting ATPase type 1) (SPCA1)
Gene SymbolATP2C1
OrganismHomo sapiens (Human)
Length888 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
1-501MKVARFQKIP11NGENETMIPV21LTSKKASELP31VSEVASILQA41DLQNGLNKCE
51-10051VSHRRAFHGW61NEFDISEDEP71LWKKYISQFK81NPLIMLLLAS91AVISVLMHQF
101-150101DDAVSITVAI111LIVVTVAFVQ121EYRSEKSLEE131LSKLVPPECH141CVREGKLEHT
151-200151LARDLVPGDT161VCLSVGDRVP171ADLRLFEAVD181LSIDESSLTG191ETTPCSKVTA
201-250201PQPAATNGDL211ASRSNIAFMG221TLVRCGKAKG231VVIGTGENSE241FGEVFKMMQA
251-300251EEAPKTPLQK261SMDLLGKQLS271FYSFGIIGII281MLVGWLLGKD291ILEMFTISVS
301-350301LAVAAIPEGL311PIVVTVTLAL321GVMRMVKKRA331IVKKLPIVET341LGCCNVICSD
351-400351KTGTLTKNEM361TVTHIFTSDG371LHAEVTGVGY381NQFGEVIVDG391DVVHGFYNPA
401-450401VSRIVEAGCV411CNDAVIRNNT421LMGKPTEGAL431IALAMKMGLD441GLQQDYIRKA
451-500451EYPFSSEQKW461MAVKCVHRTQ471QDRPEICFMK481GAYEQVIKYC491TTYQSKGQTL
501-550501TLTQQQRDVY511QQEKARMGSA521GLRVLALASG531PELGQLTFLG541LVGIIDPPRT
551-600551GVKEAVTTLI561ASGVSIKMIT571GDSQETAVAI581ASRLGLYSKT591SQSVSGEEID
601-650601AMDVQQLSQI611VPKVAVFYRA621SPRHKMKIIK631SLQKNGSVVA641MTGDGVNDAV
651-700651ALKAADIGVA661MGQTGTDVCK671EAADMILVDD681DFQTIMSAIE691EGKGIYNNIK
701-750701NFVRFQLSTS711IAALTLISLA721TLMNFPNPLN731AMQILWINII741MDGPPAQSLG
751-800751VEPVDKDVIR761KPPRNWKDSI771LTKNLILKIL781VSSIIIVCGT791LFVFWRELRD
801-850801NVITPRDTTM811TFTCFVFFDM821FNALSSRSQT831KSVFEIGLCS841NRMFCYAVLG
851-888851SIMGQLLVIY861FPPLQKVFQT871ESLSILGLAL881GEEWTAAG
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
49 Cation-transporting P-type ATPase, N-terminal P-type ATPase, transmembrane domain superfamily - -
Deep-Palm: 0.69
139 - - -
Deep-Palm: 0.98
141 - - -
GPS-Palm: 0.90
Deep-Palm: 0.98
162 - - -
Deep-Palm: 0.98
195 - - -
Deep-Palm: 0.84
225 - - -
Deep-Palm: 0.96
343 - - -
GPS-Palm: 0.90
Deep-Palm: 0.98
344 - - -
GPS-Palm: 0.92
Deep-Palm: 0.98
348 - - -
Deep-Palm: 0.97
409 - - -
Deep-Palm: 0.42
411 - - -
Deep-Palm: 0.55
465 - - -
Deep-Palm: 0.13
477 - - -
Deep-Palm: 0.08
490 - - -
Deep-Palm: 0.75
669 - - -
Deep-Palm: 0.89
788 - - -
Deep-Palm: 0.87
814 - - -
Deep-Palm: 0.14
839 - - -
Deep-Palm: 0.87
845 - - -
Deep-Palm: 0.54
889 - - -
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): 0.800
4
LNCaP
Specificity: 0.800
4/4 (100.0%)
1
heart
Specificity: 0.200
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
143 R → C 0.001887 SNP Missense Mutation UCEC
195 C → Vfs*4 0.001014 DEL Frame Shift Del BRCA
409 C → C 0.002506 SNP Silent COAD
490 C → Y 0.001969 SNP Missense Mutation HNSC
760 R → C 0.002506 SNP Missense Mutation COAD
814 C → C 0.002288 SNP Silent STAD
972 C → F 0.001764 SNP Missense Mutation LUAD