Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A7I2V5T4 ACO2 Aconitate hydratase, mitochondrial (Aconitase) (EC … Homo sapiens (Human) 775 aa

Protein Details: A0A7I2V5T4 (ACO2)

Protein Information
AccessionA0A7I2V5T4
Protein NamesAconitate hydratase, mitochondrial (Aconitase) (EC 4.2.1.3)
Gene SymbolACO2
OrganismHomo sapiens (Human)
Length775 aa
IsoformsNo isoforms
Related PMIDs 26876311 31251020 (mass) 32651440 (mass) 36430497 (mass)
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MAPYSLLVTR11LQKALGVRQY21HVASVLCQRA31KVAMSHFEPN41EYIHYDLLEK
51-10051NINIVRKRLN61RPLTLSEKIV71YGHLDDPASQ81EIERGKSYLR91LRPDRVAMQD
101-150101ATAQMAMLQF111ISSGLSKVAV121PSTIHCDHLI131EAQVGGEKDL141RRAKDINQEV
151-200151YNFLATAGAK161YGVGFWKPGS171GIIHQIILEN181YAYPGVLLIG191TDSHTPNGGG
201-250201LGGICIGVGG211ADAVDVMAGI221PWELKCPKVI231GVKLTGSLSG241WSSPKDVILK
251-300251VAGILTVKGG261TGAIVEYHGP271GVDSISCTGM281ATICNMGAEI291GATTSVFPYN
301-350301HRMKKYLSKT311GREADEFKDH321LVPDPGCHYD331QLIEINLSEL341KPHINGPFTP
351-400351DLAHPVAEVG361KVAEKEGWPL371DIRVGLIGSC381TNSSYEDMGR391SAAVAKQALA
401-450401HGLKCKSQFT411ITPGSEQIRA421TIERDGYAQI431LRDLGGIVLA441NACGPCIGQW
451-500451DRKDIKKGEK461NTIVTSYNRN471FTGRNDANPE481THAFVTSPEI491VTALAIAGTL
501-550501KFNPETDYLT511GTDGKKFRLE521APDADELPKG531EFDPGQDTYQ541HPPKDSSGQH
551-600551VDVSPTSQRL561QLLEPFDKWD571GKDLEDLQIL581IKVKGKCTTD591HISAAGPWLK
601-650601FRGHLDNISN611NLLIGAINIE621NGKANSVRNA631VTQEFGPVPD641TARYYKKHGI
651-700651RWVVIGDENY661GEGSSREHAA671LEPRHLGGRA681IITKSFARIH691ETNLKKQGLL
701-750701PLTFADPADY711NKIHPVDKLT721IQGLKDFTPG731KPLKCIIKHP741NGTQETILLN
751-775751HTFNETQIEW761FRAGSALNRM771KELQQ
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
27 - - -
GPS-Palm: 0.84
Deep-Palm: 0.89
126 - -
cerebral cortex (36430497)
Deep-Palm: 0.92
205 - - -
GPS-Palm: 0.73
Deep-Palm: 0.83
226 - - -
GPS-Palm: 0.83
Deep-Palm: 0.96
277 - -
cerebral cortex (36430497)
Deep-Palm: 0.29
284 - -
cerebral cortex (36430497)
Deep-Palm: 0.34
327 - - -
Deep-Palm: 0.77
380 - -
cerebral cortex (36430497)
LNCaP (31251020)
GPS-Palm: 0.86
Deep-Palm: 0.96
405 - - -
GPS-Palm: 0.87
Deep-Palm: 0.97
443 - -
cerebral cortex (36430497)
GPS-Palm: 0.94
Deep-Palm: 0.97
446 - -
cerebral cortex (36430497)
GPS-Palm: 0.94
Deep-Palm: 0.96
587 - -
cerebral cortex (36430497)
LNCaP (31251020)
Unknown (32651440)
GPS-Palm: 0.76
Deep-Palm: 0.89
735 - - -
Deep-Palm: 0.94
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): 1.000
1
frontal cortex
Specificity: 0.167
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.800
4
Cerebral Cortex (Mass)
Specificity: 0.667
4/4 (100.0%)
1
LNCaP cells (Mass)
Specificity: 0.167
1/4 (25.0%)
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
56 R → C 0.002141 SNP Missense Mutation SKCM
141 R → C 0.001887 SNP Missense Mutation UCEC
279 G → C 0.002033 SNP Missense Mutation LUSC
564 R → C 0.003774 SNP Missense Mutation UCEC
633 R → C 0.002288 SNP Missense Mutation STAD
679 R → C 0.002427 SNP Missense Mutation BLCA
740 C → C 0.001887 SNP Silent UCEC
284* C → ? 0.002545 SNP Nonsense Mutation GBM