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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A140VKH4 CAPN5 Calpain-5 Homo sapiens (Human) 640 aa

Protein Details: A0A140VKH4 (CAPN5)

Protein Information
AccessionA0A140VKH4
Protein NamesCalpain-5
Gene SymbolCAPN5
OrganismHomo sapiens (Human)
Length640 aa
IsoformsNo isoforms
Related PMIDs 22496122 36430497 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
1-501MFSCVKPYED11QNYSALRRDC21RRRKVLFEDP31LFPATDDSLY41YKGTPGPAVR
51-10051WKRPKGICED61PRLFVDGISS71HDLHQGQVGN81CWFVAACSSL91ASRESLWQKV
101-150101IPDWKEQEWD111PEKPNAYAGI121FHFHFWRFGE131WVDVVIDDRL141PTVNNQLIYC
151-200151HSNSRNEFWC161ALVEKAYAKL171AGCYQALDGG181NTADALVDFT191GGVSEPIDLT
201-250201EGDFANDETK211RNQLFERMLK221VHSRGGLISA231SIKAVTAADM241EARLACGLVK
251-300251GHAYAVTDVR261KVRLGHGLLA271FFKSEKLDMI281RLRNPWGERE291WNGPWSDTSE
301-350301EWQKVSKSER311EKMGVTVQDD321GEFWMTFEDV331CRYFTDIIKC341RVINTSHLSI
351-400351HKTWEEARLH361GAWTLHEDPR371QNRGGGCINH381KDTFFQNPQY391IFEVKKPEDE
401-450401VLICIQQRPK411RSTRREGKGE421NLAIGFDIYK431VEENRQYRMH441SLQHKAASSI
451-500451YINSRSVFLR461TDQPEGRYVI471IPTTFEPGHT481GEFLLRVFTD491VPSNCRELRL
501-550501DEPPHTCWSS511LCGYPQLVTQ521VHVLGAAGLK531DSPTGANSYV541IIKCEGDKVR
551-600551SAVQKGTSTP561EYNVKGIFYR571KKLSQPITVQ581VWNHRVLKDE591FLGQVHLKAD
601-640601PDNLQALHTL611HLRDRNSRQP621SNLPGTVAVH631ILSSTSLMAV
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
4 - - -
GPS-Palm: 0.93
Deep-Palm: 0.01
20 Papain-like cysteine peptidase superfamily - -
GPS-Palm: 0.83
Deep-Palm: 0.80
58 - - -
GPS-Palm: 0.78
Deep-Palm: 0.86
81 - - -
Deep-Palm: 0.19
87 - - -
GPS-Palm: 0.79
Deep-Palm: 0.22
150 - -
LNCaP (31251020)
cerebral cortex (36430497)
Deep-Palm: 0.25
160 - -
LNCaP (31251020)
cerebral cortex (36430497)
Deep-Palm: 0.30
173 - - -
GPS-Palm: 0.87
Deep-Palm: 0.95
246 - - -
GPS-Palm: 0.79
Deep-Palm: 0.92
331 - - -
GPS-Palm: 0.70
Deep-Palm: 0.02
340 - - -
GPS-Palm: 0.70
Deep-Palm: 0.06
377 - - -
GPS-Palm: 0.68
Deep-Palm: 0.10
404 - -
cerebral cortex (36430497)
GPS-Palm: 0.92
Deep-Palm: 0.88
495 - -
LNCaP (31251020)
cerebral cortex (36430497)
GPS-Palm: 0.89
Deep-Palm: 0.80
507 - -
cerebral cortex (36430497)
Deep-Palm: 0.54
512 - -
cerebral cortex (36430497)
Deep-Palm: 0.80
544 - - -
GPS-Palm: 0.80
Deep-Palm: 0.83
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
cerebral cortex
Specificity: 0.364
4/4 (100.0%)
1
EC cell
Specificity: 0.091
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.667
4
Cerebral Cortex (Mass)
Specificity: 0.364
4/4 (100.0%)
2
LNCaP cells (Mass)
Specificity: 0.182
2/4 (50.0%)
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
254 Y → C 0.002427 SNP Missense Mutation BLCA
263 R → C 0.002033 SNP Missense Mutation LUSC
267 G → C 0.002545 SNP Missense Mutation GBM
283 R → C 0.003460 SNP Missense Mutation CESC
286 W → C 0.003460 SNP Missense Mutation CESC
373 R → C 0.002288 SNP Missense Mutation STAD
419 G → C 0.002506 SNP Missense Mutation COAD
467 R → C 0.007299 SNP Missense Mutation READ
499 R → C 0.001887 SNP Missense Mutation UCEC
570 R → C 0.005618 SNP Missense Mutation PAAD