Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| P31943 | HNRNPH1 | Heterogeneous nuclear ribonucleoprotein H (hnRNP … | Homo sapiens (Human) | 449 aa |
Protein Details: P31943 (HNRNPH1)
Protein Information
| Accession | P31943 |
|---|---|
| Protein Names | Heterogeneous nuclear ribonucleoprotein H (hnRNP H) [Cleaved into: Heterogeneous nuclear ribonucleoprotein H, N-terminally processed] |
| Gene Symbol | HNRNPH1 |
| Organism | Homo sapiens (Human) |
| Length | 449 aa |
| Isoforms | No isoforms |
| Related PMIDs | 29575903 29733200 31251020 36430497 31251020 (mass) 32651440 (mass) 36430497 (mass) |
| Database Sources | CysModDBdbPTMSwissPalm |
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
Experimental Database High Prediction Non-palmitylated Cys
1-501MMLGTEGGEG11FVVKVRGLPW21SCSADEVQRF31FSDCKIQNGA41QGIRFIYTRE
51-10051GRPSGEAFVE61LESEDEVKLA71LKKDRETMGH81RYVEVFKSNN91VEMDWVLKHT
101-150101GPNSPDTAND111GFVRLRGLPF121GCSKEEIVQF131FSGLEIVPNG141ITLPVDFQGR
151-200151STGEAFVQFA161SQEIAEKALK171KHKERIGHRY181IEIFKSSRAE191VRTHYDPPRK
201-250201LMAMQRPGPY211DRPGAGRGYN221SIGRGAGFER231MRRGAYGGGY241GGYDDYNGYN
251-300251DGYGFGSDRF261GRDLNYCFSG271MSDHRYGDGG281STFQSTTGHC291VHMRGLPYRA
301-350301TENDIYNFFS311PLNPVRVHIE321IGPDGRVTGE331ADVEFATHED341AVAAMSKDKA
351-400351NMQHRYVELF361LNSTAGASGG371AYEHRYVELF381LNSTAGASGG391AYGSQMMGGM
401-449401GLSNQSSYGG411PASQQLSGGY421GGGYGGQSSM431SGYDQVLQEN441SSDFQSNIA
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 22 | SWISSPALM DBPTM CYSMODDB | Nucleotide-binding alpha-beta plait domain superfamily RNA-binding domain superfamily |
SW480 cell line
(26865113)
|
cerebral cortex
(36430497)
|
GPS-Palm: 0.87
Deep-Palm: 0.86
|
| 34 | RNA-binding domain superfamily Epithelial Splicing Regulatory Nucleotide-binding alpha-beta plait domain superfamily | - | - |
GPS-Palm: 0.76
Deep-Palm: 0.18
|
|
| 122 | - | - | - |
GPS-Palm: 0.94
Deep-Palm: 0.96
|
|
| 267 | - | - | - |
GPS-Palm: 0.66
Deep-Palm: 0.32
|
|
| 290 | - | - | - |
Deep-Palm: 0.33
|
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)
• 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): 0.333
3
LNCaP
Specificity: 0.273
3/3 (100.0%)
2
HAP1 cell
Specificity: 0.182
2/2 (100.0%)
2
cerebral cortex
Specificity: 0.182
2/2 (100.0%)
1
HeLa cell
Specificity: 0.091
1/1 (100.0%)
1
293T cell
Specificity: 0.091
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
2
Cerebral Cortex (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 |
|---|---|---|---|---|---|
| 17 | G → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 22 | C → Y | 0.001764 | SNP | Missense Mutation | LUAD |
| 51 | G → C | 0.001969 | SNP | Missense Mutation | HNSC |
| 210 | Y → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 329 | G → C | 0.002294 | SNP | Missense Mutation | OV |
| 388 | S → C | 0.002033 | SNP | Missense Mutation | LUSC |