Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| P17861-2 | XBP1 | Isoform 2 of X-box-binding protein … | Homo sapiens (Human) | 376 aa |
Protein Details: P17861-2 (XBP1)
Protein Information
| Accession | P17861-2 |
|---|---|
| Protein Names | Isoform 2 of X-box-binding protein 1 |
| Gene Symbol | XBP1 |
| Organism | Homo sapiens (Human) |
| Length | 376 aa |
| Isoforms |
|
| Related PMIDs | No related PMIDs |
| Database Sources | SwissPalm |
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MVVVAAAPNP11ADGTPKVLLL21SGQPASAAGA31PAGQALPLMV41PAQRGASPEA
51-10051ASGGLPQARK61RQRLTHLSPE71EKALRRKLKN81RVAAQTARDR91KKARMSELEQ
101-150101QVVDLEEENQ111KLLLENQLLR121EKTHGLVVEN131QELRQRLGMD141ALVAEEEAEA
151-200151KGNEVRPVAG161SAESAAGAGP171VVTPPEHLPM181DSGGIDSSDS191ESDILLGILD
201-250201NLDPVMFFKC211PSPEPASLEE221LPEVYPEGPS231SLPASLSLSV241GTSSAKLEAI
251-300251NELIRFDHIY261TKPLVLEIPS271ETESQANVVV281KIEEAPLSPS291ENDHPEFIVS
301-350301VKEEPVEDDL311VPELGISNLL321SSSHCPKPSS331CLLDAYSDCG341YGGSLSPFSD
351-376351MSSLLGVNHS361WEDTFANELF371PQLISV
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 325 | SWISSPALM | - | - |
| 331 | SWISSPALM | - | - |
| 339 | SWISSPALM | - | - |
Conservation Scores
PhyloP
PhastCons
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 |
|---|---|---|---|---|---|
| 136 | R → C | 0.002545 | SNP | Missense Mutation | GBM |