| UniProt ID | WBP1_HUMAN | |
|---|---|---|
| UniProt AC | Q96G27 | |
| Protein Name | WW domain-binding protein 1 | |
| Gene Name | WBP1 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 269 | |
| Subcellular Localization | ||
| Protein Description | ||
| Protein Sequence | MARASSGNGSEEAWGALRAPQQQLRELCPGVNNQPYLCESGHCCGETGCCTYYYELWWFWLLWTVLILFSCCCAFRHRRAKLRLQQQQRQREINLLAYHGACHGAGPFPTGSLLDLRFLSTFKPPAYEDVVHRPGTPPPPYTVAPGRPLTASSEQTCCSSSSSCPAHFEGTNVEGVSSHQSAPPHQEGEPGAGVTPASTPPSCRYRRLTGDSGIELCPCPASGEGEPVKEVRVSATLPDLEDYSPCALPPESVPQIFPMGLSSSEGDIP | |
| Overview of Protein Modification Sites with Functional and Structural Information | ||
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* ASA = Accessible Surface Area
| Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
|---|---|---|---|---|---|
| 110 | Phosphorylation | HGAGPFPTGSLLDLR CCCCCCCCCCCCHHH | 39.52 | 24719451 | |
| 112 | Phosphorylation | AGPFPTGSLLDLRFL CCCCCCCCCCHHHHH | 28.39 | 28348404 | |
| 136 | Phosphorylation | DVVHRPGTPPPPYTV CCCCCCCCCCCCCCC | 34.99 | - | |
| 209 | Phosphorylation | SCRYRRLTGDSGIEL CCCCCCCCCCCCCEE | 36.81 | 23401153 | |
| 212 | Phosphorylation | YRRLTGDSGIELCPC CCCCCCCCCCEEECC | 42.91 | 29978859 |
| Modified Location | Modified Residue | Modification | Type of Upstream Proteins | Gene Name of Upstream Proteins | UniProt AC of Upstream Proteins | Sources |
|---|---|---|---|---|---|---|
Oops, there are no upstream regulatory protein records of WBP1_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of WBP1_HUMAN !! | ||||||
* Distance = the distance between SAP position and PTM sites.
| Modified Location | Modification | Variant Position (Distance <= 10) |
Residue Change | SAP | Related Disease | Reference |
|---|---|---|---|---|---|---|
Oops, there are no SNP-PTM records of WBP1_HUMAN !! | ||||||
| Kegg Drug | ||||||
|---|---|---|---|---|---|---|
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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