| UniProt ID | OCEL1_HUMAN | |
|---|---|---|
| UniProt AC | Q9H607 | |
| Protein Name | Occludin/ELL domain-containing protein 1 | |
| Gene Name | OCEL1 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 264 | |
| Subcellular Localization | ||
| Protein Description | ||
| Protein Sequence | MHNPDGSASPTADPGSELQTLGQAARRPPPPRAGHDAPRRTRPSARKPLSCFSRRPMPTREPPKTRGSRGHLHTHPPGPGPPLQGLAPRGLKTSAPRPPCQPQPGPHKAKTKKIVFEDELLSQALLGAKKPIGAIPKGHKPRPHPVPDYELKYPPVSSERERSRYVAVFQDQYGEFLELQHEVGCAQAKLRQLEALLSSLPPPQSQKEAQVAARVWREFEMKRMDPGFLDKQARCHYLKGKLRHLKTQIQKFDDQGDSEGSVYF | |
| 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 |
|---|---|---|---|---|---|
| 50 | Phosphorylation | PSARKPLSCFSRRPM CCCCCCCCCCCCCCC | 22.95 | 24719451 | |
| 53 | Phosphorylation | RKPLSCFSRRPMPTR CCCCCCCCCCCCCCC | 31.54 | 24719451 | |
| 59 | Phosphorylation | FSRRPMPTREPPKTR CCCCCCCCCCCCCCC | 41.22 | 22468782 | |
| 122 | Phosphorylation | VFEDELLSQALLGAK ECCHHHHHHHHHCCC | 26.49 | - | |
| 247 | Phosphorylation | GKLRHLKTQIQKFDD HHHHHHHHHHHHHCC | 36.95 | - |
| 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 OCEL1_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of OCEL1_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 OCEL1_HUMAN !! | ||||||
| Kegg Drug | ||||||
|---|---|---|---|---|---|---|
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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