| UniProt ID | MB3L1_HUMAN | |
|---|---|---|
| UniProt AC | Q8WWY6 | |
| Protein Name | Methyl-CpG-binding domain protein 3-like 1 | |
| Gene Name | MBD3L1 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 194 | |
| Subcellular Localization | Nucleus . Nuclear, in large foci. | |
| Protein Description | Transcriptional repressor.. | |
| Protein Sequence | MAKSSQRKQRDCVNQCKSKPGLSTSIPLRMSSYTFKRPVTRITPHPGNEVRYHQWEESLEKPQQVCWQRRLQGLQAYSSAGELSSTLDLANTLQKLVPSYTGGSLLEDLASGLEHSCPMPHLACSSDAVEIIPAEGVGISQLLCKQFLVTEEDIRKQEGKVKTVRERLAIALIADGLANEAEKVRDQEGRPEKR | |
| 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 |
|---|---|---|---|---|---|
| 23 | Phosphorylation | CKSKPGLSTSIPLRM HHCCCCCCCCCCEEC | 26.48 | 26657352 | |
| 25 | Phosphorylation | SKPGLSTSIPLRMSS CCCCCCCCCCEECCE | 20.87 | 26657352 | |
| 77 | Phosphorylation | RLQGLQAYSSAGELS HHHHHHHHHCCCHHH | 7.09 | 21214269 | |
| 78 | Phosphorylation | LQGLQAYSSAGELSS HHHHHHHHCCCHHHH | 19.41 | 21214269 | |
| 92 | Phosphorylation | STLDLANTLQKLVPS HHHHHHHHHHHHCCC | 25.59 | - |
| 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 MB3L1_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of MB3L1_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 MB3L1_HUMAN !! | ||||||
| Kegg Drug | ||||||
|---|---|---|---|---|---|---|
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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