| UniProt ID | NR0B2_HUMAN | |
|---|---|---|
| UniProt AC | Q15466 | |
| Protein Name | Nuclear receptor subfamily 0 group B member 2 | |
| Gene Name | NR0B2 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 257 | |
| Subcellular Localization | Nucleus . Cytoplasm . Colocalizes with NEUROD1 in the nucleus. | |
| Protein Description | Acts as a transcriptional regulator. Acts as a negative regulator of receptor-dependent signaling pathways. Specifically inhibits transactivation of the nuclear receptor with whom it interacts. Inhibits transcriptional activity of NEUROD1 on E-box-containing promoter by interfering with the coactivation function of the p300/CBP-mediated transcription complex for NEUROD1.. | |
| Protein Sequence | MSTSQPGACPCQGAASRPAILYALLSSSLKAVPRPRSRCLCRQHRPVQLCAPHRTCREALDVLAKTVAFLRNLPSFWQLPPQDQRRLLQGCWGPLFLLGLAQDAVTFEVAEAPVPSILKKILLEEPSSSGGSGQLPDRPQPSLAAVQWLQCCLESFWSLELSPKEYACLKGTILFNPDVPGLQAASHIGHLQQEAHWVLCEVLEPWCPAAQGRLTRVLLTASTLKSIPTSLLGDLFFRPIIGDVDIAGLLGDMLLLR | |
| Overview of Protein Modification Sites with Functional and Structural Information | ||
|
|
||
* ASA = Accessible Surface Area
| Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
|---|---|---|---|---|---|
| 54 | Symmetric dimethylarginine | VQLCAPHRTCREALD CEECCCCCHHHHHHH | 34.17 | - | |
| 55 | Phosphorylation | QLCAPHRTCREALDV EECCCCCHHHHHHHH | 16.93 | - | |
| 57 | Methylation | CAPHRTCREALDVLA CCCCCHHHHHHHHHH | 31.45 | 57404601 | |
| 57 | Symmetric dimethylarginine | CAPHRTCREALDVLA CCCCCHHHHHHHHHH | 31.45 | - | |
| 116 | Phosphorylation | VAEAPVPSILKKILL HCCCCCCHHHHHHHC | 40.56 | 24719451 | |
| 170 | Acetylation | PKEYACLKGTILFNP HHHEEEEECEEEECC | 54.62 | 30422853 | |
| 238 | Dimethylation | LLGDLFFRPIIGDVD HHHHHHCCCCCCCCC | 17.74 | - | |
| 238 | Methylation | LLGDLFFRPIIGDVD HHHHHHCCCCCCCCC | 17.74 | 24379833 |
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of NR0B2_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 NR0B2_HUMAN !! | ||||||
| Kegg Disease | ||||||
|---|---|---|---|---|---|---|
| There are no disease associations of PTM sites. | ||||||
| OMIM Disease | ||||||
| 601665 | Obesity (OBESITY) | |||||
| Kegg Drug | ||||||
| There are no disease associations of PTM sites. | ||||||
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
loading...