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. |
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