Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
1 structures for Q01265
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q01265-F1 | Predicted | AlphaFoldDB |
No variants for Q01265
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q01265 | |||||
No associated diseases with Q01265
No GO annotations of cellular component
| Name | Definition |
|---|---|
| No GO annotations for cellular component |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
2 GO annotations of biological process
| Name | Definition |
|---|---|
| phosphorelay signal transduction system | A conserved series of molecular signals found in prokaryotes and eukaryotes; involves autophosphorylation of a histidine kinase and the transfer of the phosphate group to an aspartate that then acts as a phospho-donor to response regulator proteins. |
| regulation of DNA-templated transcription | Any process that modulates the frequency, rate or extent of cellular DNA-templated transcription. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| DQEIVVKSMA | MEKVYELACR | VADSDATIFL | QGETGVGKEV | LARTIHNSSI | RKEAPFIKVN |
| 70 | 80 | 90 | 100 | 110 | 120 |
| CGAIPESIME | SELFGYSKGT | FTGGNKDGKK | GLAQAAHNGT | LFLDEIGELP | LNLQAKLLQL |
| 130 | 140 | 150 | 160 | 170 | 180 |
| LNEKQFTPLG | EIKPVQVDVR | FIAATNRNLE | DMVREGTFRE | DLYYRLFVIP | ITIPSLSERR |
| 190 | 200 | 210 | 220 | 230 | 240 |
| EDIPFLINHF | LETFNHKYKL | YKTIDKEVVQ | FFIDYEWKGN | VRELQNTIER | LVLISSAQQI |
| 250 | 260 | 270 | 280 | 290 | |
| ELSDLSDKFK | KATSHTKGGI | SGEGLNLKQK | MEQFEKQILI | QTLESSNTMK | EASKN |