Q8C779
Gene name |
Radx |
Protein name |
RPA-related protein RADX |
Names |
|
Species |
Mus musculus (Mouse) |
KEGG Pathway |
mmu:102871 |
EC number |
|
Protein Class |
|
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 Q8C779
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q8C779-F1 | Predicted | AlphaFoldDB |
35 variants for Q8C779
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| rs3412287365 | 67 | V>L | No | EVA | |
| rs3412184787 | 105 | Q>L | No | EVA | |
| rs3412052012 | 157 | E>G | No | EVA | |
| rs3389543140 | 183 | G>E | No | EVA | |
| rs3409412635 | 203 | K>M | No | EVA | |
| rs3412369949 | 255 | K>N | No | EVA | |
| rs3389556107 | 288 | K>E | No | EVA | |
| rs3412052361 | 297 | L>* | No | EVA | |
| rs3410678233 | 305 | K>Q | No | EVA | |
| rs3410678304 | 396 | S>N | No | EVA | |
| rs3389526230 | 460 | T>N | No | EVA | |
| rs3412369999 | 480 | D>N | No | EVA | |
| rs3412284767 | 503 | I>T | No | EVA | |
| rs3412288816 | 506 | Y>* | No | EVA | |
| rs3411719112 | 507 | Y>N | No | EVA | |
| rs3409412620 | 512 | V>M | No | EVA | |
| rs3412185804 | 533 | S>G | No | EVA | |
| rs3389580489 | 543 | Q>E | No | EVA | |
| rs3389569382 | 546 | E>G | No | EVA | |
| rs250766942 | 566 | H>Q | No | EVA | |
| rs1134122092 | 582 | R>H | No | EVA | |
| rs3389585308 | 595 | C>* | No | EVA | |
| rs223012567 | 618 | S>P | No | EVA | |
| rs3389585300 | 633 | P>L | No | EVA | |
| rs3412371558 | 662 | S>P | No | EVA | |
| rs29258376 | 684 | Q>R | No | EVA | |
| rs215871185 | 685 | D>A | No | EVA | |
| rs3389526247 | 695 | H>Y | No | EVA | |
| rs257762844 | 712 | H>Y | No | EVA | |
| rs3389580537 | 786 | C>Y | No | EVA | |
| rs3389585262 | 790 | S>N | No | EVA | |
| rs3389585276 | 792 | V>M | No | EVA | |
| rs3389576974 | 796 | A>G | No | EVA | |
| rs3412094916 | 830 | D>N | No | EVA | |
| rs3389586673 | 846 | I>V | No | EVA |
No associated diseases with Q8C779
No regional properties for Q8C779
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for Q8C779 | |||
2 GO annotations of cellular component
| Name | Definition |
|---|---|
| nuclear speck | A discrete extra-nucleolar subnuclear domain, 20-50 in number, in which splicing factors are seen to be localized by immunofluorescence microscopy. |
| replication fork | The Y-shaped region of a replicating DNA molecule, resulting from the separation of the DNA strands and in which the synthesis of new strands takes place. Also includes associated protein complexes. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| single-stranded DNA binding | Binding to single-stranded DNA. |
2 GO annotations of biological process
| Name | Definition |
|---|---|
| negative regulation of double-strand break repair via homologous recombination | Any process that stops, prevents, or reduces the frequency, rate or extent of double-strand break repair via homologous recombination. |
| regulation of DNA repair | Any process that modulates the frequency, rate or extent of DNA repair. |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSGESGQPQP | GPSHAGLYLE | HPERDQAGVP | GGVIRRADSQ | RRRSWIQKVI | EQITGSPRQC |
| 70 | 80 | 90 | 100 | 110 | 120 |
| VTLSEVVPVT | VLAVQRYLLE | DEPRDTVPKP | PLYCYDVTIS | DGVYQEKCYL | DPSLNFLVYQ |
| 130 | 140 | 150 | 160 | 170 | 180 |
| NILKVGIEMR | ISRVSCLYNE | KRLGQGILCI | DKVHCGESLD | VISVETPFRN | RAHEEKPERP |
| 190 | 200 | 210 | 220 | 230 | 240 |
| LRGGKSHYLA | LWNNEDPYGD | IWKTNKQPEE | FNFNNIKIIS | LSHLELTWNS | RKNFPALLVR |
| 250 | 260 | 270 | 280 | 290 | 300 |
| VLHKSKLRYY | GKPNKKMIEP | YQTYLEVADS | SGMVSVILWN | ALCPEWYKSL | RVGLVLLLQD |
| 310 | 320 | 330 | 340 | 350 | 360 |
| YTVKKSYPLR | IQPDPADPQM | KLISTMEICL | NLRDPPTNIV | IIPEKQLKSE | WKLPKLINRF |
| 370 | 380 | 390 | 400 | 410 | 420 |
| ITRSELDDMP | EKSICDVIGL | LSFVGRVQRS | KKKENSEDFW | SYRWIHITDG | TSEQPFIVQL |
| 430 | 440 | 450 | 460 | 470 | 480 |
| FSTSQPEVFE | NIYPMTYFVC | TQLKVVRNNS | QVPKLLYLTT | TNESRALTTG | GHRGLPYTYD |
| 490 | 500 | 510 | 520 | 530 | 540 |
| TKAKKIIQWI | KTKTNLEAKN | TVIGGYYPYP | PVPETFSKYS | RFIKAESLLT | TISEVKKVIE |
| 550 | 560 | 570 | 580 | 590 | 600 |
| DLQYREQKRI | AIQGIITAIK | YIPYKHSAGS | APAPEAFWNA | SRPSTSQAAG | KEDHCHERGS |
| 610 | 620 | 630 | 640 | 650 | 660 |
| KRSQDDRPMG | SQHFQYTSKV | LSLCAKRKIL | QGPSANPVPV | PQPHSSAQMK | GSKHNTPSQE |
| 670 | 680 | 690 | 700 | 710 | 720 |
| SSTAYTTGKS | RRITNDRWES | QLWQDKKFSL | RDHLHYGHVD | PESIPRKFIL | EHEKFLTQQF |
| 730 | 740 | 750 | 760 | 770 | 780 |
| NSQPAKYIPP | EGKPPKLDEF | QSARSLGHFE | VTILGLNHEI | AIDVAFLPMY | SPEDVQASQI |
| 790 | 800 | 810 | 820 | 830 | 840 |
| DTFLTCMNFS | CVYPPAAPLS | GRLPDPKAVA | GDIVKAAADL | DRVHIIGILD | ICNLGNNKVE |
| VCLQKIYTPE |