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
0 structures for Q89926
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|
No variants for Q89926
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q89926 | |||||
No associated diseases with Q89926
1 GO annotations of cellular component
| Name | Definition |
|---|---|
| virion component | Any constituent part of a virion, a complete fully infectious extracellular virus particle. |
4 GO annotations of molecular function
| Name | Definition |
|---|---|
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
| ATP-dependent chromatin remodeler activity | An activity, driven by ATP hydrolysis, that modulates the contacts between histones and DNA, resulting in a change in chromosome architecture within the nucleosomal array, leading to chromatin remodeling. |
| hydrolase activity | Catalysis of the hydrolysis of various bonds, e.g. C-O, C-N, C-C, phosphoric anhydride bonds, etc. |
| RNA helicase activity | Unwinding of an RNA helix, driven by ATP hydrolysis. |
No GO annotations of biological process
| Name | Definition |
|---|---|
| No GO annotations for biological process |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSCVHNNTSF | PVQIEAYLKE | VFEKYKELQE | SKDTSLTARF | ARVLKYYQFL | IYSAFSDPKF |
| 70 | 80 | 90 | 100 | 110 | 120 |
| GIGQGENTRG | LLIYHQMGMG | KTILSLSLAI | SLSHIYNPIL | IAPKSLHSNF | QQSLLKLIKL |
| 130 | 140 | 150 | 160 | 170 | 180 |
| LYPETTDHSK | ELQKISRRFR | FVSLDAYNMG | QQIIKAGGSL | NGCLLIVDEA | HNLFRGIINS |
| 190 | 200 | 210 | 220 | 230 | 240 |
| ANDKTNARQL | YNNIMQAKNI | RILFLTGTPC | SKDPFEMVPC | FNMLSGRILL | PLHYERFYTA |
| 250 | 260 | 270 | 280 | 290 | 300 |
| YVNKTTNSPL | NADKLLNRLV | GMISYAGNQN | ELNKLFPTEL | PLIIEKVEMS | PEQYRQYLLA |
| 310 | 320 | 330 | 340 | 350 | 360 |
| RDVENAEKHA | SSGMYEKMNT | AALCLPGSEQ | ESGSSYYVRS | RMISIFASEM | LTVKEDEKLS |
| 370 | 380 | 390 | 400 | 410 | 420 |
| EAVQQLPKEA | FTENSSPKIA | CMLKNIKTSP | GPVLIYSQFV | ELGLHVVARF | LEIEGYQCLQ |
| 430 | 440 | 450 | 460 | 470 | 480 |
| PLKVLEEGHN | TILLHKDGKD | LMVKNFAEDE | PTHTLVLSSK | ITRFTLITGK | ILSKERDMIQ |
| 490 | 500 | 510 | 520 | 530 | 540 |
| QLWNSPLNIH | GEVIKILLVS | KTGAEGLDLK | YGRQVHILEP | YWDKAREDQV | KARIIRIGSH |
| 550 | 560 | 570 | 580 | 590 | 600 |
| DALPPEEKTV | QPFLYIAVAN | QKMFYSIPEG | SQEQKTIDER | FHERGLEKSH | LNSAFRDLLK |
| 610 | 620 | 630 | 640 | 650 | 660 |
| RAAIECAFNG | ESGCLMCQPT | NALLFHENFE | RDLRLPNPCQ | PLVKTEVKAY | SISYEGKQFF |
| 670 | 680 | 690 | 700 | ||
| YQKNKEVGLG | YTFYEYNPII | KAYIEIKPSN | PLYIKLIKHV | QAGTTV |