A5DTK7
Gene name |
MSS116 (LELG_00693) |
Protein name |
ATP-dependent RNA helicase MSS116, mitochondrial |
Names |
|
Species |
Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) (Yeast) (Saccharomyces elongisporus) |
KEGG Pathway |
lel:LELG_00693 |
EC number |
3.6.4.13: Acting on ATP; involved in cellular and subcellular movement |
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 A5DTK7
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-A5DTK7-F1 | Predicted | AlphaFoldDB |
No variants for A5DTK7
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for A5DTK7 | |||||
No associated diseases with A5DTK7
3 regional properties for A5DTK7
Functions
| Description | ||
|---|---|---|
| EC Number | 3.6.4.13 | Acting on ATP; involved in cellular and subcellular movement |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
1 GO annotations of cellular component
| Name | Definition |
|---|---|
| mitochondrial matrix | The gel-like material, with considerable fine structure, that lies in the matrix space, or lumen, of a mitochondrion. It contains the enzymes of the tricarboxylic acid cycle and, in some organisms, the enzymes concerned with fatty acid oxidation. |
4 GO annotations of molecular function
| Name | Definition |
|---|---|
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
| ATP hydrolysis activity | Catalysis of the reaction: ATP + H2O = ADP + H+ phosphate. ATP hydrolysis is used in some reactions as an energy source, for example to catalyze a reaction or drive transport against a concentration gradient. |
| RNA binding | Binding to an RNA molecule or a portion thereof. |
| RNA helicase activity | Unwinding of an RNA helix, driven by ATP hydrolysis. |
3 GO annotations of biological process
| Name | Definition |
|---|---|
| mRNA processing | Any process involved in the conversion of a primary mRNA transcript into one or more mature mRNA(s) prior to translation into polypeptide. |
| regulation of translation | Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of proteins by the translation of mRNA or circRNA. |
| RNA splicing | The process of removing sections of the primary RNA transcript to remove sequences not present in the mature form of the RNA and joining the remaining sections to form the mature form of the RNA. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MMIARFGKQV | LRKNVLVSNR | IHFPVISRGF | HNSFINKSDD | LKSPPIDITK | GQTEAKVETK |
| 70 | 80 | 90 | 100 | 110 | 120 |
| KDKFAGFGLD | LDELIGETAK | GSQVTEQTEL | TKSEEEEKKK | KNINTNTNKN | DRKSVPAISL |
| 130 | 140 | 150 | 160 | 170 | 180 |
| EDFNPSQFKD | FKNTGLIDDV | ILRALDRAHF | KDLTPIQQKS | IVPLLETERG | MVCRAKTGTG |
| 190 | 200 | 210 | 220 | 230 | 240 |
| KTLTFLIPTL | QSAVSRKIAS | GGRSSGVDTV | IIVPTRDLAL | QIYDEYQKVL | RGISGSRKPH |
| 250 | 260 | 270 | 280 | 290 | 300 |
| ISYVIGGMKN | SFNPRNPSEI | VIATPGRLEA | DLRSPLFASA | FTDIKYRVYD | EADRLLDVGF |
| 310 | 320 | 330 | 340 | 350 | 360 |
| EPTLDSIDRS | IKMIRSDDAE | PLKSLLFSAT | VDARLDQFAK | QHINKKYDYI | NTVPEDDPEV |
| 370 | 380 | 390 | 400 | 410 | 420 |
| HENIHQVMYK | CKDAIDKFGS | FFNYVNQLVK | DSPDMKMMVF | LPTQTAVEFL | YSYMSEACHK |
| 430 | 440 | 450 | 460 | 470 | 480 |
| HDVDIDIFHL | HGKRSASQRQ | RALSNFKRDD | SGILITTDVA | ARGIDVKGVT | HVVQLFPSSE |
| 490 | 500 | 510 | 520 | 530 | 540 |
| IADYVHKVGR | TGRAGKEGKA | VLFITQPEMA | YVRRLNSERG | VTFEQVHESS | EIDNSIDFFE |
| 550 | 560 | 570 | 580 | 590 | 600 |
| GMRPDEQVAN | DFFYTLMSFL | AQISSTYRLR | ADDLVAENVS | LYRAILQKPD | AKLSLRAASA |
| 610 | 620 | 630 | 640 | 650 | 660 |
| LIKRLNRDVV | REFFEQGRGG | NNGGYGGYGG | YGGSSYGRSG | GSNRYSGGGG | NRSEKRFSFA |
| 670 | 680 | 690 | |||
| GRGGNSGGHS | GRGRGGRSGY | SGGRSSQYSD | WE |