Q4FZF3
Gene name |
Ddx49 |
Protein name |
Probable ATP-dependent RNA helicase DDX49 |
Names |
DEAD box protein 49 |
Species |
Mus musculus (Mouse) |
KEGG Pathway |
mmu:234374 |
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 Q4FZF3
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-Q4FZF3-F1 | Predicted | AlphaFoldDB |
24 variants for Q4FZF3
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
rs3388991866 | 9 | L>* | No | EVA | |
rs3388939771 | 24 | Q>H | No | EVA | |
rs3388984466 | 26 | T>A | No | EVA | |
rs3388939737 | 40 | R>Q | No | EVA | |
rs3388991617 | 48 | T>K | No | EVA | |
rs3388963179 | 55 | A>V | No | EVA | |
rs3399231990 | 77 | T>S | No | EVA | |
rs3388991668 | 89 | Q>* | No | EVA | |
rs3388988198 | 99 | L>V | No | EVA | |
rs3388975278 | 115 | L>Q | No | EVA | |
rs3399309685 | 132 | A>V | No | EVA | |
rs49343197 | 135 | L>V | No | EVA | |
rs3388957114 | 148 | F>I | No | EVA | |
rs3388984678 | 160 | Q>* | No | EVA | |
rs248383026 | 176 | V>I | No | EVA | |
rs3388988236 | 195 | E>K | No | EVA | |
rs3388988277 | 206 | F>V | No | EVA | |
rs3412117927 | 225 | L>S | No | EVA | |
rs3388969275 | 235 | L>P | No | EVA | |
rs3399222083 | 243 | Q>K | No | EVA | |
rs3399209494 | 244 | D>E | No | EVA | |
rs3388988084 | 346 | G>E | No | EVA | |
rs260494366 | 452 | R>L | No | EVA | |
rs3388963105 | 459 | T>I | No | EVA |
No associated diseases with Q4FZF3
5 regional properties for Q4FZF3
Type | Name | Position | InterPro Accession |
---|---|---|---|
conserved_site | ATP-dependent RNA helicase DEAD-box, conserved site | 150 - 158 | IPR000629 |
domain | Helicase, C-terminal | 218 - 382 | IPR001650 |
domain | DEAD/DEAH box helicase domain | 26 - 196 | IPR011545 |
domain | Helicase superfamily 1/2, ATP-binding domain | 21 - 222 | IPR014001 |
domain | RNA helicase, DEAD-box type, Q motif | 2 - 30 | IPR014014 |
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 |
---|---|
nucleus | A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent. |
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 |
---|---|
positive regulation of cell growth | Any process that activates or increases the frequency, rate, extent or direction of cell growth. |
regulation of rRNA stability | Any process that modulates the propensity of rRNA molecules to degradation. Includes processes that both stabilize and destabilize rRNAs. |
rRNA processing | Any process involved in the conversion of a primary ribosomal RNA (rRNA) transcript into one or more mature rRNA molecules. |
14 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
Q9Y6V7 | DDX49 | Probable ATP-dependent RNA helicase DDX49 | Homo sapiens (Human) | PR |
Q8K363 | Ddx18 | ATP-dependent RNA helicase DDX18 | Mus musculus (Mouse) | PR |
Q8K4L0 | Ddx54 | ATP-dependent RNA helicase DDX54 | Mus musculus (Mouse) | PR |
Q9CWX9 | Ddx47 | Probable ATP-dependent RNA helicase DDX47 | Mus musculus (Mouse) | PR |
Q9CWT6 | Ddx28 | Probable ATP-dependent RNA helicase DDX28 | Mus musculus (Mouse) | PR |
Q91VR5 | Ddx1 | ATP-dependent RNA helicase DDX1 | Mus musculus (Mouse) | PR |
Q6ZPL9 | Ddx55 | ATP-dependent RNA helicase DDX55 | Mus musculus (Mouse) | PR |
Q9ESV0 | Ddx24 | ATP-dependent RNA helicase DDX24 | Mus musculus (Mouse) | PR |
P60843 | Eif4a1 | Eukaryotic initiation factor 4A-I | Mus musculus (Mouse) | PR |
P10630 | Eif4a2 | Eukaryotic initiation factor 4A-II | Mus musculus (Mouse) | PR |
Q569Z5 | Ddx46 | Probable ATP-dependent RNA helicase DDX46 | Mus musculus (Mouse) | PR |
Q8L4E9 | Os07g0633500 | DEAD-box ATP-dependent RNA helicase 36 | Oryza sativa subsp japonica (Rice) | PR |
Q9FZ92 | RH44 | Putative DEAD-box ATP-dependent RNA helicase 44 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9SA27 | RH36 | DEAD-box ATP-dependent RNA helicase 36 | Arabidopsis thaliana (Mouse-ear cress) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MAGFAEIGLS | SWLVEQCRQL | GLKQPTPVQL | GCIPAILEGR | DCLGCAKTGS | GKTAAFVLPI |
70 | 80 | 90 | 100 | 110 | 120 |
LQKLSEDPYG | IFCLVLTPTR | ELAYQIAEQF | RVLGKPLGLK | DCIIVGGMDM | VAQALELSRK |
130 | 140 | 150 | 160 | 170 | 180 |
PHVVIATPGR | LADHLRSSNT | FNMKKIQFLV | MDEADRLLEQ | GCTDFTTDLE | TILAAVPARR |
190 | 200 | 210 | 220 | 230 | 240 |
QTLLFSATLT | DTLKELQGLA | TNEPFFWEAQ | ATVRTVEQLD | QRYLLVPEKV | KDAYLVHLVQ |
250 | 260 | 270 | 280 | 290 | 300 |
TFQDQLEDCS | IIIFTNTCKT | CQILCMMLRK | FNFPTVALHS | MMKQKERFAA | LAKFKSSIYR |
310 | 320 | 330 | 340 | 350 | 360 |
ILIATDVASR | GLDIPTVQVV | INHNTPGLPK | IYIHRVGRTA | RAGRQGQAIT | LVTQYDIHLL |
370 | 380 | 390 | 400 | 410 | 420 |
HAIEEQIKQQ | LAELVVEEAE | VLQILTQVNV | VRRECEIKLE | ASHFDEKKEI | NKRKQMILEG |
430 | 440 | 450 | 460 | 470 | |
KDPDLEAKRK | AELAKIKQQN | RRFKEKVGQT | LRRQKAGSTV | RRSRPPRSRP | QEPAQAEAQD |