Q5Z6G5
Gene name |
Os06g0697200 (LOC_Os06g48210, OsJ_22496, P0028E05.25) |
Protein name |
DEAD-box ATP-dependent RNA helicase 35B |
Names |
|
Species |
Oryza sativa subsp japonica (Rice) |
KEGG Pathway |
osa:4341945 |
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 Q5Z6G5
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-Q5Z6G5-F1 | Predicted | AlphaFoldDB |
No variants for Q5Z6G5
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
No variants for Q5Z6G5 |
No associated diseases with Q5Z6G5
5 regional properties for Q5Z6G5
Type | Name | Position | InterPro Accession |
---|---|---|---|
domain | Helicase, C-terminal | 399 - 559 | IPR001650 |
domain | DEAD/DEAH box helicase domain | 197 - 376 | IPR011545 |
domain | Helicase superfamily 1/2, ATP-binding domain | 192 - 403 | IPR014001 |
domain | RNA helicase, DEAD-box type, Q motif | 173 - 201 | IPR014014 |
domain | DDX41, DEAD-box helicase domain | 184 - 389 | IPR044113 |
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 |
---|---|
spliceosomal complex | Any of a series of ribonucleoprotein complexes that contain snRNA(s) and small nuclear ribonucleoproteins (snRNPs), and are formed sequentially during the spliceosomal splicing of one or more substrate RNAs, and which also contain the RNA substrate(s) from the initial target RNAs of splicing, the splicing intermediate RNA(s), to the final RNA products. During cis-splicing, the initial target RNA is a single, contiguous RNA transcript, whether mRNA, snoRNA, etc., and the released products are a spliced RNA and an excised intron, generally as a lariat structure. During trans-splicing, there are two initial substrate RNAs, the spliced leader RNA and a pre-mRNA. |
5 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. |
metal ion binding | Binding to a metal ion. |
RNA binding | Binding to an RNA molecule or a portion thereof. |
RNA helicase activity | Unwinding of an RNA helix, driven by ATP hydrolysis. |
1 GO annotations of biological process
Name | Definition |
---|---|
mRNA splicing, via spliceosome | The joining together of exons from one or more primary transcripts of messenger RNA (mRNA) and the excision of intron sequences, via a spliceosomal mechanism, so that mRNA consisting only of the joined exons is produced. |
17 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
Q9V3C0 | abs | ATP-dependent RNA helicase abstrakt | Drosophila melanogaster (Fruit fly) | PR |
Q9UJV9 | DDX41 | Probable ATP-dependent RNA helicase DDX41 | Homo sapiens (Human) | PR |
Q91VN6 | Ddx41 | Probable ATP-dependent RNA helicase DDX41 | Mus musculus (Mouse) | PR |
Q10I26 | EIF4A3B | Eukaryotic initiation factor 4A-III homolog B | Oryza sativa subsp japonica (Rice) | PR |
Q5VNM3 | EIF4A3A | Eukaryotic initiation factor 4A-III homolog A | Oryza sativa subsp japonica (Rice) | PR |
Q2R1M8 | Os11g0599500 | DEAD-box ATP-dependent RNA helicase 52C | Oryza sativa subsp. japonica (Rice) | SS |
Q6Z4K6 | PL10B | DEAD-box ATP-dependent RNA helicase 52B | Oryza sativa subsp. japonica (Rice) | SS |
Q75HJ0 | PL10A | DEAD-box ATP-dependent RNA helicase 37 | Oryza sativa subsp. japonica (Rice) | SS |
Q10RI7 | Os03g0158200 | DEAD-box ATP-dependent RNA helicase 38 | Oryza sativa subsp japonica (Rice) | PR |
Q5QMN3 | Os01g0197200 | DEAD-box ATP-dependent RNA helicase 20 | Oryza sativa subsp japonica (Rice) | PR |
Q0E2Z7 | Os02g0201900 | DEAD-box ATP-dependent RNA helicase 41 | Oryza sativa subsp japonica (Rice) | PR |
Q5JK84 | AIP2 | DEAD-box ATP-dependent RNA helicase 15 | Oryza sativa subsp japonica (Rice) | PR |
Q0JM17 | AIP1 | DEAD-box ATP-dependent RNA helicase 56 | Oryza sativa subsp japonica (Rice) | PR |
Q0E3X4 | Os02g0150100 | DEAD-box ATP-dependent RNA helicase 35A | Oryza sativa subsp japonica (Rice) | PR |
Q5N7W4 | Os01g0911100 | DEAD-box ATP-dependent RNA helicase 30 | Oryza sativa subsp japonica (Rice) | PR |
Q9LU46 | RH35 | DEAD-box ATP-dependent RNA helicase 35 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9SZB4 | RH43 | Putative DEAD-box ATP-dependent RNA helicase 43 | Arabidopsis thaliana (Mouse-ear cress) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MAAAAAAAAA | GDSPRRGTPD | SDEEDYEEYV | PVAKRRAMEA | ERLRRATKPP | TTNAVAVAAP |
70 | 80 | 90 | 100 | 110 | 120 |
PPPPRSTSSP | AVGEVAVKTS | LLVKATKLKR | EAPEVTPAER | LLQQEREMIE | HLSDRKALMP |
130 | 140 | 150 | 160 | 170 | 180 |
VGEIAKGISY | SEPITTGWRP | PLRLRRMPRS | RADALRRSWH | ILVDGDDVPP | PSRSFGDLRL |
190 | 200 | 210 | 220 | 230 | 240 |
PEPILRALRG | KGIEKPTPIQ | VQGLPVALSG | RDMIGIAFTG | SGKTLVFVLP | LIMAALQEEI |
250 | 260 | 270 | 280 | 290 | 300 |
LMPIVPGEGP | FGLIVCPSRE | LARQTHEVIE | MFLAPLMEAG | YPEIRPLLCI | GGVDMRTQME |
310 | 320 | 330 | 340 | 350 | 360 |
VVKKGVHIVV | ATPGRLKDLL | SKKKMNLDNC | RYLTLDEADR | LVDLGFEDDI | REVFDHFKAQ |
370 | 380 | 390 | 400 | 410 | 420 |
RQTLLFSATM | PEKIQNFAKS | ALVKPIIVNV | GRAGAANLDV | IQEVEYVKEE | ARIIYLLECL |
430 | 440 | 450 | 460 | 470 | 480 |
QKTPPPVLVF | CEHKADVDYI | QEFLLLKGVE | AVAIHGGKDD | EERKDAFKSF | KASEKDVLVA |
490 | 500 | 510 | 520 | 530 | 540 |
TDVASKGLDI | PDIQHVINYD | MPAEIENYVH | RIGRTGRRGK | TGVATTFINK | NQTETTLLDL |
550 | 560 | 570 | 580 | 590 | 600 |
KQLLIESKQR | LPPILADLDD | PQEDDKVAIA | QQSGVKGCAF | CGGLGHRIEA | CPKQQLQNSV |
610 | |||||
TLARARSDYF | GGGGYRGEI |