Q9STN3
Gene name |
At4g08350 (T28D5.40) |
Protein name |
Putative transcription elongation factor SPT5 homolog 1 |
Names |
|
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT4G08350 |
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 Q9STN3
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9STN3-F1 | Predicted | AlphaFoldDB |
30 variants for Q9STN3
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| ENSVATH06566926 | 8 | D>G | No | 1000Genomes | |
| tmp_4_5286407_T_A | 19 | D>E | No | 1000Genomes | |
| tmp_4_5286536_A_C | 62 | E>D | No | 1000Genomes | |
| tmp_4_5286675_G_C | 109 | A>P | No | 1000Genomes | |
| ENSVATH00478548 | 123 | D>G | No | 1000Genomes | |
| ENSVATH14081668 | 127 | D>N | No | 1000Genomes | |
| ENSVATH02741322 | 180 | R>C | No | 1000Genomes | |
| tmp_4_5287269_G_A | 219 | A>T | No | 1000Genomes | |
| tmp_4_5287694_G_C | 295 | V>L | No | 1000Genomes | |
| tmp_4_5288455_G_A | 449 | V>I | No | 1000Genomes | |
| ENSVATH14081671 | 490 | T>A | No | 1000Genomes | |
| tmp_4_5288682_A_C | 492 | E>D | No | 1000Genomes | |
| ENSVATH14081672 | 494 | A>E | No | 1000Genomes | |
| ENSVATH06566948 | 595 | Q>E | No | 1000Genomes | |
| tmp_4_5289287_C_T | 597 | R>C | No | 1000Genomes | |
| ENSVATH06566949 | 616 | K>R | No | 1000Genomes | |
| ENSVATH06566951 | 637 | H>Q | No | 1000Genomes | |
| ENSVATH14081705 | 674 | N>T | No | 1000Genomes | |
| ENSVATH11265707 | 678 | P>S | No | 1000Genomes | |
| tmp_4_5289702_G_A | 679 | A>T | No | 1000Genomes | |
| ENSVATH06566976 | 853 | E>D | No | 1000Genomes | |
| ENSVATH14081725 | 855 | P>L | No | 1000Genomes | |
| ENSVATH06566977 | 872 | A>V | No | 1000Genomes | |
| ENSVATH06566978 | 903 | A>V | No | 1000Genomes | |
| ENSVATH06566980 | 924 | M>I | No | 1000Genomes | |
| tmp_4_5291629_C_T | 960 | S>L | No | 1000Genomes | |
| tmp_4_5291859_C_T,G | 971 | S>R | No | 1000Genomes | |
| ENSVATH00478578 | 971 | S>T | No | 1000Genomes | |
| ENSVATH14081731 | 982 | S>N | No | 1000Genomes | |
| tmp_4_5292068_C_G | 1041 | P>R | No | 1000Genomes |
No associated diseases with Q9STN3
17 regional properties for Q9STN3
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | NGN domain | 183 - 265 | IPR005100 |
| domain | KOW | 273 - 300 | IPR005824-1 |
| domain | KOW | 425 - 452 | IPR005824-2 |
| domain | KOW | 477 - 522 | IPR005824-3 |
| domain | KOW | 601 - 628 | IPR005824-4 |
| domain | KOW | 712 - 739 | IPR005824-5 |
| domain | KOW | 988 - 1015 | IPR005824-6 |
| conserved_site | Ribosomal protein L24/L26, conserved site | 429 - 446 | IPR005825 |
| domain | NusG-like, N-terminal | 181 - 268 | IPR006645 |
| domain | Spt5 transcription elongation factor, N-terminal | 90 - 177 | IPR022581 |
| domain | NGN domain, eukaryotic | 183 - 266 | IPR039385 |
| domain | Spt5, KOW domain repeat 1 | 277 - 314 | IPR041973 |
| domain | Spt5, KOW domain repeat 2 | 426 - 476 | IPR041975 |
| domain | Spt5, KOW domain repeat 3 | 477 - 527 | IPR041976 |
| domain | Spt5, KOW domain repeat 4 | 605 - 647 | IPR041977 |
| domain | Spt5, KOW domain repeat 5 | 711 - 758 | IPR041978 |
| domain | Spt5, KOW domain repeat 6 | 982 - 1039 | IPR041980 |
2 GO annotations of cellular component
| Name | Definition |
|---|---|
| DSIF complex | A heterodimeric protein complex formed of Spt4 and Spt5 proteins which is expressed in eukaryotes from yeast to man. DSIF is an inhibitory elongation factor that promotes RNA polymerase II transcriptional pausing, but can also stimulate transcriptional elongation under certain conditions, and may play a role in RNA processing via its physical association with mRNA capping enzymes. |
| ribosome | An intracellular organelle, about 200 A in diameter, consisting of RNA and protein. It is the site of protein biosynthesis resulting from translation of messenger RNA (mRNA). It consists of two subunits, one large and one small, each containing only protein and RNA. Both the ribosome and its subunits are characterized by their sedimentation coefficients, expressed in Svedberg units (symbol: S). Hence, the prokaryotic ribosome (70S) comprises a large (50S) subunit and a small (30S) subunit, while the eukaryotic ribosome (80S) comprises a large (60S) subunit and a small (40S) subunit. Two sites on the ribosomal large subunit are involved in translation, namely the aminoacyl site (A site) and peptidyl site (P site). Ribosomes from prokaryotes, eukaryotes, mitochondria, and chloroplasts have characteristically distinct ribosomal proteins. |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| mRNA binding | Binding to messenger RNA (mRNA), an intermediate molecule between DNA and protein. mRNA includes UTR and coding sequences, but does not contain introns. |
| structural constituent of ribosome | The action of a molecule that contributes to the structural integrity of the ribosome. |
4 GO annotations of biological process
| Name | Definition |
|---|---|
| regulation of DNA-templated transcription elongation | Any process that modulates the frequency, rate or extent of transcription elongation, the extension of an RNA molecule after transcription initiation and promoter clearance by the addition of ribonucleotides catalyzed by a DNA-dependent RNA polymerase. |
| regulation of transcription by RNA polymerase II | Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II. |
| transcription elongation by RNA polymerase II promoter | The extension of an RNA molecule after transcription initiation and promoter clearance at an RNA polymerase II promoter by the addition of ribonucleotides catalyzed by RNA polymerase II. |
| translation | The cellular metabolic process in which a protein is formed, using the sequence of a mature mRNA or circRNA molecule to specify the sequence of amino acids in a polypeptide chain. Translation is mediated by the ribosome, and begins with the formation of a ternary complex between aminoacylated initiator methionine tRNA, GTP, and initiation factor 2, which subsequently associates with the small subunit of the ribosome and an mRNA or circRNA. Translation ends with the release of a polypeptide chain from the ribosome. |
3 homologous proteins in AiPD
| 10 | 20 | 30 | 40 | 50 | 60 |
| MPRSRDEDDE | LDGDYEALDL | EEEEEEDEEE | EEERGRGGGG | SRRKRGRSNF | IDDYAEEDSQ |
| 70 | 80 | 90 | 100 | 110 | 120 |
| EEDDDDEDYG | SSRGGKGAAS | KRKKPSASIF | LDREAHQVDD | EDEEEEDEAE | DDFIVDNGTD |
| 130 | 140 | 150 | 160 | 170 | 180 |
| LPDERGDRRY | ERRFLPRDEN | DEDVEDLERR | IQERFSSRHH | EEYDEEATEV | EQQALLPSVR |
| 190 | 200 | 210 | 220 | 230 | 240 |
| DPKLWMVKCA | IGREREVAVC | LMQKFIDRGA | DLQIRSVVAL | DHLKNFIYVE | ADKEAHVKEA |
| 250 | 260 | 270 | 280 | 290 | 300 |
| IKGMRNIYAN | QKILLVPIRE | MTDVLSVESK | AIDLSRDTWV | RMKIGTYKGD | LAKVVDVDNV |
| 310 | 320 | 330 | 340 | 350 | 360 |
| RQRVTVKLIP | RIDLQALASK | LDGREVSKKK | AFVPPPRFMN | IDEARELHIR | VERRRDHMTG |
| 370 | 380 | 390 | 400 | 410 | 420 |
| DYFENIGGML | FKDGFHYKQV | SLKSITVQNV | TPTFDELEKF | NKPSENGEGD | FGGLSTLFAN |
| 430 | 440 | 450 | 460 | 470 | 480 |
| RKKGHFMKGD | AVIVIKGDLK | NLKGWVEKVD | EENVLIRSEV | KGLPDPLAVN | ERELCKYFEP |
| 490 | 500 | 510 | 520 | 530 | 540 |
| GNHVKVVSGT | HEGATGMVVK | VDQHVLIILS | DTTKEHVRVF | ADHVVESSEV | TTGVTKIGDY |
| 550 | 560 | 570 | 580 | 590 | 600 |
| ELHDLVLLDN | LSFGVIIRLE | NEAFQVLKGV | PDRPEVALVK | LREIKCKLEK | KINVQDRYKN |
| 610 | 620 | 630 | 640 | 650 | 660 |
| VIAVKDDVRV | IEGPSKGKQG | PVKHIYKGVL | FIYDRHHLEH | AGFICAKCTS | CIVVGGSRSG |
| 670 | 680 | 690 | 700 | 710 | 720 |
| ANRNGGDSLS | RYGNFKAPAP | VPSSPGRFQR | GRGGGYNNSG | GRHGGGRGRG | DDSLLGTTVK |
| 730 | 740 | 750 | 760 | 770 | 780 |
| IRLGPFKGYR | GPVVEVKGNS | VRVELEMKIV | TVDRGAISDN | VATTPFRDTS | RYSMGSETPM |
| 790 | 800 | 810 | 820 | 830 | 840 |
| HPSRTPLHPY | MTPMRDSGAT | PIHDGMRTPM | RDRAWNPYTP | MSPPRDNWED | GNPGSWGTSP |
| 850 | 860 | 870 | 880 | 890 | 900 |
| QYQPGSPPSR | AYEAPTPGSG | WASTPGGSYS | DAGTPRDHGS | AYANAPSPYL | PSTPGQPMTP |
| 910 | 920 | 930 | 940 | 950 | 960 |
| SSASYLPGTP | GGQPMTPGTG | LDVMSPVIGG | DAEAWFMPDI | LVDIHKAGED | TDVGVIRDVS |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| DGTCKVSLGS | SGEGDTIMAL | PSELEIIPPR | KSDRVKIVGG | QYRGSTGKLI | GIDGSDGIVK |
| 1030 | 1040 | ||||
| IDDNLDVKIL | DLALLAKFVQ | P |