Q8NIV6
Gene name |
spt-6 (NCU04611) |
Protein name |
Transcription elongation factor spt-6 |
Names |
Chromatin elongation factor spt-6 |
Species |
Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) |
KEGG Pathway |
ncr:NCU04611 |
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 Q8NIV6
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q8NIV6-F1 | Predicted | AlphaFoldDB |
No variants for Q8NIV6
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q8NIV6 | |||||
No associated diseases with Q8NIV6
10 regional properties for Q8NIV6
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | S1 domain | 1093 - 1161 | IPR003029 |
| domain | RNA-binding domain, S1 | 1092 - 1161 | IPR022967 |
| domain | Spt6 acidic, N-terminal domain | 40 - 125 | IPR028083 |
| domain | Helix-turn-helix DNA-binding domain of Spt6 | 282 - 405 | IPR028088 |
| domain | Transcription elongation factor Spt6, YqgF domain | 699 - 854 | IPR028231 |
| domain | Transcription elongation factor Spt6, helix-hairpin-helix motif | 856 - 965 | IPR032706 |
| domain | Spt6, SH2 domain, C terminus | 1301 - 1390 | IPR035018 |
| domain | Spt6, SH2 domain, N terminus | 1207 - 1291 | IPR035019 |
| domain | Spt6, SH2 domain | 1180 - 1388 | IPR035420 |
| domain | HHH domain 9 | 974 - 1010 | IPR041692 |
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| euchromatin | A dispersed and relatively uncompacted form of chromatin that is in a transcription-competent conformation. |
| pericentric heterochromatin | Heterochromatin that is located adjacent to the CENP-A rich centromere 'central core' and characterized by methylated H3 histone at lysine 9 (H3K9me2/H3K9me3). |
| transcription elongation factor complex | Any protein complex that interacts with RNA polymerase II to increase (positive transcription elongation factor) or reduce (negative transcription elongation factor) the rate of transcription elongation. |
4 GO annotations of molecular function
| Name | Definition |
|---|---|
| DNA binding | Any molecular function by which a gene product interacts selectively and non-covalently with DNA (deoxyribonucleic acid). |
| histone binding | Binding to a histone, any of a group of water-soluble proteins found in association with the DNA of eukaryotic or archaeal chromosomes. They are involved in the condensation and coiling of chromosomes during cell division and have also been implicated in gene regulation and DNA replication. They may be chemically modified (methylated, acetlyated and others) to regulate gene transcription. |
| nucleosome binding | Binding to a nucleosome, a complex comprised of DNA wound around a multisubunit core and associated proteins, which forms the primary packing unit of DNA into higher order structures. |
| transcription antitermination factor activity, DNA binding | Binds to DNA, typically within region of the promoter and transcribed region, to promote readthrough of a transcription termination site and thus extending the length of the RNA transcript produced. Examples of antitermination factors which bind DNA include the lambda Q protein. |
13 GO annotations of biological process
| Name | Definition |
|---|---|
| carbon catabolite repression of transcription from RNA polymerase II promoter by glucose | A transcription regulation process in which the presence of glucose leads to a decrease in the frequency, rate, or extent of transcription of specific RNA polymerase II-transcribed genes involved in the metabolism of other carbon sources. Carbon catabolite repression is a mechanism of genetic regulation which the accumulation of catabolites of one substance in the cell represses the formation of enzymes that contribute to the catabolism of other substances. |
| co-transcriptional chromatin reassembly | The reestablishment of chromatin structure that was disrupted upon passage of RNA polymerase II during transcription elongation. This process prevents cryptic intragenic transcription initiation. |
| mRNA transcription by RNA polymerase II | The cellular synthesis of messenger RNA (mRNA) from a DNA template by RNA polymerase II, originating at an RNA polymerase II promoter. |
| negative regulation of transcription by RNA polymerase II | Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II. |
| nucleosome assembly | The aggregation, arrangement and bonding together of a nucleosome, the beadlike structural units of eukaryotic chromatin composed of histones and DNA. |
| nucleosome organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of one or more nucleosomes. |
| poly(A)+ mRNA export from nucleus | The directed movement of poly(A)+ mRNA out of the nucleus into the cytoplasm. |
| positive regulation of transcription elongation by RNA polymerase II | Any process that activates or increases 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 RNA polymerase II. |
| positive regulation of transcription involved in G1/S transition of mitotic cell cycle | Any process that activates or increases transcription as part of the G1/S transition of the mitotic cell cycle. |
| regulation of histone H3-K36 methylation | Any process that modulates the frequency, rate or extent of the covalent addition of a methyl group to the lysine at position 36 of histone H3. |
| regulation of mRNA 3'-end processing | Any process that modulates the frequency, rate or extent of mRNA 3'-end processing, any process involved in forming the mature 3' end of an mRNA molecule. |
| regulation of transcriptional start site selection at RNA polymerase II promoter | Any process that modulates the rate, frequency or extent of a process involved in the selection of the specific location within the template strand of an RNA polymerase II promoter for hybridization of the cognate ribonucleotides and formation of first phosphodiester bond within the nascent transcript. |
| 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. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSNSMRDLID | GEAELDDEED | DESFDEEAGD | RPRRRPNIDD | SSEEEEDDED | EEEARKIREG |
| 70 | 80 | 90 | 100 | 110 | 120 |
| FIVDEDEEDE | AEDSDARERR | RRKKRRRERE | EEEQLDEEDL | DLIGEAIPEW | ERKPQPQRLK |
| 130 | 140 | 150 | 160 | 170 | 180 |
| RGHRDDHRPT | ERRGLAEIFS | DEDEEHDDRG | YGRPSGRAQA | DEFDDFIEDD | YPEDDEERRH |
| 190 | 200 | 210 | 220 | 230 | 240 |
| REEDEEVARP | KDRGLNIDTT | GLDKDALEDM | DAIFGNGEDY | EWALQLEEEQ | EHAERTKEDI |
| 250 | 260 | 270 | 280 | 290 | 300 |
| ELQDVFEPSQ | LKEKLLTDED | NRIRFNDEPE | RFQLDRKAFK | NLQMTSDQFK | EEARWISNLM |
| 310 | 320 | 330 | 340 | 350 | 360 |
| LPSKNLSSEL | HGPFNKAVGK | VLEFFVIDGV | EVPYVFQHRR | DYLIHAKKMR | NPNRRDDPDA |
| 370 | 380 | 390 | 400 | 410 | 420 |
| PEYTVDAEKL | LTQDDLWKVL | DLDIRFRSFL | EKRNALEQTY | DKLKEKTRDD | ILEEMIRQAQ |
| 430 | 440 | 450 | 460 | 470 | 480 |
| SIEELQDLQD | YLNFQYSAEL | KDLAANDNSA | QREIKRAGGR | TAQFERIRRS | NAYKFVQALG |
| 490 | 500 | 510 | 520 | 530 | 540 |
| ITPDRLAKNI | LRESSKVTSE | DDSRLPDDLA | DTLVDADFPT | GELVINAARQ | MLAEEMFASP |
| 550 | 560 | 570 | 580 | 590 | 600 |
| RMRKHFRKNF | YGMGIVSCRR | TDKGLRKIDE | ANPYYEVKYL | KNMSIADLAV | RPELFLKMMK |
| 610 | 620 | 630 | 640 | 650 | 660 |
| AEEEGLIEIK | VSLENDREFR | QQLFSDFASE | NFSELADKWN | AERQKVIDLA | FDKLVKVIVK |
| 670 | 680 | 690 | 700 | 710 | 720 |
| GVKDSLRTAC | QDELLKTCRE | LYFKRLDQAP | YKPKGMVIGT | TPRVLTLSNG | MGDPNREPVS |
| 730 | 740 | 750 | 760 | 770 | 780 |
| WVSMDEDGRI | LEHGTFTNLA | RDESQREALA | ELVRRRQPDV | IGISGFSADT | HRLIKDVEGL |
| 790 | 800 | 810 | 820 | 830 | 840 |
| VSEKGLVGPE | YDDPETNEYR | SDLLEVIVIN | DEVARLYKDS | PRAVADHPSL | NPMTRYCIAL |
| 850 | 860 | 870 | 880 | 890 | 900 |
| ARYMQNPMKE | YAALGKDVTS | LQIHPYQQYL | PQAKLLKHLE | TAMVDMVNLV | GVDINVAMQD |
| 910 | 920 | 930 | 940 | 950 | 960 |
| ANTAHLLPYV | AGLGPRKAQL | LIKGINKNGG | VVTSRDELVG | DPERHKLPVL | GPRVWNNCAS |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| FLFIEYEPTN | PESDPLDNTR | IHPEDYDLAR | KVAADALGLD | EEDVKAETDE | NGAGAIVRKL |
| 1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
| FKDDEQDKVN | ELILEEYAEQ | LEREYQQRKR | ATLETIRAEL | QVPYEELRKK | FESLTVDQVF |
| 1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
| TMLTGENRDS | LCEGMIVAAN | VRVVKDDFAI | VKLDCGIEGR | IESHDVSYRH | SIKDVLHVGQ |
| 1150 | 1160 | 1170 | 1180 | 1190 | 1200 |
| VVQAKLIDLN | RKEFVSKLSM | RDEEMRRPFR | RHFDHGRDQW | DYRKEDEDRE | ELREKDKSTG |
| 1210 | 1220 | 1230 | 1240 | 1250 | 1260 |
| RAQRVVNHPL | FKPFNSTQAE | EYLGSQPSGE | VVIRPSSKGN | DHLAVTWKVA | DGVFQHVDVL |
| 1270 | 1280 | 1290 | 1300 | 1310 | 1320 |
| ELQKENEFAV | GRVLRVGKYT | YQDLDELIVD | HVKAMAKKVD | ELMQCDKFQK | GSRNETEKWL |
| 1330 | 1340 | 1350 | 1360 | 1370 | 1380 |
| TTYMDANPNR | STYAFCIDTK | HPGYFFLCFK | ASRNSRVNAW | PVRVIPHAFE | LMKSQYPDVR |
| 1390 | 1400 | ||||
| ALCNGFKLRY | QSEMLKQQSG | GR |