Q9UTN6
Gene name |
snf21 (SPAC1250.01, SPAC29A4.21) |
Protein name |
Chromatin structure-remodeling complex subunit snf21 |
Names |
ATP-dependent helicase snf21, RSC complex subunit snf21 |
Species |
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) |
KEGG Pathway |
spo:SPAC1250.01 |
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 Q9UTN6
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9UTN6-F1 | Predicted | AlphaFoldDB |
11 variants for Q9UTN6
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| I_5103974_T_A | 15 | T>S | No | Jeffares_SNPs | |
| I_5103872_T_A | 35 | Y>F | No | Jeffares_SNPs | |
| I_5103582_C_T | 132 | G>S | No | Jeffares_SNPs | |
| I_5103513_C_T | 155 | D>N | No | Jeffares_SNPs | |
| I_5103413_A_G | 188 | L>S | No | Jeffares_SNPs | |
| I_5103365_A_G | 204 | L>S | No | Jeffares_SNPs | |
| I_5103176_T_C | 267 | K>R | No | Jeffares_SNPs | |
| I_5102751_G_T | 409 | P>T | No | Jeffares_SNPs | |
| I_5101126_C_A | 950 | R>S | No | Jeffares_SNPs | |
| I_5100502_G_T | 1158 | N>K | No | Jeffares_SNPs | |
| I_5100491_G_T | 1162 | T>K | No | Jeffares_SNPs |
No associated diseases with Q9UTN6
No regional properties for Q9UTN6
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for Q9UTN6 | |||
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| chromatin | The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome. |
| 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. |
| RSC-type complex | A SWI/SNF-type complex that contains a bromodomain containing-protein, such as yeast Rsc1 or Rsc4 or mammalian PB1/BAF180. The RSC complex is generally recruited to RNA polymerase III promoters and is specifically recruited to RNA polymerase II promoters by transcriptional activators and repressors; it is also involved in non-homologous end joining. |
8 GO annotations of molecular function
| Name | Definition |
|---|---|
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
| ATP-dependent activity, acting on DNA | Catalytic activity that acts to modify DNA, driven by ATP hydrolysis. |
| chromatin-protein adaptor | The binding activity of a molecule that brings together a protein or a protein complex with a nucleosome, to establish or maintain the chromatin localization of the protein, or protein complex. |
| DNA binding | Any molecular function by which a gene product interacts selectively and non-covalently with DNA (deoxyribonucleic acid). |
| helicase activity | Catalysis of the reaction: ATP + H2O = ADP + phosphate, to drive the unwinding of a DNA or RNA helix. |
| 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. |
| histone octamer slider activity | A chromatin remodeler activity that slides core histone octamers along chromosomal DNA. |
| hydrolase activity | Catalysis of the hydrolysis of various bonds, e.g. C-O, C-N, C-C, phosphoric anhydride bonds, etc. |
5 GO annotations of biological process
| Name | Definition |
|---|---|
| chromatin remodeling | A dynamic process of chromatin reorganization resulting in changes to chromatin structure. These changes allow DNA metabolic processes such as transcriptional regulation, DNA recombination, DNA repair, and DNA replication. |
| double-strand break repair via nonhomologous end joining | The repair of a double-strand break in DNA in which the two broken ends are rejoined with little or no sequence complementarity. Information at the DNA ends may be lost due to the modification of broken DNA ends. This term covers instances of separate pathways, called classical (or canonical) and alternative nonhomologous end joining (C-NHEJ and A-NHEJ). These in turn may further branch into sub-pathways, but evidence is still unclear. |
| mitotic cohesin loading | The protein localization to chromatin by which a cohesin ring complex is topologically linked to DNA as part of the mitotic cell cycle. |
| positive regulation of transcription by RNA polymerase II | Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase II promoter. |
| regulation of transcription by RNA polymerase II | Any process that modulates the frequency, rate or extent of transcription mediated 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 |
| MRAEKQYTRN | EVEETIVRWK | KLKESGATEH | DNTEYAQLCD | VLRSAQSEIE | ARRDLKGHIK |
| 70 | 80 | 90 | 100 | 110 | 120 |
| RCFSSVDKNT | EKLILKQQVL | AYKKLSQNLP | APDDCILSVL | LRLSKDEQLL | QSIVKQPLQN |
| 130 | 140 | 150 | 160 | 170 | 180 |
| SKVDGKVRRD | FGSCQITPSA | KQQRKYLQYQ | ISEDDAIKNR | MFRRMSDLES | YPAVMRDVAE |
| 190 | 200 | 210 | 220 | 230 | 240 |
| LKDDNERLNL | DTIKRNALVE | LKKLRLIKQQ | ESLRHQVMHC | QPHLRTIVNA | VERMSCRRPK |
| 250 | 260 | 270 | 280 | 290 | 300 |
| LVPQATRLTE | VLERQQRSDR | ERRLKQKQCD | YLQTVCAHGR | EINVRTKNAQ | ARAQKANRAV |
| 310 | 320 | 330 | 340 | 350 | 360 |
| LAYHSHIEKE | EQRRAERNAK | QRLQALKEND | EEAYLKLIDQ | AKDTRITHLL | RQTDHYLDSL |
| 370 | 380 | 390 | 400 | 410 | 420 |
| AAAVKVQQSQ | FGESAYDEDM | DRRMNPEDDR | KIDYYNVAHN | IREVVTEQPS | ILVGGKLKEY |
| 430 | 440 | 450 | 460 | 470 | 480 |
| QLRGLQWMIS | LYNNHLNGIL | ADEMGLGKTI | QTISLITHLI | EKKRQNGPFL | VIVPLSTLTN |
| 490 | 500 | 510 | 520 | 530 | 540 |
| WTMEFERWAP | SIVKIVYKGP | PQVRKALHPQ | VRHSNFQVLL | TTYEYIIKDR | PLLSRIKWIY |
| 550 | 560 | 570 | 580 | 590 | 600 |
| MIIDEGHRMK | NTQSKLTNTL | TTYYSSRYRL | ILTGTPLQNN | LPELWALLNF | VLPRIFNSIK |
| 610 | 620 | 630 | 640 | 650 | 660 |
| SFDEWFNTPF | ANTGGQDKME | LTEEESLLVI | RRLHKVLRPF | LLRRLKKDVE | AELPDKVEKV |
| 670 | 680 | 690 | 700 | 710 | 720 |
| IRCQMSGLQQ | KLYYQMKKHG | MLYVEDAKRG | KTGIKGLQNT | VMQLKKICNH | PFVFEDVERS |
| 730 | 740 | 750 | 760 | 770 | 780 |
| IDPTGFNYDM | LWRVSGKFEL | LDRILPKLFR | SGHRILMFFQ | MTQIMNIMED | YLHYRQWRYL |
| 790 | 800 | 810 | 820 | 830 | 840 |
| RLDGSTKADD | RSKLLGVFND | PTAEVNLFLL | STRAGGLGLN | LQTADTVIIF | DSDWNPHQDL |
| 850 | 860 | 870 | 880 | 890 | 900 |
| QAQDRAHRIG | QTKEVRIYRL | ITEKSVEENI | LARAQYKLDI | DGKVIQAGKF | DNKSTPEERE |
| 910 | 920 | 930 | 940 | 950 | 960 |
| AFLRSLLENE | NGEEENDEKG | ELDDDELNEI | LARGDDELRL | FKQMTEDLER | ESPYGKNKEK |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| ERLIQVSELP | EFYQREEPEK | TTDLLQEEPL | GRGARRRTPV | VYDEAVRDAQ | WMAEMDMESE |
| 1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
| ARPTRGRPKR | NIASVDETPA | LTLNGKPKKK | RGPAPDTLTS | EHRSLLRRVC | LEIYKAVNEL |
| 1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
| EDDNGRPLNK | LFLELPSKKL | YPDYYMIIKS | PIALDAIRKH | INGTFYKTLE | AMKSDLMTMF |
| 1150 | 1160 | 1170 | 1180 | 1190 | |
| NNARTYNEEG | SFVYEDANKM | QTAMETKIEE | LEEDGTLATL | RGMEAEATSQ | LEDRIENEA |