O74755
Gene name |
pst3 (SPBC1734.16c) |
Protein name |
Paired amphipathic helix protein pst3 |
Names |
SIN3 homolog 3 |
Species |
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) |
KEGG Pathway |
spo:SPBC1734.16c |
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
2 structures for O74755
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| 8I03 | EM | 320 A | B | 1-1154 | PDB |
| AF-O74755-F1 | Predicted | AlphaFoldDB |
No variants for O74755
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for O74755 | |||||
No associated diseases with O74755
4 regional properties for O74755
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| repeat | Paired amphipathic helix | 111 - 181 | IPR003822-1 |
| repeat | Paired amphipathic helix | 252 - 322 | IPR003822-2 |
| domain | Histone deacetylase interacting domain | 492 - 592 | IPR013194 |
| domain | Sin3, C-terminal | 885 - 1096 | IPR031693 |
8 GO annotations of cellular component
| Name | Definition |
|---|---|
| chromatin | The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome. |
| Clr6 histone deacetylase complex I'' | A histone deacetylase complex involved in chromatin organization. In Schizosaccharomyces pombe this complex consists of Clr6, Nts1, Mug165, and Png3. |
| cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
| histone deacetylase complex | A protein complex that possesses histone deacetylase activity. |
| 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. |
| Rpd3L complex | A histone deacetylase complex which deacetylates histones preferentially in promoter regions. Composed of a catalytic histone deacetylase subunit, an Sds-3 family protein, a SIN3 family co-repressor, a WD repeat protein, and a zf- PHD finger (Clr6, Sds3, Pst1, Prw1, Png2 in Schizosaccharomyces pombe; Rpd3p, Sin3p, Ume1p, Pho23p, Sap30p, Sds3p, Cti6p, Rxt2p, Rxt3p, Dep1p, Ume6p and Ash1p in Saccharomyces cerevisiae). |
| Rpd3L-Expanded complex | A protein complex that contains a histone deacetylase and is part of the chromatin remodeling machinery. In Saccharomyces cerevisiae this complex contains the Rpd3p, Sin3p, Ume1p, Pho23p, Sap30p, Sds3p, Cti6p, Rxt2p, Rxt3p, Dep1p, Ume6p, Ash1p, Dot6p, Snt1, Sif2p, Set3p, Hos2p, Tos4p and Tod6p proteins. |
| Sin3-type complex | Any of a number of evolutionarily conserved histone deacetylase complexes (HDACs) containing a core consisting of a paired amphipathic helix motif protein (e.g. Sin3p in S. cerevisiae, Pst1 in S. pombe or Sin3A in mammals) at least one class I histone deacetylase (e.g. Rpd3p in S. cerevisiae, Clr6 in S. pombe, or HDAC1 and HDAC2 in mammals), and at least one WD40 repeat protein (e.g. Ume1p in S. cerevisiae, Prw1 in S. pombe, or RbAp46 and RbAp48 in mammals). These complexes also contain a variable number of other proteins that direct histone binding, DNA binding, or add other functionality to the complex. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| transcription corepressor activity | A transcription coregulator activity that represses or decreases the transcription of specific gene sets via binding to a DNA-bound DNA-binding transcription factor, either on its own or as part of a complex. Corepressors often act by altering chromatin structure and modifications. For example, one class of transcription corepressors modifies chromatin structure through covalent modification of histones. A second class remodels the conformation of chromatin in an ATP-dependent fashion. A third class modulates interactions of DNA-bound DNA-binding transcription factors with other transcription coregulators. |
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. |
| histone deacetylation | The modification of histones by removal of acetyl groups. |
| 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. |
| regulation of DNA-templated transcription | Any process that modulates the frequency, rate or extent of cellular DNA-templated transcription. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MDVMNVPVDS | ERDNPGDKVE | TQSDKNHLPK | ASPSQSQSPV | NTSLHNGDGK | DNGVATEPVE |
| 70 | 80 | 90 | 100 | 110 | 120 |
| NKQILSERSV | TRDDYEKGKT | IVSSLALSSI | SGKDGSISSQ | NAEGLSSSSN | RPLDVNDALS |
| 130 | 140 | 150 | 160 | 170 | 180 |
| YLELVKYYFS | ERREIYNRFL | EIMRDFKSQA | LDTLGVINRV | SELFNGYPQL | IEGFNTFLPS |
| 190 | 200 | 210 | 220 | 230 | 240 |
| GYKIEVQLDS | SNTSVVRVGT | PMHPLPQQGV | QSTLPVAPSN | EDQRTMESTS | PTDSQPQPSA |
| 250 | 260 | 270 | 280 | 290 | 300 |
| PNLVSSTENE | KPRVDFNYAI | AYMNKVKARY | PPNSDTYMEF | LGVLRTYQKA | QKSIFEVRAR |
| 310 | 320 | 330 | 340 | 350 | 360 |
| VAEIFKDSPD | LLEEFKLFLP | DNVDSTEPST | PNVQKSPNRL | PPVGNFSLPP | SAPVREKRNR |
| 370 | 380 | 390 | 400 | 410 | 420 |
| PAHSAQISRS | ISKTSRMYRQ | TAEEPLNSYS | LHVYPQKITA | PTSPYAATQE | ELLAFTTIRQ |
| 430 | 440 | 450 | 460 | 470 | 480 |
| HLPDTLAFHK | FLELLHLYRE | KLLDKTELLN | SFSKLVRNDN | LTLWFSEFIR | WSDNPILVKN |
| 490 | 500 | 510 | 520 | 530 | 540 |
| EPVDERVYLP | ETFECISLTY | RKLPDSWKQD | KCSGRDDLDN | SVLNDDYISV | APKPSHVKNI |
| 550 | 560 | 570 | 580 | 590 | 600 |
| MHHENQYLQA | LQLVEDERYD | YDRVLNTTES | AIKILANFCE | PTIHEHLETA | LQELERSKRI |
| 610 | 620 | 630 | 640 | 650 | 660 |
| IKNALIIVYG | KEHANLALDT | LFKKLPTAAP | VLLKRIKTKD | QEWRRSKREW | SKIWRQIEKK |
| 670 | 680 | 690 | 700 | 710 | 720 |
| NAQAAFDDRY | CRIEGRDRRG | LSYSRILRDI | DDIYQRQKHR | IDGAKLGFQF | TQVLCDSLIF |
| 730 | 740 | 750 | 760 | 770 | 780 |
| LNILRLSDAQ | LTNSSFYSYA | DKGRISAVLK | ALLSQFFGIP | LPREALETNL | ASENIESVKK |
| 790 | 800 | 810 | 820 | 830 | 840 |
| HRDGLSKIFI | RPESADNSNN | TNVSFQTDET | QTEDETMSDI | HPDDVENHSK | SKFLGEESKN |
| 850 | 860 | 870 | 880 | 890 | 900 |
| IIGYNFFGNA | TMYVLFRLIC | VCYSRLEHIK | LFVESSTIYA | SSTGGYENIL | NICEKYLKGS |
| 910 | 920 | 930 | 940 | 950 | 960 |
| CSRLEFRKYL | QKFNNETCYM | ICSIERLLKV | IFYRIHEILL | DPKLGQLLLL | FESDGANSVT |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| TPREQMVYRN | HVESILAPES | KIFNMRWYPL | EKRLCIQQLL | PADLTMHDFE | NPAKAFMYYV |
| 1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
| DSYAISHITE | GVDLMQVKMP | FLRRSLQRIS | QQGYLAGRGS | GRLHSLFNEH | FCKSNLQLFF |
| 1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
| STDTYVIFFE | PNTENVYINS | YNLWVDQSSQ | SKKQNRTTNW | RRWLESDEGW | RKSKANTDIK |
| 1150 | |||||
| FFSETTLDQC | IEAM |