O60059
Gene name |
SPBC56F2.08c |
Protein name |
Pumilio domain-containing protein C56F2.08c |
Names |
|
Species |
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) |
KEGG Pathway |
spo:SPBC56F2.08c |
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
4 structures for O60059
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| 6NWW | X-ray | 206 A | A/B/C/D | 1-79 | PDB |
| 6NX5 | X-ray | 155 A | A/B/C/D | 1-79 | PDB |
| 6NY5 | X-ray | 300 A | A/B | 109-485 | PDB |
| AF-O60059-F1 | Predicted | AlphaFoldDB |
No variants for O60059
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for O60059 | |||||
No associated diseases with O60059
No regional properties for O60059
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for O60059 | |||
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
| cytoplasmic stress granule | A dense aggregation in the cytosol composed of proteins and RNAs that appear when the cell is under stress. |
| P-body | A focus in the cytoplasm where mRNAs may become inactivated by decapping or some other mechanism. Protein and RNA localized to these foci are involved in mRNA degradation, nonsense-mediated mRNA decay (NMD), translational repression, and RNA-mediated gene silencing. |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| mRNA 3'-UTR AU-rich region binding | Binding to a region containing frequent adenine and uridine bases within the 3' untranslated region of a mRNA molecule or in pre-mRNA intron. The ARE-binding element consensus is UUAUUUAUU. ARE-binding proteins control the stability and/or translation of mRNAs. |
| 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. |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay | A major pathway of degradation of nuclear-transcribed mRNAs that proceeds through a series of ordered steps that includes poly(A) tail shortening and that can regulate mRNA stability. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MLYVSNLPVG | TSSSAIHALF | SAYGNVKDIW | MLSPDNSAIV | SYESLSSAIV | ARDALHNRPV |
| 70 | 80 | 90 | 100 | 110 | 120 |
| FENHGPVQVM | LAKPSSNYEP | GNITAAVSPP | ASTSSKDGVV | CSPTSTGASQ | LLKSRVDILE |
| 130 | 140 | 150 | 160 | 170 | 180 |
| VARQFEMRIN | LDIVDSMIAS | AIENNKVATE | ILPPVETLRS | RQFEASKLRE | IRKNIDSGFY |
| 190 | 200 | 210 | 220 | 230 | 240 |
| TQEEIEVIAR | SMLDDVAELS | SDYLGNTVVQ | KFFEYCSDPI | KEAMLERIAP | YLAAIGIHKN |
| 250 | 260 | 270 | 280 | 290 | 300 |
| GTWAAQKIID | VASTEKQMDL | IVKHLRPYTA | LLYFDQFGNY | VAQCCLRFKY | PKNTFLFEVM |
| 310 | 320 | 330 | 340 | 350 | 360 |
| ARHCCEIGQS | RFGARAIRAC | LENENATFEQ | QALVVASIII | NSHLLATNSN | GMLLLTWLLD |
| 370 | 380 | 390 | 400 | 410 | 420 |
| NSFFRNRHRL | LAIHLATHLH | TTCTHKLAST | LIFKLINNKQ | EPESRNLLLK | NLFFSEKDNV |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LTYILQDQAV | GPSFIHKVIT | YPSIGREFLA | QFHLVIKRVL | INIHAQPNAV | YCRLMEEVGM |
| 490 | 500 | 510 | 520 | 530 | 540 |
| TSKSISPSLS | GISAPSASVD | SSASRLARDF | GSLSLSSNSL | LGSLGGLEST | PAYPSYPSHI |
| 550 | 560 | 570 | 580 | 590 | 600 |
| PLGTASLPLK | GNLYQISRSD | DIKSGAPVLD | TSSLVNPTLA | KSASLNNSSL | LNPSSSLLRR |
| 610 | 620 | 630 | 640 | 650 | 660 |
| EVPAGKLTMP | AYPYTTQLMN | HTAGADYGLP | RLSSKLPQVF | PGNYPRLQQS | LFPRQGELRF |
| N |