Q24311
Gene name |
Cul1 (cul-1, lin19, CG1877) |
Protein name |
Cullin homolog 1 |
Names |
Lin-19 homolog protein |
Species |
Drosophila melanogaster (Fruit fly) |
KEGG Pathway |
dme:Dmel_CG1877 |
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 Q24311
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q24311-F1 | Predicted | AlphaFoldDB |
No variants for Q24311
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q24311 | |||||
No associated diseases with Q24311
No regional properties for Q24311
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for Q24311 | |||
4 GO annotations of cellular component
| Name | Definition |
|---|---|
| cullin-RING ubiquitin ligase complex | Any ubiquitin ligase complex in which the catalytic core consists of a member of the cullin family and a RING domain protein; the core is associated with one or more additional proteins that confer substrate specificity. |
| cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
| 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. |
| SCF ubiquitin ligase complex | A ubiquitin ligase complex in which a cullin from the Cul1 subfamily and a RING domain protein form the catalytic core; substrate specificity is conferred by a Skp1 adaptor and an F-box protein. SCF complexes are involved in targeting proteins for degradation by the proteasome. The best characterized complexes are those from yeast and mammals (with core subunits named Cdc53/Cul1, Rbx1/Hrt1/Roc1). |
3 GO annotations of molecular function
| Name | Definition |
|---|---|
| molecular adaptor activity | The binding activity of a molecule that brings together two or more molecules through a selective, non-covalent, often stoichiometric interaction, permitting those molecules to function in a coordinated way. |
| protein-macromolecule adaptor activity | The binding activity of a protein that brings together two or more macromolecules in contact, permitting those molecules to function in a coordinated way. The adaptor can bring together two proteins, or a protein and another macromolecule such as a lipid or a nucleic acid. |
| ubiquitin protein ligase binding | Binding to a ubiquitin protein ligase enzyme, any of the E3 proteins. |
17 GO annotations of biological process
| Name | Definition |
|---|---|
| negative regulation of antimicrobial peptide production | Any process that stops, prevents, or reduces the frequency, rate, or extent of antimicrobial peptide production. |
| negative regulation of apoptotic process | Any process that stops, prevents, or reduces the frequency, rate or extent of cell death by apoptotic process. |
| negative regulation of canonical Wnt signaling pathway | Any process that decreases the rate, frequency, or extent of the Wnt signaling pathway through beta-catenin, the series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes. |
| negative regulation of hippo signaling | Any process that stops, prevents, or reduces the frequency, rate or extent of hippo signaling. |
| negative regulation of insulin receptor signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of insulin receptor signaling. |
| negative regulation of peptidoglycan recognition protein signaling pathway | Any process that decreases the rate, frequency, or extent of the peptidoglycan recognition protein signaling pathway. |
| negative regulation of phosphatidylinositol 3-kinase signaling | Any process that stops, prevents, or reduces the frequency, rate or extent of signal transduction mediated by the phosphatidylinositol 3-kinase cascade. |
| negative regulation of protein kinase B signaling | Any process that stops, prevents, or reduces the frequency, rate or extent of protein kinase B signaling, a series of reactions mediated by the intracellular serine/threonine kinase protein kinase B. |
| negative regulation of smoothened signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of smoothened signaling. |
| positive regulation of neuron remodeling | Any process that activates or increases the frequency, rate or extent of neuron remodeling. |
| positive regulation of proteasomal ubiquitin-dependent protein catabolic process | Any process that activates or increases the frequency, rate or extent of the breakdown of a protein or peptide by hydrolysis of its peptide bonds, initiated by the covalent attachment of ubiquitin, and mediated by the proteasome. |
| positive regulation of protein ubiquitination | Any process that activates or increases the frequency, rate or extent of the addition of ubiquitin groups to a protein. |
| positive regulation of synaptonemal complex assembly | Any process that activates or increases the frequency, rate or extent of synaptonemal complex assembly. |
| protein catabolic process | The chemical reactions and pathways resulting in the breakdown of a protein by the destruction of the native, active configuration, with or without the hydrolysis of peptide bonds. |
| protein K11-linked ubiquitination | A protein ubiquitination process in which ubiquitin monomers are attached to a protein, and then ubiquitin polymers are formed by linkages between lysine residues at position 11 of the ubiquitin monomers. K11-linked polyubiquitination targets the substrate protein for degradation. The anaphase-promoting complex promotes the degradation of mitotic regulators by assembling K11-linked polyubiquitin chains. |
| protein ubiquitination | The process in which one or more ubiquitin groups are added to a protein. |
| SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | The chemical reactions and pathways resulting in the breakdown of a protein or peptide by hydrolysis of its peptide bonds, initiated by the covalent attachment of ubiquitin, with ubiquitin-protein ligation catalyzed by an SCF (Skp1/Cul1/F-box protein) complex, and mediated by the proteasome. |
3 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q12018 | CDC53 | Cell division control protein 53 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
| Q13616 | CUL1 | Cullin-1 | Homo sapiens (Human) | PR |
| P0CH31 | At1g43140 | Putative cullin-like protein 1 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MNRSGNSQTT | QKLVNLDDIW | SELVEGIMQV | FEHEKSLTRS | QYMRFYTHVY | DYCTSVSAAP |
| 70 | 80 | 90 | 100 | 110 | 120 |
| SGRSSGKTGG | AQLVGKKLYD | RLEQFLKSYL | SELLTKFKAI | SGEEVLLSRY | TKQWKSYQFS |
| 130 | 140 | 150 | 160 | 170 | 180 |
| STVLDGICNY | LNRNWVKREC | EEGQKGIYKI | YRLALVAWKG | HLFQVLNEPV | TKAVLKSIEE |
| 190 | 200 | 210 | 220 | 230 | 240 |
| ERQGKLINRS | LVRDVIECYV | ELSFNEEDTD | AEQQKLSVYK | QNFENKFIAD | TSAFYEKESD |
| 250 | 260 | 270 | 280 | 290 | 300 |
| AFLSTNTVTE | YLKHVENRLE | EETQRVRGFN | SKNGLSYLHE | TTADVLKSTC | EEVLIEKHLK |
| 310 | 320 | 330 | 340 | 350 | 360 |
| IFHTEFQNLL | NADRNDDLKR | MYSLVALSSK | NLTDLKSILE | NHILHQGTEA | IAKCCTTDAA |
| 370 | 380 | 390 | 400 | 410 | 420 |
| NDPKTYVQTI | LDVHKKYNAL | VLTAFNNDNG | FVAALDKACG | KFINSNVVTI | ANSASKSPEL |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LAKYCDLLLK | KSSKNPEDKE | LEDNLNQVMV | VFKYIEDKDV | FQKYYSKMLA | KRLVNHTSAS |
| 490 | 500 | 510 | 520 | 530 | 540 |
| DDAEAMMISK | LKQTCGYEYT | VKLQRMFQDI | GVSKDLNSYF | KQYLAEKNLT | MEIDFGIEVL |
| 550 | 560 | 570 | 580 | 590 | 600 |
| SSGSWPFQLS | NNFLLPSELE | RSVRQFNEFY | AARHSGRKLN | WLYQMCKGEL | IMNVNRNNSS |
| 610 | 620 | 630 | 640 | 650 | 660 |
| TYTLQASTFQ | MSVLLQFNDQ | LSFTVQQLQD | NTQTQQENLI | QVLQILLKAK | VLTSSDNENS |
| 670 | 680 | 690 | 700 | 710 | 720 |
| LTPESTVELF | LDYKNKKRRI | NINQPLKTEL | KVEQETVHKH | IEEDRKLLIQ | AAIVRIMKMR |
| 730 | 740 | 750 | 760 | 770 | |
| KRLNHTNLIS | EVLNQLSTRF | KPKVPVIKKC | IDILIEKEYL | ERMEGHKDTY | SYLA |