scholarly article | Q13442814 |
P2093 | author name string | Brenda A Schulman | |
J Wade Harper | |||
Philip D Jeffrey | |||
Geng Wu | |||
Nikola P Pavletich | |||
Guozhou Xu | |||
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Structural basis for the recognition of hydroxyproline in HIF-1 alpha by pVHL | Q24299061 | ||
The SCFbeta-TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in IkappaBalpha and beta-catenin and stimulates IkappaBalpha ubiquitination in vitro | Q24608829 | ||
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The fission yeast COP9/signalosome is involved in cullin modification by ubiquitin-related Ned8p | Q24802316 | ||
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Three-dimensional structure of the armadillo repeat region of beta-catenin | Q27743283 | ||
Mechanisms underlying ubiquitination | Q27860656 | ||
The ubiquitin system | Q27860803 | ||
The human F box protein beta-Trcp associates with the Cul1/Skp1 complex and regulates the stability of beta-catenin. | Q27863647 | ||
F-Box Proteins Are Receptors that Recruit Phosphorylated Substrates to the SCF Ubiquitin-Ligase Complex | Q27934075 | ||
SKP1 connects cell cycle regulators to the ubiquitin proteolysis machinery through a novel motif, the F-box | Q27936367 | ||
A Complex of Cdc4p, Skp1p, and Cdc53p/Cullin Catalyzes Ubiquitination of the Phosphorylated CDK Inhibitor Sic1p | Q27939049 | ||
Reconstitution of G1 cyclin ubiquitination with complexes containing SCFGrr1 and Rbx1. | Q27940059 | ||
The tyrosine kinase negative regulator c-Cbl as a RING-type, E2-dependent ubiquitin-protein ligase | Q28145635 | ||
NF-kappaB regulation in the immune system | Q28205043 | ||
SUMO-1 modification of IkappaBalpha inhibits NF-kappaB activation | Q28282094 | ||
Signal-induced degradation of I kappa B alpha requires site-specific ubiquitination | Q28615601 | ||
Critical role for lysines 21 and 22 in signal-induced, ubiquitin-mediated proteolysis of I kappa B-alpha | Q28618972 | ||
β-catenin is a target for the ubiquitin–proteasome pathway | Q29547589 | ||
SCF and Cullin/Ring H2-based ubiquitin ligases | Q29547637 | ||
The oncogenic activation of beta-catenin | Q33540073 | ||
The von Hippel-Lindau tumor suppressor protein | Q34132816 | ||
Distribution of end-to-end distances of oligopeptides in solution as estimated by energy transfer | Q35078720 | ||
Regulation of E2F1 activity by acetylation | Q40387087 | ||
The F-box protein beta-TrCP associates with phosphorylated beta-catenin and regulates its activity in the cell. | Q40967633 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Beta-transducin repeat containing E3 ubiquitin protein ligase | Q21116841 |
S-phase kinase associated protein 1 | Q21149853 | ||
ubiquitin ligase activator activity | Q22313903 | ||
P304 | page(s) | 1445-56 | |
P577 | publication date | 2003-06-01 | |
P1433 | published in | Molecular Cell | Q3319468 |
P1476 | title | Structure of a beta-TrCP1-Skp1-beta-catenin complex: destruction motif binding and lysine specificity of the SCF(beta-TrCP1) ubiquitin ligase | |
P478 | volume | 11 |
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Q34025425 | Serine residues in the cytosolic tail of the T-cell antigen receptor alpha-chain mediate ubiquitination and endoplasmic reticulum-associated degradation of the unassembled protein |
Q37250049 | Setting the pace of the Neurospora circadian clock by multiple independent FRQ phosphorylation events |
Q26863643 | Short linear motifs - ex nihilo evolution of protein regulation |
Q53491312 | Signal transduction via unstructured protein conduits |
Q40355223 | Site-specific monoubiquitination of IkappaB kinase IKKbeta regulates its phosphorylation and persistent activation |
Q36176561 | Site-specific ubiquitination exposes a linear motif to promote interferon-alpha receptor endocytosis |
Q34341635 | Slmb antagonises the aPKC/Par-6 complex to control oocyte and epithelial polarity |
Q24297098 | Smad3 prevents beta-catenin degradation and facilitates beta-catenin nuclear translocation in chondrocytes |
Q92376522 | Snail1: A Transcriptional Factor Controlled at Multiple Levels |
Q38346254 | Stability of homologue of Slimb F-box protein is regulated by availability of its substrate |
Q41039086 | Stability of the PHF10 subunit of PBAF signature module is regulated by phosphorylation: role of β-TrCP. |
Q37583516 | Stable ubiquitination of human T-cell leukemia virus type 1 tax is required for proteasome binding |
Q27675990 | Structural Basis for Cul3 Protein Assembly with the BTB-Kelch Family of E3 Ubiquitin Ligases |
Q36869465 | Structural Basis for Substrate Selectivity of the E3 Ligase COP1 |
Q33552279 | Structural and functional analysis of essential pre-mRNA splicing factor Prp19p |
Q36172880 | Structural and functional characterization of Nrf2 degradation by the glycogen synthase kinase 3/β-TrCP axis |
Q34762436 | Structural assembly of cullin-RING ubiquitin ligase complexes |
Q24293794 | Structural basis for recruitment of Ubc12 by an E2 binding domain in NEDD8's E1 |
Q27644251 | Structural basis for the selection of glycosylated substrates by SCFFbs1 ubiquitin ligase |
Q24314963 | Structural basis for the specific recognition of methylated histone H3 lysine 4 by the WD-40 protein WDR5 |
Q24310859 | Structural basis of UV DNA-damage recognition by the DDB1-DDB2 complex |
Q24300948 | Structural basis of dimerization-dependent ubiquitination by the SCF(Fbx4) ubiquitin ligase |
Q24299395 | Structural basis of selective ubiquitination of TRF1 by SCFFbx4 |
Q38344257 | Structural basis of sugar-recognizing ubiquitin ligase |
Q24337721 | Structural basis of the Cks1-dependent recognition of p27(Kip1) by the SCF(Skp2) ubiquitin ligase |
Q64069399 | Structural basis of βTrCP1-associated GLI3 processing |
Q42694183 | Structural complexity in the KCTD family of Cullin3-dependent E3 ubiquitin ligases |
Q24314520 | Structural insights into NEDD8 activation of cullin-RING ligases: conformational control of conjugation |
Q35151712 | Structural regulation of cullin-RING ubiquitin ligase complexes |
Q27667443 | Structure and function of WD40 domain proteins |
Q58173499 | Structure and regulatory networks of WD40 protein in plants |
Q27670574 | Structure of a Glomulin-RBX1-CUL1 Complex: Inhibition of a RING E3 Ligase through Masking of Its E2-Binding Surface |
Q24299638 | Structure of a RING E3 trapped in action reveals ligation mechanism for the ubiquitin-like protein NEDD8 |
Q24313433 | Structure of the Cand1-Cul1-Roc1 complex reveals regulatory mechanisms for the assembly of the multisubunit cullin-dependent ubiquitin ligases |
Q27688887 | Structure of the FP domain of Fbxo7 reveals a novel mode of protein-protein interaction |
Q24298930 | Structure of the Keap1:Nrf2 interface provides mechanistic insight into Nrf2 signaling |
Q46463573 | Substrate recognition and ubiquitination of SCFSkp2/Cks1 ubiquitin-protein isopeptide ligase. |
Q36802367 | Suramin inhibits cullin-RING E3 ubiquitin ligases. |
Q95300946 | Surface charge of Merkel cell polyomavirus small T antigen determines cell transformation through allosteric FBW7 WD40 domain targeting |
Q34043797 | Targeting Cullin-RING E3 ubiquitin ligases for drug discovery: structure, assembly and small-molecule modulation |
Q37333805 | The Cdc42/Rac nucleotide exchange factor protein β1Pix (Pak-interacting exchange factor) modulates β-catenin transcriptional activity in colon cancer cells: evidence for direct interaction of β1PIX with β-catenin |
Q37849305 | The Cullin-RING Ubiquitin-Protein Ligases |
Q27664983 | The Effect of Asp-His-Ser/Thr-Trp Tetrad on the Thermostability of WD40-Repeat Proteins |
Q33419571 | The F-box protein beta-TrCp1/Fbw1a interacts with p300 to enhance beta-catenin transcriptional activity |
Q39167053 | The F-box protein β-TrCP promotes ubiquitination of TRF1 and regulates the ALT-associated PML bodies formation in U2OS cells |
Q27695666 | The FP domains of PI31 and Fbxo7 have the same protein fold but very different modes of protein-protein interaction |
Q24669733 | The Hedgehog-inducible ubiquitin ligase subunit WSB-1 modulates thyroid hormone activation and PTHrP secretion in the developing growth plate |
Q38344853 | The Multifunctions of WD40 Proteins in Genome Integrity and Cell Cycle Progression |
Q47236804 | The OsFBK1 E3 ligase subunit affects anther and root secondary cell wall thickenings by mediating turn-over of a cinnamoyl-CoA reductase. |
Q30413242 | The Plant Proteome Folding Project: Structure and Positive Selection in Plant Protein Families |
Q41817040 | The Prp19 U-box crystal structure suggests a common dimeric architecture for a class of oligomeric E3 ubiquitin ligases |
Q27661523 | The Prp19 WD40 Domain Contains a Conserved Protein Interaction Region Essential for Its Function |
Q92446155 | The Role of Ubiquitination in Regulating Embryonic Stem Cell Maintenance and Cancer Development |
Q54343211 | The Roles of Intrinsic Disorder in Orchestrating the Wnt-Pathway |
Q28279993 | The SCF ubiquitin ligase: insights into a molecular machine |
Q37562004 | The SCFβ-TRCP E3 ubiquitin ligase complex targets Lipin1 for ubiquitination and degradation to promote hepatic lipogenesis. |
Q36437659 | The SKP1-like gene family of Arabidopsis exhibits a high degree of differential gene expression and gene product interaction during development |
Q35804479 | The Structural Differences between a Glycoprotein Specific F-Box Protein Fbs1 and Its Homologous Protein FBG3. |
Q26748938 | The Ubiquitination of NF-κB Subunits in the Control of Transcription |
Q34021500 | The Vpu protein: new concepts in virus release and CD4 down-modulation |
Q34493925 | The WD40 repeats of FANCL are required for Fanconi anemia core complex assembly |
Q37496493 | The WD40-Repeat Protein-Containing Deubiquitinase Complex: Catalysis, Regulation, and Potential for Therapeutic Intervention |
Q38074799 | The WNT signaling pathway from ligand secretion to gene transcription: Molecular mechanisms and pharmacological targets |
Q38867422 | The WNT-less wonder: WNT-independent β-catenin signaling |
Q37681979 | The enzymes in ubiquitin-like post-translational modifications |
Q34028582 | The many blades of the β-propeller proteins: conserved but versatile |
Q26865781 | The many faces and functions of β-catenin |
Q35691542 | The many faces of beta-TrCP E3 ubiquitin ligases: reflections in the magic mirror of cancer |
Q33508245 | The mechanism of ubiquitination in the cullin-RING E3 ligase machinery: conformational control of substrate orientation |
Q39795993 | The myxoma virus m-t5 ankyrin repeat host range protein is a novel adaptor that coordinately links the cellular signaling pathways mediated by Akt and Skp1 in virus-infected cells |
Q41967221 | The nucleosome acidic patch plays a critical role in RNF168-dependent ubiquitination of histone H2A. |
Q44777782 | The origins and evolution of ubiquitination sites |
Q36802821 | The phospho-occupancy of an atypical SLIMB-binding site on PERIOD that is phosphorylated by DOUBLETIME controls the pace of the clock. |
Q30542776 | The rice RING finger E3 ligase, OsHCI1, drives nuclear export of multiple substrate proteins and its heterogeneous overexpression enhances acquired thermotolerance |
Q34749877 | The specificities of Kaposi's sarcoma-associated herpesvirus-encoded E3 ubiquitin ligases are determined by the positions of lysine or cysteine residues within the intracytoplasmic domains of their targets |
Q40133210 | The ubiquitin ligase SCF(betaTrCP) regulates the degradation of the growth hormone receptor |
Q24336640 | The ubiquitin-specific protease USP47 is a novel beta-TRCP interactor regulating cell survival |
Q37798661 | The various roles of ubiquitin in Wnt pathway regulation. |
Q28279593 | The β-catenin destruction complex |
Q37240247 | Thiazolidinediones mimic glucose starvation in facilitating Sp1 degradation through the up-regulation of beta-transducin repeat-containing protein |
Q42514932 | Transcriptional Regulation by Nrf2. |
Q34344682 | Transfer of Ho Endonuclease and Ufo1 to the Proteasome by the UbL-UbA Shuttle Protein, Ddi1, Analysed by Complex Formation In Vitro |
Q37113911 | Transforming growth factor-beta stimulates cyclin D1 expression through activation of beta-catenin signaling in chondrocytes |
Q43065281 | Tripartite degrons confer diversity and specificity on regulated protein degradation in the ubiquitin-proteasome system. |
Q35787947 | Tumor viruses and cell signaling pathways: deubiquitination versus ubiquitination |
Q34225698 | Twists and turns in ubiquitin‐like protein conjugation cascades |
Q36642707 | Two-site substrate recognition model for the Keap1-Nrf2 system: a hinge and latch mechanism |
Q52315014 | Ube2s stabilizes β-Catenin through K11-linked polyubiquitination to promote mesendoderm specification and colorectal cancer development |
Q38678006 | Ubiquitin, the centrosome, and chromosome segregation |
Q34958467 | Ubiquitin-conjugating enzyme Cdc34 and ubiquitin ligase Skp1-cullin-F-box ligase (SCF) interact through multiple conformations |
Q28274205 | Ubiquitination and degradation of the inhibitors of NF-kappaB |
Q58606339 | Ubiquitination in Scleroderma Fibrosis and Its Treatment |
Q37852608 | Ubiquitination in host immune response to human papillomavirus infection |
Q46568443 | Ubiquitination of p27Kip1 requires physical interaction with cyclin E and probable phosphate recognition by SKP2. |
Q42820389 | Ubiquitylation of the amino terminus of Myc by SCF(β-TrCP) antagonizes SCF(Fbw7)-mediated turnover |
Q36455676 | Understanding cullin-RING E3 biology through proteomics-based substrate identification |
Q38047273 | Unraveling the ubiquitin-regulated signaling networks by mass spectrometry-based proteomics. |
Q30370948 | Vaccinia virus protein A49 is an unexpected member of the B-cell Lymphoma (Bcl)-2 protein family |
Q33455505 | Vpu antagonizes BST-2-mediated restriction of HIV-1 release via beta-TrCP and endo-lysosomal trafficking |
Q44852706 | Vpu-mediated degradation of CD4 reconstituted in yeast reveals mechanistic differences to cellular ER-associated protein degradation |
Q35253276 | WDSPdb: a database for WD40-repeat proteins |
Q35838990 | Wilms Tumor Gene on X Chromosome (WTX) Inhibits Degradation of NRF2 Protein through Competitive Binding to KEAP1 Protein |
Q90028643 | Wnt Regulation: Exploring Axin-Disheveled interactions and defining mechanisms by which the SCF E3 ubiquitin ligase is recruited to the destruction complex |
Q24653563 | Wnt signaling: the good and the bad |
Q91910450 | Wnt/β-catenin signalling in ovarian cancer: Insights into its hyperactivation and function in tumorigenesis |
Q33307883 | Wrenches in the works: drug discovery targeting the SCF ubiquitin ligase and APC/C complexes |
Q39792638 | beta-TrCP-mediated ubiquitination and degradation of PHLPP1 are negatively regulated by Akt. |
Q28276987 | beta-catenin destruction complex: insights and questions from a structural perspective |
Q38767528 | lnc-β-Catm elicits EZH2-dependent β-catenin stabilization and sustains liver CSC self-renewal |
Q28251026 | mTOR drives its own activation via SCF(βTrCP)-dependent degradation of the mTOR inhibitor DEPTOR |
Q28251047 | mTOR generates an auto-amplification loop by triggering the βTrCP- and CK1α-dependent degradation of DEPTOR |
Q40362912 | p300 modulates ATF4 stability and transcriptional activity independently of its acetyltransferase domain |
Q57471387 | β-Catenin is a pH sensor with decreased stability at higher intracellular pH |
Q37132132 | β-Transducin Repeat-containing Protein 1 (β-TrCP1)-mediated Silencing Mediator of Retinoic Acid and Thyroid Hormone Receptor (SMRT) Protein Degradation Promotes Tumor Necrosis Factor α (TNFα)-induced Inflammatory Gene Expression |
Q39451480 | βTrCP Controls GH Receptor Degradation via Two Different Motifs |
Q38316122 | βTrCP interacts with the ubiquitin-dependent endocytosis motif of the GH receptor in an unconventional manner |
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