scholarly article | Q13442814 |
P356 | DOI | 10.1074/MCP.R112.021154 |
P8608 | Fatcat ID | release_vmnjojt7zvegxos2q4sbol22fe |
P932 | PMC publication ID | 3518111 |
P698 | PubMed publication ID | 22962057 |
P50 | author | Jeffrey W. Harper | Q57326226 |
P2093 | author name string | Meng-Kwang Marcus Tan | |
P2860 | cites work | SCFbetaTrCP-mediated degradation of Claspin regulates recovery from the DNA replication checkpoint response | Q24298620 |
An OBSL1-Cul7Fbxw8 Ubiquitin Ligase Signaling Mechanism Regulates Golgi Morphology and Dendrite Patterning | Q24302459 | ||
SCFFbxl3 controls the oscillation of the circadian clock by directing the degradation of cryptochrome proteins | Q24304073 | ||
Prophase destruction of Emi1 by the SCF(betaTrCP/Slimb) ubiquitin ligase activates the anaphase promoting complex to allow progression beyond prometaphase | Q24304123 | ||
Ubiquitin-dependent regulation of COPII coat size and function | Q24305964 | ||
Structure of a beta-TrCP1-Skp1-beta-catenin complex: destruction motif binding and lysine specificity of the SCF(beta-TrCP1) ubiquitin ligase | Q24306203 | ||
Structural insights into NEDD8 activation of cullin-RING ligases: conformational control of conjugation | Q24314520 | ||
Defining the human deubiquitinating enzyme interaction landscape | Q24315885 | ||
Control of iron homeostasis by an iron-regulated ubiquitin ligase | Q24317234 | ||
An E3 ligase possessing an iron-responsive hemerythrin domain is a regulator of iron homeostasis | Q24317309 | ||
Cyclin F-mediated degradation of ribonucleotide reductase M2 controls genome integrity and DNA repair | Q24336569 | ||
SCF(Cyclin F) controls centrosome homeostasis and mitotic fidelity through CP110 degradation | Q24337147 | ||
Systematic analysis and nomenclature of mammalian F-box proteins | Q24561715 | ||
The SCFbeta-TRCP-ubiquitin ligase complex associates specifically with phosphorylated destruction motifs in IkappaBalpha and beta-catenin and stimulates IkappaBalpha ubiquitination in vitro | Q24608829 | ||
Systematic and quantitative assessment of the ubiquitin-modified proteome | Q24634631 | ||
Deregulated proteolysis by the F-box proteins SKP2 and beta-TrCP: tipping the scales of cancer | Q24648025 | ||
SCFbeta-TRCP controls oncogenic transformation and neural differentiation through REST degradation | Q24653723 | ||
RINGs of good and evil: RING finger ubiquitin ligases at the crossroads of tumour suppression and oncogenesis | Q26853207 | ||
Structure of a Fbw7-Skp1-cyclin E complex: multisite-phosphorylated substrate recognition by SCF ubiquitin ligases | Q27644446 | ||
RING domain E3 ubiquitin ligases | Q27860546 | ||
The ubiquitin system | Q27860803 | ||
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 | ||
SCF ubiquitin protein ligases and phosphorylation-dependent proteolysis | Q27937519 | ||
Comprehensive identification of substrates for F-box proteins by differential proteomics analysis | Q83959951 | ||
Use of Proteome Arrays to Globally Identify Substrates for E3 Ubiquitin Ligases | Q84815219 | ||
A Complex of Cdc4p, Skp1p, and Cdc53p/Cullin Catalyzes Ubiquitination of the Phosphorylated CDK Inhibitor Sic1p | Q27939049 | ||
Function and regulation of cullin-RING ubiquitin ligases | Q28131707 | ||
Multisite phosphorylation of a CDK inhibitor sets a threshold for the onset of DNA replication | Q28209282 | ||
A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles | Q28247080 | ||
mTOR drives its own activation via SCF(βTrCP)-dependent degradation of the mTOR inhibitor DEPTOR | Q28251026 | ||
mTOR generates an auto-amplification loop by triggering the βTrCP- and CK1α-dependent degradation of DEPTOR | Q28251047 | ||
Destruction of Claspin by SCFbetaTrCP restrains Chk1 activation and facilitates recovery from genotoxic stress | Q28255529 | ||
S6K1- and betaTRCP-mediated degradation of PDCD4 promotes protein translation and cell growth | Q28269583 | ||
Control of chromosome stability by the beta-TrCP-REST-Mad2 axis | Q28273354 | ||
The SCF ubiquitin ligase: insights into a molecular machine | Q28279993 | ||
Comparison of substrate specificity of the ubiquitin ligases Nedd4 and Nedd4-2 using proteome arrays | Q28566104 | ||
Regulation of postsynaptic RapGAP SPAR by Polo-like kinase 2 and the SCFbeta-TRCP ubiquitin ligase in hippocampal neurons | Q28577634 | ||
A proteomics approach to understanding protein ubiquitination | Q29547312 | ||
FBW7 ubiquitin ligase: a tumour suppressor at the crossroads of cell division, growth and differentiation | Q29616127 | ||
An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer | Q29616732 | ||
Physiological functions of the HECT family of ubiquitin ligases | Q29617293 | ||
Whose end is destruction: cell division and the anaphase-promoting complex | Q29618257 | ||
Building ubiquitin chains: E2 enzymes at work | Q29619578 | ||
How the cyclin became a cyclin: regulated proteolysis in the cell cycle | Q33641413 | ||
The anaphase-promoting complex: it's not just for mitosis any more. | Q34147374 | ||
Global analysis of lysine ubiquitination by ubiquitin remnant immunoaffinity profiling | Q34159143 | ||
Constructing and decoding unconventional ubiquitin chains. | Q34182233 | ||
Identification of mutations in CUL7 in 3-M syndrome | Q34448386 | ||
The Fbw7 tumor suppressor regulates glycogen synthase kinase 3 phosphorylation-dependent c-Myc protein degradation | Q34835596 | ||
Identification of SCF ubiquitin ligase substrates by global protein stability profiling | Q34874145 | ||
SCF ubiquitin ligases in the maintenance of genome stability | Q35754115 | ||
PINK1- and Parkin-mediated mitophagy at a glance | Q36851332 | ||
Multimodal activation of the ubiquitin ligase SCF by Nedd8 conjugation | Q37101488 | ||
The multiple layers of ubiquitin-dependent cell cycle control. | Q37369189 | ||
Degradation of ubiquitin: the fate of the cellular reaper | Q37682565 | ||
The cullin protein family | Q37873586 | ||
SCF(FBXO22) regulates histone H3 lysine 9 and 36 methylation levels by targeting histone demethylase KDM4A for ubiquitin-mediated proteasomal degradation. | Q38285971 | ||
Quantitative proteomic analysis of cellular protein modulation upon inhibition of the NEDD8-activating enzyme by MLN4924. | Q39451819 | ||
Global identification of modular cullin-RING ligase substrates | Q39462405 | ||
Changes in the ratio of free NEDD8 to ubiquitin triggers NEDDylation by ubiquitin enzymes | Q41141041 | ||
The cyclin box fold: protein recognition in cell-cycle and transcription control | Q41684087 | ||
The v-Jun point mutation allows c-Jun to escape GSK3-dependent recognition and destruction by the Fbw7 ubiquitin ligase | Q46603785 | ||
P433 | issue | 12 | |
P304 | page(s) | 1541-1550 | |
P577 | publication date | 2012-09-07 | |
P1433 | published in | Molecular & Cellular Proteomics | Q6895932 |
P1476 | title | Understanding cullin-RING E3 biology through proteomics-based substrate identification | |
P478 | volume | 11 |
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Q38681448 | Parallel SCF adaptor capture proteomics reveals a role for SCFFBXL17 in NRF2 activation via BACH1 repressor turnover. |
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Q36666402 | Refined preparation and use of anti-diglycine remnant (K-ε-GG) antibody enables routine quantification of 10,000s of ubiquitination sites in single proteomics experiments. |
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