Two different classes of E2 ubiquitin-conjugating enzymes are required for the mono-ubiquitination of proteins and elongation by polyubiquitin chains with a specific topology
about
ZNRF2 is released from membranes by growth factors and, together with ZNRF1, regulates the Na+/K+ATPaseRegulation of androgen receptor transcriptional activity and specificity by RNF6-induced ubiquitinationAtypical ubiquitin chains: new molecular signals. 'Protein Modifications: Beyond the Usual Suspects' review seriesE2 enzymes: more than just middle menInteractions between the quality control ubiquitin ligase CHIP and ubiquitin conjugating enzymesA bacterial genetic selection system for ubiquitylation cascade discoveryMechanism and disease association of E2-conjugating enzymes: lessons from UBE2T and UBE2L3A Decade of Boon or Burden: What Has the CHIP Ever Done for Cellular Protein Quality Control Mechanism Implicated in Neurodegeneration and Aging?E2s: structurally economical and functionally repleteBuilding ubiquitin chains: E2 enzymes at workSymmetry breaking during homodimeric assembly activates an E3 ubiquitin ligaseYOD1/TRAF6 association balances p62-dependent IL-1 signaling to NF-κBMonoubiquitination promotes calpain cleavage of the protein phosphatase 2A (PP2A) regulatory subunit α4, altering PP2A stability and microtubule-associated protein phosphorylation.The ubiquitin-interacting motif protein, S5a, is ubiquitinated by all types of ubiquitin ligases by a mechanism different from typical substrate recognitionUBE2S drives elongation of K11-linked ubiquitin chains by the anaphase-promoting complexUbe2j2 ubiquitinates hydroxylated amino acids on ER-associated degradation substrates.Roles of the TRAF6 and Pellino E3 ligases in MyD88 and RANKL signaling.Copper: from neurotransmission to neuroproteostasisThe laforin-malin complex, involved in Lafora disease, promotes the incorporation of K63-linked ubiquitin chains into AMP-activated protein kinase beta subunits.The E3 ligase CHIP mediates ubiquitination and degradation of mixed-lineage kinase 3TR-FRET-based high-throughput screening assay for identification of UBC13 inhibitors.Loop 7 of E2 enzymes: an ancestral conserved functional motif involved in the E2-mediated steps of the ubiquitination cascade.Emerging complexity of protein ubiquitination in the NF-κB pathway.NF-κB/Rel proteins and the humoral immune responses of Drosophila melanogaster.E2 conjugating enzyme selectivity and requirements for function of the E3 ubiquitin ligase CHIP.Residues 240-250 in the C-terminus of the Pirh2 protein complement the function of the RING domain in self-ubiquitination of the Pirh2 protein.The anti-inflammatory drug BAY 11-7082 suppresses the MyD88-dependent signalling network by targeting the ubiquitin system.Identification of the phosphorylation sites on the E3 ubiquitin ligase Pellino that are critical for activation by IRAK1 and IRAK4.Novel inhibitors of Rad6 ubiquitin conjugating enzyme: design, synthesis, identification, and functional characterization.The multiple layers of ubiquitin-dependent cell cycle control.The role of the ubiquitin proteasome system in ischemia and ischemic tolerance.Activation of duck RIG-I by TRIM25 is independent of anchored ubiquitin.Spatiotemporal regulation of posttranslational modifications in the DNA damage response.Specificity and disease in the ubiquitin systemUpregulated expression of ubiquitin-conjugating enzyme E2Q1 (UBE2Q1) is associated with enhanced cell proliferation and poor prognosis in human hapatocellular carcinoma.Ubc13 and COOH terminus of Hsp70-interacting protein (CHIP) are required for growth hormone receptor endocytosis.Innate immune signaling in Drosophila is regulated by transforming growth factor β (TGFβ)-activated kinase (Tak1)-triggered ubiquitin editing.Chaperone-directed ubiquitylation maintains proteostasis at the expense of longevity.Histone H1 couples initiation and amplification of ubiquitin signalling after DNA damage.Oligomerization-primed coiled-coil domain interaction with Ubc13 confers processivity to TRAF6 ubiquitin ligase activity
P2860
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P2860
Two different classes of E2 ubiquitin-conjugating enzymes are required for the mono-ubiquitination of proteins and elongation by polyubiquitin chains with a specific topology
description
2008 nî lūn-bûn
@nan
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Two different classes of E2 ub ...... hains with a specific topology
@ast
Two different classes of E2 ub ...... hains with a specific topology
@en
Two different classes of E2 ub ...... hains with a specific topology
@en-gb
Two different classes of E2 ub ...... hains with a specific topology
@nl
type
label
Two different classes of E2 ub ...... hains with a specific topology
@ast
Two different classes of E2 ub ...... hains with a specific topology
@en
Two different classes of E2 ub ...... hains with a specific topology
@en-gb
Two different classes of E2 ub ...... hains with a specific topology
@nl
prefLabel
Two different classes of E2 ub ...... hains with a specific topology
@ast
Two different classes of E2 ub ...... hains with a specific topology
@en
Two different classes of E2 ub ...... hains with a specific topology
@en-gb
Two different classes of E2 ub ...... hains with a specific topology
@nl
P2093
P921
P3181
P356
P1433
P1476
Two different classes of E2 ub ...... hains with a specific topology
@en
P2093
Mark Peggie
Mark Windheim
Philip Cohen
P3181
P356
10.1042/BJ20071338
P407
P577
2008-02-01T00:00:00Z