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1 tes, the N-end rule pathway is a part of the ubiquitin system.
2 ther or not p53 is itself a substrate of the ubiquitin system.
3 of the receptor protein as substrate for the ubiquitin system.
4 ic regulation of mitochondrial import by the ubiquitin system.
5 iquitination is an integral component of the ubiquitin system.
6 ty of limiting metabolic enzymes through the ubiquitin system.
7 as an important regulatory layer within the ubiquitin system.
8 mechanisms to manipulate or subvert the host ubiquitin system.
9 ic AAA+ ATPase with diverse functions in the ubiquitin system.
10 igase substrate receptors independent of the ubiquitin system.
11 quitination, are important regulators of the ubiquitin system.
12 cificity gives fundamental insights into the ubiquitin system.
13 proteins and are hence key regulators of the ubiquitin system.
14 nserved regulation of Notch signaling by the ubiquitin system.
15 and mechanisms of substrate targeting by the ubiquitin system.
16 as a DAT interacting protein using the split ubiquitin system.
17 allows for the remarkable versatility of the ubiquitin system.
18 activities of kinases, phosphatases, and the ubiquitin system.
19 reted LLO is targeted for degradation by the ubiquitin system.
20 dent of VHL and p53 and does not require the ubiquitin system.
21 rades proteins tagged for destruction by the ubiquitin system.
22 o physically interact with Gpa1 in the split-ubiquitin system.
23 on of proteins marked for destruction by the ubiquitin system.
24 nct mechanism for substrate targeting in the ubiquitin system.
25 of proteins targeted for proteolysis by the ubiquitin system.
26 many otherwise dissimilar E3 proteins of the ubiquitin system.
27 dvance and the mechanics of targeting by the ubiquitin system.
28 ify the relevant targeting components of the ubiquitin system.
29 le pathway is one proteolytic pathway of the ubiquitin system.
30 A libraries using yeast-two-hybrid and split-ubiquitin systems.
31 actor at the crossroads between the SUMO and ubiquitin systems.
32 ning the highly characterized bradykinin and ubiquitin systems.
35 by the ubiquitin system, and discuss how the ubiquitin system affects proteins involved in pathogen o
36 using a high-resolution CRISPR screen of the ubiquitin system after IR, we systematically uncover gen
38 ight some emerging relationships between the ubiquitin system and disease, and discuss current and fu
39 lving membrane proteins, including the split ubiquitin system and fluorescence-based technologies for
42 We conclude that human cells utilize the ubiquitin system and NDP52 to activate autophagy against
43 ion of CSIT2 inhibits the possible damage to ubiquitin system and protein translation, which allows m
46 orts targeting the various components of the ubiquitin system and studying the role of DUBs in health
48 s both the high substrate specificity of the ubiquitin system and the variety of regulatory mechanism
49 studies on how seed size is affected by the ubiquitin system, and discuss how the ubiquitin system a
50 ide an additional layer of regulation in the ubiquitin system, and distinct conformations observed in
54 r data suggest widespread involvement of the ubiquitin system at multiple stages of the Met activatio
55 identify Cuz1/Ynl155w as a component of the ubiquitin system, capable of interacting with both the p
64 advanced our understanding of the canonical ubiquitin system, further study of noncanonical ubiquiti
65 ied multiple causal variants in each of four ubiquitin system genes whose products process (NTA1), re
70 mall molecule degraders that act through the ubiquitin system have spurred efforts to extend this tec
72 egans have identified multiple roles for the ubiquitin system in early development, where ubiquitin-d
78 ate the requirement for an active proteasome/ubiquitin system in release and maturation of infectious
79 BL1 system shares many similarities with the ubiquitin system in structures and in conjugation with e
80 findings, this study suggests a role for the ubiquitin system in the destabilization and rupture of c
82 a previous report on the involvement of the ubiquitin system in the tobacco HR [2], and validates an
83 our current understanding of the role of the ubiquitin system in various human diseases ranging from
84 ding of the disruptions to components of the ubiquitin system, in particular E3 ligases and deubiquit
85 s that are associated with components of the ubiquitin system, including ubiquitin, ubiquitin-like pr
90 ignaling pathways and how alterations in the ubiquitin system lead to the development of distinct hum
91 opment and regeneration are degraded via the ubiquitin system, little is known about the mechanisms a
96 sive neighborhoods with either a prokaryotic ubiquitin-system or a HORMA domain-PCH2-like AAA+ ATPase
98 al proteins associated with cytoskeletal and ubiquitin system proteins exhibited a more complex evolu
104 Current drug discovery activities in the ubiquitin system seek to (i) expand the development of n
107 ay in this pipeline, the drugs targeting the ubiquitin system that have been developed, and new appro
108 and MDP3/PAN1, implicate interactions of the ubiquitin system, the actin cytoskeleton and protein syn
110 er report has shown that inactivation of the ubiquitin system through blocking E1 (ubiquitin-activati
111 Thus, HD is linked to global changes in the ubiquitin system to a much greater extent than previousl
112 ffectors have evolved to manipulate the host ubiquitin system to alter host cell physiology or the lo
113 e UBA domains functionally interact with the ubiquitin system to control Pds1p degradation in respons
115 und that trametinib activates the proteasome-ubiquitin system to downregulate Id1 in KRAS-mutant LUAD
117 aspect in the manipulation of the eukaryotic ubiquitin system to facilitate bacterial replication and
119 t immune system; how plants use ethylene and ubiquitin systems to control growth and development; and
120 brane protein two-hybrid approach, the split-ubiquitin system, to address two aspects of the enzyme c
121 rated that a multifunctional molecule of the ubiquitin system ubiquitin C-terminal hydrolase L1 (UCH-
122 While ubc4Delta and other alterations of ubiquitin system used in this work cause slight inductio
123 spite the extensive efforts in targeting the ubiquitin system, very few E2 binders have currently bee
126 iquitylases (DUBs) are key regulators of the ubiquitin system which cleave ubiquitin moieties from pr
128 ective we provide a short description of the ubiquitin system, with specific emphasis given to its ro