145 related articles for article (PubMed ID: 33798411)
1. K29/K48-branched ubiquitin chains TRIP the alarm fueling neo-substrate degradation via the CRL2
Magtoto CM; Feltham R
Mol Cell; 2021 Apr; 81(7):1363-1365. PubMed ID: 33798411
[TBL] [Abstract][Full Text] [Related]
2. TRIP12 promotes small-molecule-induced degradation through K29/K48-branched ubiquitin chains.
Kaiho-Soma A; Akizuki Y; Igarashi K; Endo A; Shoda T; Kawase Y; Demizu Y; Naito M; Saeki Y; Tanaka K; Ohtake F
Mol Cell; 2021 Apr; 81(7):1411-1424.e7. PubMed ID: 33567268
[TBL] [Abstract][Full Text] [Related]
3. The deubiquitinase TRABID stabilizes the K29/K48-specific E3 ubiquitin ligase HECTD1.
Harris LD; Le Pen J; Scholz N; Mieszczanek J; Vaughan N; Davis S; Berridge G; Kessler BM; Bienz M; Licchesi JDF
J Biol Chem; 2021; 296():100246. PubMed ID: 33853758
[TBL] [Abstract][Full Text] [Related]
4. cIAP1-based degraders induce degradation via branched ubiquitin architectures.
Akizuki Y; Morita M; Mori Y; Kaiho-Soma A; Dixit S; Endo A; Shimogawa M; Hayashi G; Naito M; Okamoto A; Tanaka K; Saeki Y; Ohtake F
Nat Chem Biol; 2023 Mar; 19(3):311-322. PubMed ID: 36316570
[TBL] [Abstract][Full Text] [Related]
5. The HECT domain of TRIP12 ubiquitinates substrates of the ubiquitin fusion degradation pathway.
Park Y; Yoon SK; Yoon JB
J Biol Chem; 2009 Jan; 284(3):1540-9. PubMed ID: 19028681
[TBL] [Abstract][Full Text] [Related]
6. The K48-K63 Branched Ubiquitin Chain Regulates NF-κB Signaling.
Ohtake F; Saeki Y; Ishido S; Kanno J; Tanaka K
Mol Cell; 2016 Oct; 64(2):251-266. PubMed ID: 27746020
[TBL] [Abstract][Full Text] [Related]
7. K29-selective ubiquitin binding domain reveals structural basis of specificity and heterotypic nature of k29 polyubiquitin.
Kristariyanto YA; Abdul Rehman SA; Campbell DG; Morrice NA; Johnson C; Toth R; Kulathu Y
Mol Cell; 2015 Apr; 58(1):83-94. PubMed ID: 25752573
[TBL] [Abstract][Full Text] [Related]
8. Assembly and specific recognition of k29- and k33-linked polyubiquitin.
Michel MA; Elliott PR; Swatek KN; Simicek M; Pruneda JN; Wagstaff JL; Freund SM; Komander D
Mol Cell; 2015 Apr; 58(1):95-109. PubMed ID: 25752577
[TBL] [Abstract][Full Text] [Related]
9. K63 ubiquitylation triggers proteasomal degradation by seeding branched ubiquitin chains.
Ohtake F; Tsuchiya H; Saeki Y; Tanaka K
Proc Natl Acad Sci U S A; 2018 Feb; 115(7):E1401-E1408. PubMed ID: 29378950
[TBL] [Abstract][Full Text] [Related]
10. Ufd2p synthesizes branched ubiquitin chains to promote the degradation of substrates modified with atypical chains.
Liu C; Liu W; Ye Y; Li W
Nat Commun; 2017 Feb; 8():14274. PubMed ID: 28165462
[TBL] [Abstract][Full Text] [Related]
11. The parallel reaction monitoring method contributes to a highly sensitive polyubiquitin chain quantification.
Tsuchiya H; Tanaka K; Saeki Y
Biochem Biophys Res Commun; 2013 Jun; 436(2):223-9. PubMed ID: 23726910
[TBL] [Abstract][Full Text] [Related]
12. Nonproteolytic K29-Linked Ubiquitination of the PB2 Replication Protein of Influenza A Viruses by Proviral Cullin 4-Based E3 Ligases.
Karim M; Biquand E; Declercq M; Jacob Y; van der Werf S; Demeret C
mBio; 2020 Apr; 11(2):. PubMed ID: 32265326
[TBL] [Abstract][Full Text] [Related]
13. Mechanism of ubiquitin chain synthesis employed by a HECT domain ubiquitin ligase.
French ME; Klosowiak JL; Aslanian A; Reed SI; Yates JR; Hunter T
J Biol Chem; 2017 Jun; 292(25):10398-10413. PubMed ID: 28461335
[No Abstract] [Full Text] [Related]
14. HECT-Type E3 Ubiquitin Ligases in Cancer.
Bernassola F; Chillemi G; Melino G
Trends Biochem Sci; 2019 Dec; 44(12):1057-1075. PubMed ID: 31610939
[TBL] [Abstract][Full Text] [Related]
15. Ubiquitin binding by a CUE domain regulates ubiquitin chain formation by ERAD E3 ligases.
Bagola K; von Delbrück M; Dittmar G; Scheffner M; Ziv I; Glickman MH; Ciechanover A; Sommer T
Mol Cell; 2013 May; 50(4):528-39. PubMed ID: 23665229
[TBL] [Abstract][Full Text] [Related]
16. Ubiquitin chain specificities of E6AP E3 ligase and its HECT domain.
Kobayashi F; Nishiuchi T; Takaki K; Konno H
Biochem Biophys Res Commun; 2018 Feb; 496(2):686-692. PubMed ID: 29288669
[TBL] [Abstract][Full Text] [Related]
17. β-Sheet Augmentation Is a Conserved Mechanism of Priming HECT E3 Ligases for Ubiquitin Ligation.
Jäckl M; Stollmaier C; Strohäker T; Hyz K; Maspero E; Polo S; Wiesner S
J Mol Biol; 2018 Sep; 430(18 Pt B):3218-3233. PubMed ID: 29964046
[TBL] [Abstract][Full Text] [Related]
18. VPS34 K29/K48 branched ubiquitination governed by UBE3C and TRABID regulates autophagy, proteostasis and liver metabolism.
Chen YH; Huang TY; Lin YT; Lin SY; Li WH; Hsiao HJ; Yan RL; Tang HW; Shen ZQ; Chen GC; Wu KP; Tsai TF; Chen RH
Nat Commun; 2021 Feb; 12(1):1322. PubMed ID: 33637724
[TBL] [Abstract][Full Text] [Related]
19. K48- and K63-linked ubiquitin chain interactome reveals branch- and length-specific ubiquitin interactors.
Waltho A; Popp O; Lenz C; Pluska L; Lambert M; Dötsch V; Mertins P; Sommer T
Life Sci Alliance; 2024 Aug; 7(8):. PubMed ID: 38803224
[TBL] [Abstract][Full Text] [Related]
20. Arkadia (RING Finger Protein 111) Mediates Sumoylation-Dependent Stabilization of Nrf2 Through K48-Linked Ubiquitination.
McIntosh DJ; Walters TS; Arinze IJ; Davis J
Cell Physiol Biochem; 2018; 46(1):418-430. PubMed ID: 29597191
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
