Other names published for HUL5: ubiquitin-ubiquitin ligase HUL5, YGL141W
HUL5 LITERATURE TOPICS
- Curated Literature
- Additional Literature
- All Curated References
- Primary Literature
- Reviews
- Genetics/Cell Biology
- Nucleic Acid Information
- Gene Product Information
- Related Genes/Proteins
- Research Aids
- Genome-wide Analysis
- Proteome-wide Analysis
- Other Topics
- Additional Information
HUL5 - Additional Literature (19)
| Reference | Other Genes Addressed |
|---|---|
| Peth A, et al. (2013) Ubiquitinated proteins activate the proteasomal ATPases by binding to Usp14 or Uch37 homologs. J Biol Chem 288(11):7781-90 | |
| Ha SW, et al. (2012) The N-terminal domain of Rpn4 serves as a portable ubiquitin-independent degron and is recognized by specific 19S RP subunits. Biochem Biophys Res Commun 419(2):226-31 | |
| Kimura A, et al. (2012) N-myristoylation of the Rpt2 subunit regulates intracellular localization of the yeast 26S proteasome. Biochemistry 51(44):8856-66 | |
| Takagi K, et al. (2012) Structural basis for specific recognition of Rpt1p, an ATPase subunit of 26 S proteasome, by proteasome-dedicated chaperone Hsm3p. J Biol Chem 287(15):12172-82 | |
| Henderson A, et al. (2011) Dependence of proteasome processing rate on substrate unfolding. J Biol Chem 286(20):17495-502 | |
| Chandra A, et al. (2010) Synthetic lethality of rpn11-1 rpn10Delta is linked to altered proteasome assembly and activity. Curr Genet 56(6):543-57 | |
| Isasa M, et al. (2010) Monoubiquitination of RPN10 regulates substrate recruitment to the proteasome. Mol Cell 38(5):733-45 | |
| Bech-Otschir D, et al. (2009) Polyubiquitin substrates allosterically activate their own degradation by the 26S proteasome. Nat Struct Mol Biol 16(2):219-25 | |
| Chen AK, et al. (2009) Response of Saccharomyces cerevisiae to stress-free acidification. J Microbiol 47(1):1-8 | |
| Prakash S, et al. (2009) Substrate selection by the proteasome during degradation of protein complexes. Nat Chem Biol 5(1):29-36 | |
| Schafer A and Wolf DH (2009) Sec61p is part of the endoplasmic reticulum-associated degradation machinery. EMBO J 28(19):2874-84 | |
| Li F, et al. (2008) Thiopurine S-methyltransferase pharmacogenetics: autophagy as a mechanism for variant allozyme degradation. Pharmacogenet Genomics 18(12):1083-94 | |
| Liu C, et al. (2007) Proteasome inhibition in wild-type yeast Saccharomyces cerevisiae cells. Biotechniques 42(2):158, 160, 162 | |
| Smith DM, et al. (2007) Docking of the proteasomal ATPases' carboxyl termini in the 20S proteasome's alpha ring opens the gate for substrate entry. Mol Cell 27(5):731-44 | |
| Denison C and Kodadek T (2004) Toward a general chemical method for rapidly mapping multi-protein complexes. J Proteome Res 3(3):417-25 | |
| Schade B, et al. (2004) Cold adaptation in budding yeast. Mol Biol Cell 15(12):5492-502 | |
| Takahashi K, et al. (2004) Cellular signaling mediated by calphoglin-induced activation of IPP and PGM. Biochem Biophys Res Commun 325(1):203-14 | |
| Huh WK, et al. (2003) Global analysis of protein localization in budding yeast. Nature 425(6959):686-91 | |
| Loidl G, et al. (1999) Bivalency as a principle for proteasome inhibition. Proc Natl Acad Sci U S A 96(10):5418-22 |





