Other names published for CDC33: TIF45, eIF4E, YOL139C
CDC33 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
CDC33 - Primary Literature (68)
| Reference | Other Genes Addressed |
|---|---|
| Firczuk H, et al. (2013) An in vivo control map for the eukaryotic mRNA translation machinery. Mol Syst Biol 9():635 | |
| Blewett NH and Goldstrohm AC (2012) A eukaryotic translation initiation factor 4E-binding protein promotes mRNA decapping and is required for PUF repression. Mol Cell Biol 32(20):4181-94 | |
| Ross D, et al. (2012) eIF4E Is an Important Determinant of Adhesion and Pseudohyphal Growth of the Yeast S. cerevisiae. PLoS One 7(11):e50773 | |
| Tkach JM, et al. (2012) Dissecting DNA damage response pathways by analysing protein localization and abundance changes during DNA replication stress. Nat Cell Biol 14(9):966-76 | |
| Tudisca V, et al. (2012) PKA isoforms coordinate mRNA fate during nutrient starvation. J Cell Sci 125(Pt 21):5221-32 | |
| Wang X, et al. (2012) Use of the novel technique of analytical ultracentrifugation with fluorescence detection system identifies a 77S monosomal translation complex. Protein Sci 21(9):1253-68 | |
| Buchan JR, et al. (2011) Stress-specific composition, assembly and kinetics of stress granules in Saccharomyces cerevisiae. J Cell Sci 124(Pt 2):228-39 | |
| Castelli LM, et al. (2011) Glucose depletion inhibits translation initiation via eIF4A loss and subsequent 48S preinitiation complex accumulation, while the pentose phosphate pathway is coordinately up-regulated. Mol Biol Cell 22(18):3379-93 | |
| Grunau S, et al. (2011) The phosphoinositide 3-kinase Vps34p is required for pexophagy in Saccharomyces cerevisiae. Biochem J 434(1):161-170 | |
| Kiraga-Motoszko K, et al. (2011) Thermodynamics of molecular recognition of mRNA 5' cap by yeast eukaryotic initiation factor 4E. J Phys Chem B 115(27):8746-54 | |
| Feketova Z, et al. (2010) Ambiguous decoding of the CUG codon alters the functionality of the Candida albicans translation initiation factor 4E. FEMS Yeast Res 10(5):558-69 | |
| Watanabe R, et al. (2010) The eukaryotic initiation factor (eIF) 4G HEAT domain promotes translation re-initiation in yeast both dependent on and independent of eIF4A mRNA helicase. J Biol Chem 285(29):21922-33 | |
| Gregio AP, et al. (2009) eIF5A has a function in the elongation step of translation in yeast. Biochem Biophys Res Commun 380(4):785-90 | |
| Buchan JR, et al. (2008) P bodies promote stress granule assembly in Saccharomyces cerevisiae. J Cell Biol 183(3):441-55 | |
| Charron C, et al. (2008) Natural variation and functional analyses provide evidence for co-evolution between plant eIF4E and potyviral VPg. Plant J 54(1):56-68 | |
| German-Retana S, et al. (2008) Mutational analysis of plant cap-binding protein eIF4E reveals key amino acids involved in biochemical functions and potyvirus infection. J Virol 82(15):7601-12 | |
| Brengues M and Parker R (2007) Accumulation of polyadenylated mRNA, Pab1p, eIF4E, and eIF4G with P-bodies in Saccharomyces cerevisiae. Mol Biol Cell 18(7):2592-602 | |
| Hoyle NP, et al. (2007) Stress-dependent relocalization of translationally primed mRNPs to cytoplasmic granules that are kinetically and spatially distinct from P-bodies. J Cell Biol 179(1):65-74 | |
| Sangthong P, et al. (2007) Distributed control for recruitment, scanning and subunit joining steps of translation initiation. Nucleic Acids Res 35(11):3573-80 | |
| Fernandez-Murray JP and McMaster CR (2006) Identification of novel phospholipid binding proteins in Saccharomyces cerevisiae. FEBS Lett 580(1):82-6 | |
| Gao Q, et al. (2005) Cap-binding protein 1-mediated and eukaryotic translation initiation factor 4E-mediated pioneer rounds of translation in yeast. Proc Natl Acad Sci U S A 102(12):4258-63 | |
| Hernandez G, et al. (2005) Functional analysis of seven genes encoding eight translation initiation factor 4E (eIF4E) isoforms in Drosophila. Mech Dev 122(4):529-43 | |
| Komar AA, et al. (2005) Novel characteristics of the biological properties of the yeast Saccharomyces cerevisiae eukaryotic initiation factor 2A. J Biol Chem 280(16):15601-11 | |
| Li L and Wang CC (2005) Identification in the ancient protist Giardia lamblia of two eukaryotic translation initiation factor 4E homologues with distinctive functions. Eukaryot Cell 4(5):948-59 | |
| Robalino J, et al. (2004) Two zebrafish eIF4E family members are differentially expressed and functionally divergent. J Biol Chem 279(11):10532-41 | |
| Gross JD, et al. (2003) Ribosome loading onto the mRNA cap is driven by conformational coupling between eIF4G and eIF4E. Cell 115(6):739-50 | |
| He H, et al. (2003) The yeast eukaryotic initiation factor 4G (eIF4G) HEAT domain interacts with eIF1 and eIF5 and is involved in stringent AUG selection. Mol Cell Biol 23(15):5431-45 | |
| Ramirez CV, et al. (2002) Modulation of eukaryotic mRNA stability via the cap-binding translation complex eIF4F. J Mol Biol 318(4):951-62 | |
| von der Haar T and McCarthy JE (2002) Intracellular translation initiation factor levels in Saccharomyces cerevisiae and their role in cap-complex function. Mol Microbiol 46(2):531-44 | |
| Anthony C, et al. (2001) Overexpression of eIF4E in Saccharomyces cerevisiae causes slow growth and decreased alpha-factor response through alterations in CLN3 expression. J Biol Chem 276(43):39645-52 |




