Other names published for SEC72: SEC67, SIM2, YLR292C
SEC72 LITERATURE TOPICS
- Curated Literature
- Genetics/Cell Biology
- Cellular Location
- Function/Process
- Genetic Interactions
- Mutants/Phenotypes
- Nucleic Acid Information
- Gene Product Information
- Related Genes/Proteins
- Research Aids
- Genome-wide Analysis
- Other Topics
- Additional Information
SEC72 - Mutants/Phenotypes (10)
| Reference | Other Genes Addressed |
|---|---|
| Wu MJ, et al. (2012) Delineation of the molecular mechanism for disulfide stress-induced aluminium toxicity. Biometals 25(3):553-61 | |
| Arias P, et al. (2011) Genome-wide survey of yeast mutations leading to activation of the yeast cell integrity MAPK pathway: Novel insights into diverse MAPK outcomes. BMC Genomics 12(1):390 | |
| Villa-Garcia MJ, et al. (2011) Genome-wide screen for inositol auxotrophy in Saccharomyces cerevisiae implicates lipid metabolism in stress response signaling. Mol Genet Genomics 285(2):125-49 | |
| Breinig F, et al. (2006) Dissecting toxin immunity in virus-infected killer yeast uncovers an intrinsic strategy of self-protection. Proc Natl Acad Sci U S A 103(10):3810-5 | |
| Brizzio V, et al. (1999) Genetic interactions between KAR7/SEC71, KAR8/JEM1, KAR5, and KAR2 during nuclear fusion in Saccharomyces cerevisiae. Mol Biol Cell 10(3):609-26 | |
| Ng DT and Walter P (1996) ER membrane protein complex required for nuclear fusion. J Cell Biol 132(4):499-509 | |
| Dahmann C, et al. (1995) S-phase-promoting cyclin-dependent kinases prevent re-replication by inhibiting the transition of replication origins to a pre-replicative state. Curr Biol 5(11):1257-69 | |
| Feldheim D and Schekman R (1994) Sec72p contributes to the selective recognition of signal peptides by the secretory polypeptide translocation complex. J Cell Biol 126(4):935-43 | |
| Brodsky JL and Schekman R (1993) A Sec63p-BiP complex from yeast is required for protein translocation in a reconstituted proteoliposome. J Cell Biol 123(6 Pt 1):1355-63 | |
| Green N, et al. (1992) Mutants in three novel complementation groups inhibit membrane protein insertion into and soluble protein translocation across the endoplasmic reticulum membrane of Saccharomyces cerevisiae. J Cell Biol 116(3):597-604 |



