Other names published for CHS3: CAL1, CSD2, DIT101, KTI2, chitin synthase CHS3, YBR023C
CHS3 LITERATURE TOPICS
- Curated Literature
- Genetics/Cell Biology
- Nucleic Acid Information
- Gene Product Information
- Protein Physical Properties
- Protein Processing/Modification/Regulation
- Protein Sequence Features
- Protein-protein Interactions
- Substrates/Ligands/Cofactors
- Related Genes/Proteins
- Research Aids
- Genome-wide Analysis
- Proteome-wide Analysis
- Other Topics
- Additional Information
CHS3 - Protein Processing/Modification/Regulation (22)
| Reference | Other Genes Addressed |
|---|---|
| Breidenbach MA, et al. (2012) Mapping yeast N-glycosites with isotopically recoded glycans. Mol Cell Proteomics 11(6):M111.015339 | |
| Sacristan C, et al. (2012) Neck compartmentalization as the molecular basis for the different endocytic behaviour of Chs3 during budding or hyperpolarized growth in yeast cells. Mol Microbiol 83(6):1124-35 | |
| Starr TL, et al. (2012) Sorting Signals That Mediate Traffic of Chitin Synthase III between the TGN/Endosomes and to the Plasma Membrane in Yeast. PLoS One 7(10):e46386 | |
| Martin-Garcia R, et al. (2011) The FN3 and BRCT motifs in the exomer component Chs5p define a conserved module that is necessary and sufficient for its function. Cell Mol Life Sci 68(17):2907-17 | |
| Szopinska A, et al. (2011) Rapid response of the yeast plasma membrane proteome to salt stress. Mol Cell Proteomics 10(11):M111.009589 | |
| Meissner D, et al. (2010) A Novel Role of the Yeast CaaX Protease Ste24 in Chitin Synthesis. Mol Biol Cell 21(14):2425-33 | |
| Schmidt M, et al. (2010) Boric Acid Disturbs Cell Wall Synthesis in Saccharomyces cerevisiae. Int J Microbiol 2010():930465 | |
| Ke S, et al. (2009) 1,3,4-Oxadiazoline derivatives as novel potential inhibitors targeting chitin biosynthesis: design, synthesis and biological evaluation. Bioorg Med Chem Lett 19(2):332-5 | |
| Rockwell NC, et al. (2009) ABC transporter Pdr10 regulates the membrane microenvironment of Pdr12 in Saccharomyces cerevisiae. J Membr Biol 229(1):27-52 | |
| Reyes A, et al. (2007) Chitin synthase III requires Chs4p-dependent translocation of Chs3p into the plasma membrane. J Cell Sci 120(Pt 12):1998-2009 | |
| Lam KK, et al. (2006) Palmitoylation by the DHHC protein Pfa4 regulates the ER exit of Chs3. J Cell Biol 174(1):19-25 | |
| Tahirovic S, et al. (2003) Role for lipid signaling and the cell integrity MAP kinase cascade in yeast septum biogenesis. Curr Genet 43(2):71-8 | |
| Cabib E (2000) On the zymogenic character of chitin synthase 3. Microbiology 146 ( Pt 8):1760-1 | |
| Santos B and Snyder M (2000) Sbe2p and sbe22p, two homologous Golgi proteins involved in yeast cell wall formation. Mol Biol Cell 11(2):435-52 | |
| Trilla JA, et al. (1999) Chs7p, a new protein involved in the control of protein export from the endoplasmic reticulum that is specifically engaged in the regulation of chitin synthesis in Saccharomyces cerevisiae. J Cell Biol 145(6):1153-63 | |
| Holthuis JCM, et al. (1998) The syntaxin Tlg1p mediates trafficking of chitin synthase III to polarized growth sites in yeast. Mol Biol Cell 9(12):3383-97 | |
| Ziman M, et al. (1996) Chs1p and Chs3p, two proteins involved in chitin synthesis, populate a compartment of the Saccharomyces cerevisiae endocytic pathway. Mol Biol Cell 7(12):1909-19 | |
| Choi WJ, et al. (1994) Are yeast chitin synthases regulated at the transcriptional or the posttranslational level? Mol Cell Biol 14(12):7685-94 | |
| Choi WJ, et al. (1994) Chitin synthase 3 from yeast has zymogenic properties that depend on both the CAL1 and the CAL3 genes. Proc Natl Acad Sci U S A 91(11):4727-30 | |
| Fernandez MP, et al. (1982) Activation of chitin synthetase in permeabilized cells of a Saccharomyces cerevisiae mutant lacking proteinase B. J Bacteriol 152(3):1255-64 | |
| Duran A and Cabib E (1978) Solubilization and partial purification of yeast chitin synthetase. Confirmation of the zymogenic nature of the enzyme. J Biol Chem 253(12):4419-25 | |
| Cabib E, et al. (1973) Yeast chitin synthetase. Separation of the zymogen from its activating factor and recovery of the latter in the vacuole fraction. J Biol Chem 248(4):1451-8 |



