Pages that link to "Q40999094"
Jump to navigation
Jump to search
The following pages link to Structural requirements for O-glycosylation of the mouse hepatitis virus membrane protein (Q40999094):
Displaying 26 items.
- Assembly of the coronavirus envelope: homotypic interactions between the M proteins (Q27469592) (← links)
- Localization and Membrane Topology of Coronavirus Nonstructural Protein 4: Involvement of the Early Secretory Pathway in Replication (Q27485022) (← links)
- Topology and Membrane Anchoring of the Coronavirus Replication Complex: Not All Hydrophobic Domains of nsp3 and nsp6 Are Membrane Spanning (Q27487407) (← links)
- Functional conservation of subfamilies of putative UDP-N-acetylgalactosamine:polypeptide N-acetylgalactosaminyltransferases in Drosophila, Caenorhabditis elegans, and mammals. One subfamily composed of l(2)35Aa is essential in Drosophila (Q31046911) (← links)
- Retargeting of coronavirus by substitution of the spike glycoprotein ectodomain: crossing the host cell species barrier (Q33793489) (← links)
- Characterization of the coronavirus mouse hepatitis virus strain A59 small membrane protein E. (Q33798977) (← links)
- The carbohydrate-binding plant lectins and the non-peptidic antibiotic pradimicin A target the glycans of the coronavirus envelope glycoproteins (Q34005790) (← links)
- A conserved domain in the coronavirus membrane protein tail is important for virus assembly (Q34190645) (← links)
- Incorporation of spike and membrane glycoproteins into coronavirus virions (Q35544383) (← links)
- Site-specific analysis of von Willebrand factor O-glycosylation (Q35897602) (← links)
- The chemistry and biology of mucin-type O-linked glycosylation (Q36187831) (← links)
- The molecular biology of coronaviruses (Q36550910) (← links)
- Synthetic genes for glycoprotein design and the elucidation of hydroxyproline-O-glycosylation codes (Q36774136) (← links)
- Mapping of the coronavirus membrane protein domains involved in interaction with the spike protein (Q39550949) (← links)
- Assembly of spikes into coronavirus particles is mediated by the carboxy-terminal domain of the spike protein (Q39588413) (← links)
- Co-expressing GP5 and M proteins under different promoters in recombinant modified vaccinia virus ankara (rMVA)-based vaccine vector enhanced the humoral and cellular immune responses of porcine reproductive and respiratory syndrome virus (PRRSV). (Q40166458) (← links)
- Membrane topology of coronavirus E protein (Q40817671) (← links)
- Glycosylation of the severe acute respiratory syndrome coronavirus triple-spanning membrane proteins 3a and M. (Q41861879) (← links)
- The glycosylation status of the murine hepatitis coronavirus M protein affects the interferogenic capacity of the virus in vitro and its ability to replicate in the liver but not the brain (Q44550238) (← links)
- Thermal aggregation of SARS-CoV membrane protein (Q46603992) (← links)
- Characterization of severe acute respiratory syndrome coronavirus membrane protein (Q46915549) (← links)
- Unique N-linked glycosylation of murine coronavirus MHV-2 membrane protein at the conserved O-linked glycosylation site (Q47875847) (← links)
- Expression and membrane integration of SARS-CoV M protein (Q81045083) (← links)
- Molecular interactions in the assembly of coronaviruses (Q81155962) (← links)
- Membrane binding proteins of coronaviruses (Q84315456) (← links)
- Post-translational modifications of coronavirus proteins: roles and function (Q90576842) (← links)