Category:Team Just Name It Something

in figure 2.(lane 8,9,11,12)). "This suggests that in the absence of E3, the spike glycoproteins do not form heterodimeric complexes at any

time after synthesis"(involved in virus assembly). Lobigs,M. et at.(1990).

in figure 2.(lane 8,9,11,12)). "This suggests that in the absence of E3, the spike glycoproteins do not form heterodimeric complexes at any

time after synthesis"(involved in virus assembly). Lobigs,M. et at.(1990).

in figure 2.(lane 8,9,11,12)). "This suggests that in the absence of E3, the spike glycoproteins do not form heterodimeric complexes at any

time after synthesis"(involved in virus assembly). Lobigs,M. et at.(1990).

Fig-1 shows how 6k makes the cell membrane more permeable by showing the location of tagged polypeptides in two different cells. One affected be the 6k protein and the other not.

In figure 8b, the anti-El" antibody gave a punctal staining pattern which probably represented the endosomal structures

Table 1 represents the results of the mutations on various clones to express MTase activity. Changes and/or deletions to conserved amino acid sequences in nsP1 resulted in lower Km for S-adenosyl methionine. Reduced methyl donor substrate concentration significantly reduced MTase activity and viral infectivity.

In Fig. 5

Mutant strains of sindbis virus with insertion sequences in the PE2 glycoprotein gene have significantly reduced binding capabilities. PE2 cleavage is necessary for E2/E3 specific spike protein with E2 specific for receptor binding.

See Fig. 3; Fig. 6; Fig. 7; Fig. 8

In addition, subcellular localization of 6K-Myc was analyzed by immunofluorescence. The tagged polypeptide was detected at the plasma membrane and in a granular fashion in the perinuclear region, a region dense in ER membranes in Xenopus oocytes (Fig. 1).

Figure 2 shows that the EEEV capsid protein is an inhibitor of gene expression.

In figure 8b, the anti-El" antibody gave a punctal staining pattern which probably represented the endosomal structures

"E1 fusion protein uses first heterodimerization with p62 as a means to become incorporated into the viral envelope and then dissociation from the cleaved p62 (e2), and reorganization, possibly within itself as a way to become activated (Membrane Fusion Process, pg.9)."

See Table 1 of Papaer

Non structural protein (NSP) 1 as a IFN antagonist. See figure 1

in figure 2.(lane 8,9,11,12)). "This suggests that in the absence of E3, the spike glycoproteins do not form heterodimeric complexes at any

time after synthesis"(involved in virus assembly). Lobigs,M. et at.(1990).

Fig-1 shows how 6k makes the cell membrane more permeable by showing the location of tagged polypeptides in two different cells. One affected be the 6k protein and the other not.

In figure 1A, when the expression of NSP3 was silenced in infected cells, the distribution of mRNAs with a poly(A) tail appeared very similar to that observed in uninfected cells, indicating that NSP3 is involved in the nuclear accumulation both of PABPC and of poly(A)-containing mRNAs.

Rubio, R et al. (2013) see PMID reference number