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. 2016 May 12;5(2):38–62. doi: 10.5501/wjv.v5.i2.38

Table 1.

Cell surface molecules interacting with rotavirus structural proteins during entry

Cellular molecule Rotavirus protein Activity Viral protein motif involved Ref.
Sialic acid VP8* Binding Carbohydrate binding site [108]
α2β1 VP5* Post-binding DGE (VP5*) [106]
α4β1 VP7, VP5* Post-binding YGL (VP5*); LDV o LDI (VP7) [11,121]
αxβ2 VP7 Post-binding GPR (VP7) [114,121]
αvβ3 VP7 Post-binding, oxidoreduction 161NEWLCNPMD169 [10,113]
Hsc70 VP5*, VP7, VP6 Chaperoning aa 642-658 (VP5*); aa 280-296 (VP6); aa 531-554 (VP5*) [8,103]
PDI VP5*, VP7, VP6 Chaperoning, oxidoreduction aa 200-219 (VP4); aa 189-210 and aa 243-263 (VP7) [12,94, Rivera M, Guerrero CA, Acosta O, manuscript in preparation]
HBGAs VP8* Binding Carbohydrate binding site [111]

Hsc70: Heat shock cognate protein 70; PDI: Protein disulfide isomerase; HBGAs: Histo-blood group antigens.