TY - JOUR
T1 - Structure and sequence based functional annotation of Zika virus NS2b protein
T2 - Computational insights
AU - Aguilera-Pesantes, Daniel
AU - Méndez, Miguel A.
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2017/10/28
Y1 - 2017/10/28
N2 - While Zika virus (ZIKV) outbreaks are a growing concern for global health, a deep understanding about the virus is lacking. Here we report a contribution to the basic science on the virus— a detailed computational analysis of the non structural protein NS2b. This protein acts as a cofactor for the NS3 protease (NS3Pro) domain that is important on the viral life cycle, and is an interesting target for drug development. We found that ZIKV NS2b cofactor is highly similar to other virus within the Flavivirus genus, especially to West Nile Virus, suggesting that it is completely necessary for the protease complex activity. Furthermore, the ZIKV NS2b has an important role to the function and stability of the ZIKV NS3 protease domain even when presents a low conservation score. In addition, ZIKV NS2b is mostly rigid, which could imply a non dynamic nature in substrate recognition. Finally, by performing a computational alanine scanning mutagenesis, we found that residues Gly 52 and Asp 83 in the NS2b could be important in substrate recognition.
AB - While Zika virus (ZIKV) outbreaks are a growing concern for global health, a deep understanding about the virus is lacking. Here we report a contribution to the basic science on the virus— a detailed computational analysis of the non structural protein NS2b. This protein acts as a cofactor for the NS3 protease (NS3Pro) domain that is important on the viral life cycle, and is an interesting target for drug development. We found that ZIKV NS2b cofactor is highly similar to other virus within the Flavivirus genus, especially to West Nile Virus, suggesting that it is completely necessary for the protease complex activity. Furthermore, the ZIKV NS2b has an important role to the function and stability of the ZIKV NS3 protease domain even when presents a low conservation score. In addition, ZIKV NS2b is mostly rigid, which could imply a non dynamic nature in substrate recognition. Finally, by performing a computational alanine scanning mutagenesis, we found that residues Gly 52 and Asp 83 in the NS2b could be important in substrate recognition.
KW - Computational alanine scanning mutagenesis
KW - Flavivirus
KW - NS2b
KW - NS3
KW - Protein disorder
KW - Transmembrane domains
KW - Zika virus
UR - http://www.scopus.com/inward/record.url?scp=85012912360&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2017.02.035
DO - 10.1016/j.bbrc.2017.02.035
M3 - Artículo
C2 - 28188791
AN - SCOPUS:85012912360
SN - 0006-291X
VL - 492
SP - 659
EP - 667
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -