Localization of neutralizing epitopes and the receptor-binding site within the amino-terminal 330 amino acids of the murine coronavirus spike protein
By H. Kubo, Yasuko K. Yamada, Fumihiro, Taguchi. 1994
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- S. Weiss
- P. Masters
- Rachel L. Graham
- Ralph S. Baric
- Fang Li
- Xiuyuan Ou
- J. Leibowitz
- Zhaohui Qian
Citations in the corpus
- Recombination, Reservoirs, and the Modular Spike: Mechanisms of Coronavirus Cross-Species Transmission (2009, background): “terminus of S1 (15, 18, 63, 75), suggesting the possibility that these domains were acquired by distinct, disparate recombina-”
- The Molecular Biology of Coronaviruses (2006, background): “By contrast, the RBD of MHV was localized to the amino terminus of the S molecule, amino acids 1–330 (Kubo et al., 1994; Suzuki and Taguchi, 1996; Taguchi, 1995).”
- Coronavirus Pathogenesis and the Emerging Pathogen Severe Acute Respiratory Syndrome Coronavirus (2005, background): “The amino-terminal S1 subunit, which is believed to form the globular head of the mature protein, contains a receptor binding domain (RBD) within the first 330 amino acids (163).”
- Coronavirus Pathogenesis (2011, background): “amino acid of spike (Kubo et al., 1994), which encompasses the NTD described above (Peng et al.”
- What’s new in the renin-angiotensin system? (2004, background): “However, the receptor for another group 2 coronavirus, murine hepatitis virus (MHV), has been identified as a member of the pleiotropic family of carcinoembryonic antigen-cell adhesion molecules (CEACAMs), which are members of the immunoglobulin superfamily [27] [28] [29] [30] .”
- Structure, Function, and Evolution of Coronavirus Spike Proteins (2016, background): “S1-NTDs are responsible for binding sugar (23, 34, 43, 44), with the only known exception being betacoronavirus MHV S1-NTD that recognizes a protein receptor CEACAM1 (45).”
- Identification of the Receptor-Binding Domain of the Spike Glycoprotein of Human Betacoronavirus HKU1 (2015, background): “The 87 first is the N-terminal domain (NTD) that contains the receptor-binding site for 88 murine β-CoV MHV in group A (19) and also binds to sialic-acid containing moieties 89 on host cell membranes for several α-CoVs such as TGEV of swine (26), several 90”