[HTML][HTML] H1 and H7 influenza haemagglutinin structures extend a structural classification of haemagglutinin subtypes
RJ Russell, SJ Gamblin, LF Haire, DJ Stevens, B Xiao… - Virology, 2004 - Elsevier
RJ Russell, SJ Gamblin, LF Haire, DJ Stevens, B Xiao, Y Ha, JJ Skehel
Virology, 2004•ElsevierComparing the structures of H3, H5 and H9 subtype haemagglutinins, we deduced a
structural basis for including all 15 influenza subtypes in four clades. H3, H5 and H9
represent three of these clades; we now report the structure of an H7 HA as a representative
of the fourth clade. We confirm the structure of the turn at the N-terminus of the conserved
central α-helix of HA2, and the combination of ionisable residues near the “fusion peptide”
as clade-specific features. We compare the structures of three H1 HAs with H5 HA in the …
structural basis for including all 15 influenza subtypes in four clades. H3, H5 and H9
represent three of these clades; we now report the structure of an H7 HA as a representative
of the fourth clade. We confirm the structure of the turn at the N-terminus of the conserved
central α-helix of HA2, and the combination of ionisable residues near the “fusion peptide”
as clade-specific features. We compare the structures of three H1 HAs with H5 HA in the …
Comparing the structures of H3, H5 and H9 subtype haemagglutinins, we deduced a structural basis for including all 15 influenza subtypes in four clades. H3, H5 and H9 represent three of these clades; we now report the structure of an H7 HA as a representative of the fourth clade. We confirm the structure of the turn at the N-terminus of the conserved central α-helix of HA2, and the combination of ionisable residues near the “fusion peptide” as clade-specific features. We compare the structures of three H1 HAs with H5 HA in the same clade, to refine our previous classification and we confirm the division of the clades into two groups of two. We also show the roles of carbohydrate side chains in the esterase-fusion domain boundaries in the formation of clade-specific structural markers.
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