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Volume 11, Number 7—July 2005
Research

Human Metapneumovirus Genetic Variability, South Africa

Herbert P. Ludewick*, Yacine Abed†, Nadia van Niekerk*, Guy Boivin†, Keith P. Klugman*‡, and Shabir A. Madhi*Comments to Author 
Author affiliations: *University of the Witwatersrand, Johannesburg, South Africa; †Laval University, Quebec City, Quebec, Canada; ‡Emory University, Atlanta, Georgia, USA

Main Article

Figure A1

Alignment of the G proteins of representative samples of South African human metapneumovirus (hMPV) isolates and prototypes sequences from the Netherlands (NL/1/00, NL/1/99, NL/1/94, and NL/17/00) and Canada (hMPV13-00, CAN97-83, hMPV33-01, and CAN75-98). Only amino acid residues that differed from the Netherlands' prototypes for each subgroup are shown. Identical amino acids are represented by periods; dashes indicate gaps. Arrows above the alignment indicate the proposed intracellular, transme

Figure A1. . . Alignment of the G proteins of representative samples of South African human metapneumovirus (hMPV) isolates and prototypes sequences from the Netherlands (NL/1/00, NL/1/99, NL/1/94, and NL/17/00) and Canada (hMPV13-00, CAN97-83, hMPV33-01, and CAN75-98). Only amino acid residues that differed from the Netherlands' prototypes for each subgroup are shown. Identical amino acids are represented by periods; dashes indicate gaps. Arrows above the alignment indicate the proposed intracellular, transmembrane and extracellular domains. Potential N-linked glycosylation sites are underlined. Numbers indicate the amino acid position in the G open reading frames corresponding to the Netherlands' prototype isolates. Download PDF [46 KB, 5 pages].

Main Article

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