Structural and molecular evidence suggesting coronavirus-driven evolution of mouse receptor

Journal of Biological Chemistry

Volumn 292, Issue 6, 2017, Pages 2174-2181

  Peng, Guiqing ^a,b   Yang, Yang ^a   Pasquarella, Joseph R ^a   Xu, Liqing ^a,b   Qian, Zhaohui ^c,d   Holmes, Kathryn V ^d   Li, Fang ^a  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^b HUAZHONG AGRICULTURAL UNIVERSITY   (China)

^c INSTITUTE OF PATHOGEN BIOLOGY   (China)

^d UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMISTRY; CRYSTAL STRUCTURE; PATHOGENS; PROTEINS;

BETA-STRAND; CORONAVIRUSES; MOLECULAR MECHANISM; PROTEIN-PROTEIN BINDING; RECEPTOR ACTIVITY; RECEPTOR PROTEINS; STRUCTURAL DIFFERENCES;

MAMMALS;

MURINE HEPATITIS VIRUS RECEPTOR; UNCLASSIFIED DRUG; VIRUS RECEPTOR; CARCINOEMBRYONIC ANTIGEN; CEACAM1 PROTEIN, MOUSE;

ARTICLE; BINDING AFFINITY; BINDING SITE; CEACAM1A GENE; CEACAM1B GENE; CONTROLLED STUDY; CORONAVIRUS INFECTION; CRYSTAL STRUCTURE; GENE FREQUENCY; GENE FUNCTION; GENE IDENTIFICATION; GENETIC VARIATION; MOLECULAR DYNAMICS; MOLECULAR EVOLUTION; MURINE HEPATITIS VIRUS; NONHUMAN; PROTEIN DETERMINATION; PROTEIN FUNCTION; PROTEIN STRUCTURE; RESIDUE ANALYSIS; SEQUENCE ANALYSIS; STRUCTURE ANALYSIS; VIRUS ATTACHMENT; VIRUS GENE; AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; MEMBRANE FUSION; METABOLISM; MOUSE; MUTATION; PHYSIOLOGY; PROTEIN CONFORMATION; SEQUENCE HOMOLOGY; X RAY CRYSTALLOGRAPHY;

AMINO ACID SEQUENCE; ANIMALS; BINDING SITES; CARCINOEMBRYONIC ANTIGEN; CRYSTALLOGRAPHY, X-RAY; MEMBRANE FUSION; MICE; MURINE HEPATITIS VIRUS; MUTATION; PROTEIN CONFORMATION; RECEPTORS, VIRUS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 85012050954     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M116.764266     Document Type: Article

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