Serveur d'exploration H2N2

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Complete sequence analysis shows that the hemagglutinins of the H0 and H2 subtypes of human influenza virus are closely related

Identifieur interne : 002736 ( Main/Exploration ); précédent : 002735; suivant : 002737

Complete sequence analysis shows that the hemagglutinins of the H0 and H2 subtypes of human influenza virus are closely related

Auteurs : Alan L. Hiti [États-Unis] ; Alan R. Davis [États-Unis] ; Debi P. Nayak [États-Unis]

Source :

RBID : ISTEX:A2B617D5D1EC0469BCD056090823D1A2768E496E

English descriptors

Abstract

Abstract: The complete sequence of the hemagglutinin (HA) gene from the A/WSN/33 strain (H0N1) of human influenza virus has been determined and compared with four other HA sequences: the human H2 strain A/Japan/305/57, the avian Havl strain A/FPV/Rostock/34, and the human H3 strains A/Memphis/102/72 and A/Victoria/3/75. The A/WSN HA gene is 1775 nucleotides in length coding for 565 amino acids. The plus strand sequence contains a noncoding region of 32 nucleotides at the 5′ end followed by the coding region of 1695 nucleotides and a 3′ noncoding region of 48 nucleotides (including the UGA nonsense codon). The amino acid sequence derived from the nucleotide sequence shows the presence of a 17 amino acid long “signal” prepeptide at the amino terminus followed by an HA1 of 325 amino acids, a single arginine connecting residue, and an HA2 of 222 residues at the carboxy terminus. The comparison with other subtypes reveals many conserved features throughout the primary sequence in all strains and reinforces the argument for a basic architecture required of the entire hemagglutinin molecule. Comparison of the H0 and H2 HAs (minus the “signal” prepeptide) shows a 67% amino acid sequence homology, which is the highest among the subtypes, suggesting a close geneologic relationship between the two.

Url:
DOI: 10.1016/0042-6822(81)90658-9


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title>Complete sequence analysis shows that the hemagglutinins of the H0 and H2 subtypes of human influenza virus are closely related</title>
<author>
<name sortKey="Hiti, Alan L" sort="Hiti, Alan L" uniqKey="Hiti A" first="Alan L." last="Hiti">Alan L. Hiti</name>
</author>
<author>
<name sortKey="Davis, Alan R" sort="Davis, Alan R" uniqKey="Davis A" first="Alan R." last="Davis">Alan R. Davis</name>
</author>
<author>
<name sortKey="Nayak, Debi P" sort="Nayak, Debi P" uniqKey="Nayak D" first="Debi P." last="Nayak">Debi P. Nayak</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:A2B617D5D1EC0469BCD056090823D1A2768E496E</idno>
<date when="1981" year="1981">1981</date>
<idno type="doi">10.1016/0042-6822(81)90658-9</idno>
<idno type="url">https://api.istex.fr/ark:/67375/6H6-5NTZH3SW-8/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000741</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000741</idno>
<idno type="wicri:Area/Istex/Curation">000741</idno>
<idno type="wicri:Area/Istex/Checkpoint">001368</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001368</idno>
<idno type="wicri:doubleKey">0042-6822:1981:Hiti A:complete:sequence:analysis</idno>
<idno type="wicri:Area/Main/Merge">002881</idno>
<idno type="wicri:Area/Main/Curation">002736</idno>
<idno type="wicri:Area/Main/Exploration">002736</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a">Complete sequence analysis shows that the hemagglutinins of the H0 and H2 subtypes of human influenza virus are closely related</title>
<author>
<name sortKey="Hiti, Alan L" sort="Hiti, Alan L" uniqKey="Hiti A" first="Alan L." last="Hiti">Alan L. Hiti</name>
<affiliation wicri:level="1">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, California 90024</wicri:regionArea>
<wicri:noRegion>California 90024</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Davis, Alan R" sort="Davis, Alan R" uniqKey="Davis A" first="Alan R." last="Davis">Alan R. Davis</name>
<affiliation wicri:level="1">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, California 90024</wicri:regionArea>
<wicri:noRegion>California 90024</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Nayak, Debi P" sort="Nayak, Debi P" uniqKey="Nayak D" first="Debi P." last="Nayak">Debi P. Nayak</name>
<affiliation wicri:level="1">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, California 90024</wicri:regionArea>
<wicri:noRegion>California 90024</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Virology</title>
<title level="j" type="abbrev">YVIRO</title>
<idno type="ISSN">0042-6822</idno>
<imprint>
<publisher>ELSEVIER</publisher>
<date type="published" when="1981">1981</date>
<biblScope unit="volume">111</biblScope>
<biblScope unit="issue">1</biblScope>
<biblScope unit="page" from="113">113</biblScope>
<biblScope unit="page" to="124">124</biblScope>
</imprint>
<idno type="ISSN">0042-6822</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0042-6822</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="Teeft" xml:lang="en">
<term>Acid sequence</term>
<term>Aiwsn</term>
<term>Amino</term>
<term>Amino acid</term>
<term>Amino acid sequence</term>
<term>Amino acid sequence homology</term>
<term>Amino acid sequences</term>
<term>Amino acids</term>
<term>Antigenic</term>
<term>Antigenic drift</term>
<term>Arginine</term>
<term>Basic architecture</term>
<term>Carboxy terminus</term>
<term>Cleavage</term>
<term>Codon</term>
<term>Compans</term>
<term>Complete nucleotide sequence</term>
<term>Cysteine</term>
<term>Disulfide</term>
<term>Dopheide</term>
<term>Elsevier</term>
<term>Gething</term>
<term>Havl</term>
<term>Hemagglutinin</term>
<term>Hemagglutinin gene</term>
<term>High degree</term>
<term>Homology</term>
<term>Human influenza virus</term>
<term>Influenza</term>
<term>Influenza virus</term>
<term>Influenza virus hemagglutinin</term>
<term>Laver</term>
<term>Mdbk cells</term>
<term>Nayak</term>
<term>Noncoding region</term>
<term>Nucleotide</term>
<term>Nucleotide sequence</term>
<term>Other honl strains</term>
<term>Other subtypes</term>
<term>Pairing</term>
<term>Polypeptide</term>
<term>Prepeptide</term>
<term>Proteolytic cleavage</term>
<term>Skehel</term>
<term>Subtype pairings</term>
<term>Subtypes</term>
<term>Virology</term>
<term>Virus</term>
<term>Waterfield</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: The complete sequence of the hemagglutinin (HA) gene from the A/WSN/33 strain (H0N1) of human influenza virus has been determined and compared with four other HA sequences: the human H2 strain A/Japan/305/57, the avian Havl strain A/FPV/Rostock/34, and the human H3 strains A/Memphis/102/72 and A/Victoria/3/75. The A/WSN HA gene is 1775 nucleotides in length coding for 565 amino acids. The plus strand sequence contains a noncoding region of 32 nucleotides at the 5′ end followed by the coding region of 1695 nucleotides and a 3′ noncoding region of 48 nucleotides (including the UGA nonsense codon). The amino acid sequence derived from the nucleotide sequence shows the presence of a 17 amino acid long “signal” prepeptide at the amino terminus followed by an HA1 of 325 amino acids, a single arginine connecting residue, and an HA2 of 222 residues at the carboxy terminus. The comparison with other subtypes reveals many conserved features throughout the primary sequence in all strains and reinforces the argument for a basic architecture required of the entire hemagglutinin molecule. Comparison of the H0 and H2 HAs (minus the “signal” prepeptide) shows a 67% amino acid sequence homology, which is the highest among the subtypes, suggesting a close geneologic relationship between the two.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
</list>
<tree>
<country name="États-Unis">
<noRegion>
<name sortKey="Hiti, Alan L" sort="Hiti, Alan L" uniqKey="Hiti A" first="Alan L." last="Hiti">Alan L. Hiti</name>
</noRegion>
<name sortKey="Davis, Alan R" sort="Davis, Alan R" uniqKey="Davis A" first="Alan R." last="Davis">Alan R. Davis</name>
<name sortKey="Nayak, Debi P" sort="Nayak, Debi P" uniqKey="Nayak D" first="Debi P." last="Nayak">Debi P. Nayak</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/H2N2V1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002736 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002736 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    H2N2V1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:A2B617D5D1EC0469BCD056090823D1A2768E496E
   |texte=   Complete sequence analysis shows that the hemagglutinins of the H0 and H2 subtypes of human influenza virus are closely related
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Apr 14 19:59:40 2020. Site generation: Thu Mar 25 15:38:26 2021