Literature DB >> 2998002

Amino-terminal amino acid sequences of structural proteins of three flaviviruses.

J R Bell, R M Kinney, D W Trent, E M Lenches, L Dalgarno, J H Strauss.   

Abstract

N-terminal amino acid sequences of structural proteins of three flaviviruses, yellow fever, St. Louis encephalitis, and dengue-2 viruses, have been obtained. The glycoproteins of these three viruses are 52-60% conserved in the region sequenced, depending upon which pair of viruses are compared, and 40% of the amino acids are invariant in all three viruses. Thus, flaviviruses are closely related and have in all probability descended from a common ancestor. Furthermore, residues important in the secondary structure of proteins are conserved, suggesting that the overall conformation of the glycoproteins is the same in all three viruses while considerable variation in the primary sequence can be accommodated. The N-terminal regions of the nucleocapsid proteins of yellow fever and St. Louis encephalitis viruses show markedly less homology (25%) and this region is highly basic with one-quarter (yellow fever) or one-third (St. Louis encephalitis) of the residues being lysine or arginine. N-terminal sequences for the M protein of yellow fever and for NV2(GP19) of St. Louis encephalitis viruses are also reported.

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Year:  1985        PMID: 2998002     DOI: 10.1016/0042-6822(85)90110-2

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  16 in total

1.  Fine mapping of a cis-acting sequence element in yellow fever virus RNA that is required for RNA replication and cyclization.

Authors:  Jeroen Corver; Edith Lenches; Kayla Smith; R Aaron Robison; Trisha Sando; Ellen G Strauss; James H Strauss
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

2.  Both nonstructural proteins NS2B and NS3 are required for the proteolytic processing of dengue virus nonstructural proteins.

Authors:  B Falgout; M Pethel; Y M Zhang; C J Lai
Journal:  J Virol       Date:  1991-05       Impact factor: 5.103

3.  Processing of dengue virus type 2 structural proteins containing deletions in hydrophobic domains.

Authors:  A Gruenberg; P J Wright
Journal:  Arch Virol       Date:  1992       Impact factor: 2.574

4.  Processing of the yellow fever virus nonstructural polyprotein: a catalytically active NS3 proteinase domain and NS2B are required for cleavages at dibasic sites.

Authors:  T J Chambers; A Grakoui; C M Rice
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

5.  Maturation of dengue virus nonstructural protein 4B in monocytes enhances production of dengue hemorrhagic fever-associated chemokines and cytokines.

Authors:  James F Kelley; Pakieli H Kaufusi; Esther M Volper; Vivek R Nerurkar
Journal:  Virology       Date:  2011-08-02       Impact factor: 3.616

6.  Cleavage of dengue virus NS1-NS2A requires an octapeptide sequence at the C terminus of NS1.

Authors:  H Hori; C J Lai
Journal:  J Virol       Date:  1990-09       Impact factor: 5.103

7.  In vitro processing of dengue virus structural proteins: cleavage of the pre-membrane protein.

Authors:  L Markoff
Journal:  J Virol       Date:  1989-08       Impact factor: 5.103

Review 8.  The dengue viruses.

Authors:  E A Henchal; J R Putnak
Journal:  Clin Microbiol Rev       Date:  1990-10       Impact factor: 26.132

9.  Processing of yellow fever virus polyprotein: role of cellular proteases in maturation of the structural proteins.

Authors:  A Ruiz-Linares; A Cahour; P Després; M Girard; M Bouloy
Journal:  J Virol       Date:  1989-10       Impact factor: 5.103

10.  Cleavage of the dengue virus polyprotein at the NS3/NS4A and NS4B/NS5 junctions is mediated by viral protease NS2B-NS3, whereas NS4A/NS4B may be processed by a cellular protease.

Authors:  A Cahour; B Falgout; C J Lai
Journal:  J Virol       Date:  1992-03       Impact factor: 5.103

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