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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 02 Nov 2015.

Myosin IG

HA2, K32
MYO1G is a plasma membrane-associated class I myosin (see MIM 601478) that is abundant in T and B lymphocytes and mast cells (Pierce et al., 2001 [PubMed 11544309]; Patino-Lopez et al., 2010 [PubMed 20071333]).[supplied by OMIM, Jun 2010] (from NCBI)
Top mentioned proteins: AE1, ACID, CAN, HAD, CD45
Papers on HA2
New capillary gel electrophoresis method for fast and accurate identification and quantification of multiple viral proteins in influenza vaccines.
Sänger-van de Griend et al., Leiden, Netherlands. In Talanta, 01 Dec 2015
The final method was validated and showed good performance for hemagglutinin fragment 1 (HA1), hemagglutinin fragment 2 (HA2), matrix protein (M) and nucleoprotein (NP).
A Unique Multibasic Proteolytic Cleavage Site and Three Mutations in the HA2 Domain Confer High Virulence of H7N1 Avian Influenza Virus in Chickens.
Mettenleiter et al., Greifswald, Germany. In J Virol, 21 Nov 2015
While Lp with a multibasic cleavage site (Lp_CS445) was less virulent than Hp, full virulence was exhibited when HA2 was substituted by that of Hp.
Development of single-chain variable fragments (scFv) against influenza virus targeting hemagglutinin subunit 2 (HA2).
Chang et al., Taipei, Taiwan. In Arch Virol, 08 Nov 2015
The Tomlinson I and J scFv phage display libraries were screened against the recombinant HA2 protein (rHA2) for three rounds.
Cross-protection of Lactococcus lactis-displayed HA2 subunit against homologous and heterologous influenza A viruses in mice.
Ouyang et al., Chengdu, China. In Arch Virol, 11 Oct 2015
The highly conserved HA2 subunit is a promising candidate for developing a universal influenza vaccine.
New influenza A Virus Entry Inhibitors Derived from the Viral Fusion Peptides.
He et al., Guangzhou, China. In Plos One, Dec 2014
By employing pseudovirus-based entry inhibition assays including H5N1 influenza A virus (IAV), and VSV-G, the mechanism study indicated that the antiviral activity may be associated with the interactions between the HA2 subunit and pFP, of which, the nascent pFP exerted a strong effect to interrupt the conformational changes of HA2, thereby blocking the entry of viruses into host cells.
[Advances in research and development of universal influenza vaccines].
He et al., In Bing Du Xue Bao, 2014
This review describes the research progress in conserved epitopes of influenza virus, the advances in the research and development of universal influenza vaccines based on the relatively conserved sequences of NP, M2e, HA2, and headless HA, the mechanisms of cross-protection, and the methods to improve cross-protection.
New vaccines against influenza virus.
Kang et al., Atlanta, United States. In Clin Exp Vaccine Res, 2014
The strategies of universal vaccines include the matrix 2 protein, the hemagglutinin HA2 stalk domain, and T cell-based multivalent antigens.
Influenza virus hemagglutinin as a vaccine antigen produced in bacteria.
Sączyńska, Warsaw, Poland. In Acta Biochim Pol, 2013
The vast majority of bacterial HAs have been based on the HA1 subunit of HA expressed separately or as a component of conjugate vaccines, but those based on the ectodomain and the HA2 subunit have also been reported.
Protective immunity based on the conserved hemagglutinin stalk domain and its prospects for universal influenza vaccine development.
Rajput et al., Delhi, India. In Biomed Res Int, 2013
Its HA2 subunit (stem domain) is most conserved as compared to HA1 subunit (globular head domain).
Structural biology of the influenza virus fusion peptide.
Worch, Warsaw, Poland. In Acta Biochim Pol, 2013
The fusion is mediated by the influenza hemagglutinin protein (HA), in particular by the fusion peptide (HAfp) located in the N-terminal fragment of HA2 subunit.
DDX1, DDX21, and DHX36 helicases form a complex with the adaptor molecule TRIF to sense dsRNA in dendritic cells.
Liu et al., Houston, United States. In Immunity, 2011
Although DDX1 bound poly I:C via its Helicase A domain, DHX36 and DDX21 bound the TIR domain of TRIF via their HA2-DUF and PRK domains, respectively.
Minor histocompatibility antigen HA-1 and HA-2 polymorphisms in Taiwan: frequency and application in hematopoietic stem cell transplantation.
Yang et al., Taipei, Taiwan. In Clin Chem Lab Med, 2010
the information on allele and genotype frequencies of HA-1 and HA-2 in a Taiwanese population
Myosin 1G is an abundant class I myosin in lymphocytes whose localization at the plasma membrane depends on its ancient divergent pleckstrin homology (PH) domain (Myo1PH).
Shaw et al., Bethesda, United States. In J Biol Chem, 2010
Myosin 1G is an abundant class I myosin in lymphocytes whose localization at the plasma membrane depends on its ancient divergent pleckstrin homology (PH) domain
Mismatch for the minor histocompatibility antigen HA-2 and GVHD occurrence in HLA-A*0201-positive Tunisian recipients of HSCs.
Hmida et al., Tunisia. In Immunol Invest, 2009
gene polymorphism does not have any significant effect on the occurrence of GVHD in Tunisia
Antibody recognition of a highly conserved influenza virus epitope.
Wilson et al., Los Angeles, United States. In Science, 2009
In contrast to other structurally characterized influenza antibodies, CR6261 recognizes a highly conserved helical region in the membrane-proximal stem of HA1 and HA2.
Transducible TAT-HA fusogenic peptide enhances escape of TAT-fusion proteins after lipid raft macropinocytosis.
Dowdy et al., San Diego, United States. In Nat Med, 2004
Using this information, we developed a transducible, pH-sensitive, fusogenic dTAT-HA2 peptide that markedly enhanced TAT-Cre escape from macropinosomes.
In situ dissection of the graft-versus-host activities of cytotoxic T cells specific for minor histocompatibility antigens.
Goulmy et al., Newcastle upon Tyne, United Kingdom. In Nat Med, 2002
Therefore, using a skin-explant assay we investigated the in situ activities of cytotoxic T lymphocytes (CTLs) specific for the ubiquitously expressed mHag H-Y and for the hematopoietic-restricted mHags HA-1 and HA-2.
Atomic structure of the ectodomain from HIV-1 gp41.
Wiley et al., Boston, United States. In Nature, 1997
These features, and the existence of a similar reversal of chain direction in the fusion pH-induced conformation of influenza virus HA2 and in the transmembrane subunit of Moloney murine leukaemia virus (Fig. 1a-d), suggest a common mechanism for initiating fusion.
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