(Q30991310)

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Free major histocompatibility complex class I heavy chain is preferentially targeted for degradation by human T-cell leukemia/lymphotropic virus type 1 p12(I) protein

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scholarly article

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Europe PubMed Central

PMC publication ID

13 September 2017

Free major histocompatibility complex class I heavy chain is preferentially targeted for degradation by human T-cell leukemia/lymphotropic virus type 1 p12(I) protein (English)

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Europe PubMed Central

PMC publication ID

13 September 2017

Human T-lymphotropic virus 1

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Vincenzo Ciminale

object named as

V Ciminale

4

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author name string

J M Johnson

1

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Europe PubMed Central

PMC publication ID

13 September 2017

C Nicot

2

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Europe PubMed Central

PMC publication ID

13 September 2017

J Fullen

3

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Europe PubMed Central

PMC publication ID

13 September 2017

L Casareto

5

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Europe PubMed Central

PMC publication ID

13 September 2017

J C Mulloy

6

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Europe PubMed Central

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13 September 2017

S Jacobson

7

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Europe PubMed Central

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13 September 2017

G Franchini

8

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Europe PubMed Central

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13 September 2017

publication date

1 July 2001

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Europe PubMed Central

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13 September 2017

number of pages

9

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Journal of Virology

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Europe PubMed Central

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13 September 2017

75

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Europe PubMed Central

PMC publication ID

13 September 2017

13

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Europe PubMed Central

PMC publication ID

13 September 2017

6086-6094

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Europe PubMed Central

PMC publication ID

13 September 2017

HTLV-1 p12(I) protein enhances STAT5 activation and decreases the interleukin-2 requirement for proliferation of primary human peripheral blood mononuclear cells

1 reference

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1 reference

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Viral subversion of the immune system

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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A lysine-to-arginine change found in natural alleles of the human T-cell lymphotropic/leukemia virus type 1 p12(I) protein greatly influences its stability

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Nef interacts with the mu subunit of clathrin adaptor complexes and reveals a cryptic sorting signal in MHC I molecules

1 reference

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Human T-cell leukemia virus type 1 pX-I and pX-II open reading frames are dispensable for the immortalization of primary lymphocytes

1 reference

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1 reference

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The HIV-1 Nef protein acts as a connector with sorting pathways in the Golgi and at the plasma membrane

1 reference

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Sec61-mediated transfer of a membrane protein from the endoplasmic reticulum to the proteasome for destruction

1 reference

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Protein transport across the eukaryotic endoplasmic reticulum and bacterial inner membranes

1 reference

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Antigen processing and presentation by the class I major histocompatibility complex

1 reference

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The human T-cell leukemia/lymphotropic virus type 1 p12I proteins bind the interleukin-2 receptor beta and gammac chains and affects their expression on the cell surface

1 reference

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The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum to the cytosol

1 reference

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Endocytosis of major histocompatibility complex class I molecules is induced by the HIV–1 Nef protein

1 reference

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1 reference

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The p12I, p13II, and p30II proteins encoded by human T-cell leukemia/lymphotropic virus type I open reading frames I and II are localized in three different cellular compartments.

1 reference

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The human T-cell leukemia/lymphotropic virus type I p12I protein cooperates with the E5 oncoprotein of bovine papillomavirus in cell transformation and binds the 16-kilodalton subunit of the vacuolar H+ ATPase.

1 reference

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1 reference

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Calnexin retains unassembled major histocompatibility complex class I free heavy chains in the endoplasmic reticulum

1 reference

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1 reference

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1 reference

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Human cytomegalovirus down-regulates HLA class I expression by reducing the stability of class I H chains

1 reference

https://pubmed.ncbi.nlm.nih.gov/11390610

12 December 2020

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Identifiers

10.1128/JVI.75.13.6086-6094.2001

1 reference

Europe PubMed Central

PMC publication ID

13 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 September 2017

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