Detailed entry information

Protein Information (annotations from UniProt)

Database IDHIV0012231
UniProt IDP01920
Primary gene name(s)HLA-DQB1
Synonym gene name(s)HLA-DQB
Protein nameHLA class II histocompatibility antigen, DQ beta 1 chain
Protein functionBinds peptides derived from antigens that access the endocytic route of antigen presenting cells, APC and presents them on the cell surface for recognition by the CD4 T-cells. The peptide binding cleft accommodates peptides of 10-30 residues. The peptides presented by MHC class II molecules are generated mostly by degradation of proteins that access the endocytic route, where they are processed by lysosomal proteases and other hydrolases. Exogenous antigens that have been endocytosed by the APC are thus readily available for presentation via MHC II molecules, and for this reason this antigen presentation pathway is usually referred to as exogenous. As membrane proteins on their way to degradation in lysosomes as part of their normal turn-over are also contained in the endosomal/lysosomal compartments, exogenous antigens must compete with those derived from endogenous components. Autophagy is also a source of endogenous peptides, autophagosomes constitutively fuse with MHC class II loading compartments. In addition to APCs, other cells of the gastrointestinal tract, such as epithelial cells, express MHC class II molecules and CD74 and act as APCs, which is an unusual trait of the GI tract. To produce a MHC class II molecule that presents an antigen, three MHC class II molecules, heterodimers of an alpha and a beta chain associate with a CD74 trimer in the ER to form a heterononamer. Soon after the entry of this complex into the endosomal/lysosomal system where antigen processing occurs, CD74 undergoes a sequential degradation by various proteases, including CTSS and CTSL, leaving a small fragment termed CLIP, class-II-associated invariant chain peptide. The removal of CLIP is facilitated by HLA-DM via direct binding to the alpha-beta-CLIP complex so that CLIP is released. HLA-DM stabilizes MHC class II molecules until primary high affinity antigenic peptides are bound. The MHC II molecule bound to a peptide is then transported to the cell membrane surface. In B-cells, the interaction between HLA-DM and MHC class II molecules is regulated by HLA-DO. Primary dendritic cells, DCs also to express HLA-DO. Lysosomal microenvironment has been implicated in the regulation of antigen loading into MHC II molecules, increased acidification produces increased proteolysis and efficient peptide loading.
Subcellular locationCell membrane;
Single-pass type I membrane protein. Endoplasmic reticulum membrane;
Single-pass type I membrane protein. Golgi apparatus, trans-Golgi network membrane;
Single-pass type I membrane protein. Endosome membrane;
Single-pass type I membrane protein. Lysosome membrane;
Single-pass type I membrane protein. Note=The MHC class II complex transits through a number of intracellular compartments in the endocytic pathway until it reaches the cell membrane for antigen presentation.
ECO codeClick here for more information.
Amino acid sequence
FASTA format: P01920
Gene Ontology
(Biological Process)
Complete annatation
antigen processing and presentation of exogenous peptide antigen via MHC class II [GO:0019886];
humoral immune response mediated by circulating immunoglobulin [GO:0002455];
immune response [GO:0006955];
immunoglobulin production involved in immunoglobulin mediated immune response [GO:0002381];
interferon-gamma-mediated signaling pathway [GO:0060333];
T cell costimulation [GO:0031295];
T cell receptor signaling pathway [GO:0050852]
Gene Ontology
(Molecular Function)
Complete annatation
MHC class II receptor activity [GO:0032395];
peptide antigen binding [GO:0042605]
Gene Ontology
(Cellular Component)
Complete annatation
clathrin-coated endocytic vesicle membrane [GO:0030669];
endocytic vesicle membrane [GO:0030666];
endosome membrane [GO:0010008];
ER to Golgi transport vesicle membrane [GO:0012507];
Golgi membrane [GO:0000139];
integral component of lumenal side of endoplasmic reticulum membrane [GO:0071556];
lysosomal membrane [GO:0005765];
membrane [GO:0016020];
MHC class II protein complex [GO:0042613];
plasma membrane [GO:0005886];
trans-Golgi network membrane [GO:0032588];
transport vesicle membrane [GO:0030658]
Protein-protein interactionunknown
Phylogenetic treeP01920
HIV replication factor status Zhou et al., Cell. Host. Microbe., 2008
Brass et al., Science, 2008
Smith et al., J. Immunol, 2010
gene status
Lu et al., J. Virol., 2011
      Folds changes 8h: unknown; Folds changes 16h: unknown; Tested: unknown;
Schoggins JW and Rice CM, Curr. Opin. Virol., 2011
      Targeted viruses: unknown
      Viral life cycle: unknown
      Mechanism related to antiviral activity: unknown
Anti-viral restriction factor Liu et al., Retrovirology, 2011
      unknown (Triplicates)

Gene Expression Profile       top

            Up-regulated;            Down-regulated

For brief introduction to each study, please go to the help page.

Gene expression during HIV latency

(1). Mohammadi et al., PLoS Pathog., 2014

Differentially expressed transcripts (Pairwise) during latency and subsequent viral reactivation using several agents - Primary CD4+ T-cell based model

DMSO: Dimethyl suloxyde (negative control) - 0.0033% final
SAHA: Vorinostat (Histone deacetylase inhibitor) - 0.5 μM
CD3: TCR Stimulation by IL-2+ antiCD3/anti-CD28 antibodies
IL7: Interleukin-7 based stimulation
DISU: Disulfiram (alcohol dehydrogenase inhibitor) - 0.5 μM
AZA: 5-azacytidine (AZA; DNA methylation inhibitor) - 1 μM
Experimental Condition Log2 Fold Change P value Adjusted P value
AZA vs. CD3-0.7987797515424840.2312705417491260.341484192277582
AZA vs. DISU0.01487596896026950.9532744074990450.996649735504266
AZA vs. IL7-0.2936653955527020.1521337355364450.919820214898048
AZA vs. SAHA1.068377873323670.000161100463819230.00537262918498026
DISU vs. CD30.8016838714439050.2290338457652890.353047979452497
DISU vs. IL7-0.3186916363414780.2083291238849240.58729666698644
DISU vs. SAHA1.057014162744420.0003461145812032610.00962708962373402
DMSO vs. AZA-0.02794371131453180.8930994342355041
DMSO vs. CD30.7613664957775020.2441145606781870.34904765909388
DMSO vs. DISU-0.0441096750445130.8570489836062310.983807945138555
DMSO vs. IL7-0.2586618849299180.1545871482760010.659331158124528
DMSO vs. SAHA1.091371198697167.71131822696614e-060.000464869107994426
HIV vs. Mock in Activation-0.2085129929967480.875888582457390.999983755607037
HIV vs. Mock in Latency0.3916083673641220.01840698411894060.495488708861649
IL7 vs. CD30.5093775359363750.4336123124913120.568877916805775
SAHA vs. CD31.844384485463260.005869492569014370.0163469327324056
SAHA vs. IL71.361174896521555.05821683427499e-083.71939319804201e-06
(2). Iglesias-Ussel et al., J. Virol., 2013

Up and Downregulated transcripts during Latency (Latently infected CD4+ T cells vs Uninfected)- Primary CD4+Tcell based model
Log2 Fold Change P Value
unknown unknown

Gene expression during HIV infection and replication

(1). Imbeault et al., PloS Pathog., 2012

Transcriptomic profiling of HIV-1 infected CD4+ T cells - Primary CD4+ T cells
Experiment type Log2 Fold Change P Value Adjusted P Value
Infected vs. Mock unknown unknown unknown
Infected vs. Bystander unknown unknown unknown
(2). Lefebvre et al., J. Virol., 2011

Transcriptome analysis of T-cell line (Sup T1)
Log2 Fold Change unknown
(3). Li et al., J. Immunol., 2013

Lymphatic tissue
Acute Fold Change Acute P Value Asymt Fold Change Asypt P Value AIDS Fold Change AIDS P Value
unknown unknown unknown unknown unknown unknown
(4). Chang et al., MBio., 2011

Transcriptome analysis of T-cell line (Sup T1)

Derived from Sherrill-Mix et al., BMC Retrovirol., 2015 cross validation
Up-regulated (True) unknown
(5). Sherrill-Mix et al., BMC Retrovirol., 2015

Deep RNA-seq analysis of primary human T cell infected with low passage HIV isolate HIV89.6 - Primary CD4+ T cell based
Test Status Log2 Fold Change P Value
OK 0.794539 0.000305467
(6). Rotger et al., PLoS Pathog., 2010

Genome-wide mRNA expression of CD4+ T cells from HIV-infected patient
(Genes differentially expressed (at adjusted p<0.01) according to the empirical Bayes approach)
Log2 Fold Change P Value
unknown unknown

Proteomic/Transcriptomics studies indicating differentially expressed genes mediated by HIV

(1). Greenwood et al., Elife, 2016

Activated (CD3/CD28) Primary human CD4+ T cells infected with pNL4-3-dE-EGFP. The table shows the complete (unfiltered) TMT (tandem mass tag)-based proteomic time course dataset
6 h 24 h 48 h 72 h RTi
unknown unknown unknown unknown unknown
(2). Navare et al., Virology, 2012

SUP-T1 cell line
FC-4hpi P-value FC-8hpi P-value FC-20hpi P-value Category
unknown unknown unknown unknown unknown unknown unknown
(3). Hyrcza et al., J. Virolo., 2007

Primary human CD4+ and CD8+ T Cells
Affymetrix Prob ID Fold Change In CD8? Category
unknown unknown unknown unknown

Protein Overview       top

Drug-protein Interaction       (annotations from DrugBank)      top

Drugbank ID Drug Name Drug Status Pharmacological Action Drug Action
DB00071 Insulin Pork approved unknown unknown

Protein Secondary Structure       (annotations from PDB)      top

PDB Accession Method Resolution Chain Structure Preview
1JK8 X-ray 2.4Å B=35-224.
1NBN Model - B=35-224.
1S9V X-ray 2.2Å B/E=33-230.
1UVQ X-ray 1.8Å B=35-230.
2NNA X-ray 2.1Å B=33-224.
4GG6 X-ray 3.2Å B/D=33-224.
4OZF X-ray 2.7Å B=33-224.
4OZG X-ray 3.0Å B/D=33-224.
4OZH X-ray 2.8Å B/D=33-224.
4OZI X-ray 3.2Å B/D=33-224.

HIV-1 Interaction       (annotations from NCBI HIV-1 Interaction Database)      top

HIV Partner Interaction Type PubMed
Pr55(Gag) upregulates 18945465
Envelope transmembrane glycoprotein gp41 incorporates 10729169
Envelope surface glycoprotein gp120 interacts with 1978941
Envelope surface glycoprotein gp160; precursor associates with 3489470
Nef inhibits 11593029
Nef downregulates 12970439
Pr55(Gag) regulated by 22860026
Tat downregulates 10661406
Vif downregulates 23333304
Vpu modulates 17959659
Envelope transmembrane glycoprotein gp41 upregulates 8084338
Envelope surface glycoprotein gp120 inhibits 2543930

Metabolic/Signalling Pathway       (annotations from KEGG database)      top

Pathway Accession Number Description
hsa04145 Phagosome - Homo sapiens (human)
hsa04514 Cell adhesion molecules (CAMs) - Homo sapiens (human)
hsa04612 Antigen processing and presentation - Homo sapiens (human)
hsa04640 Hematopoietic cell lineage - Homo sapiens (human)
hsa04658 Th1 and Th2 cell differentiation - Homo sapiens (human)
hsa04659 Th17 cell differentiation - Homo sapiens (human)
hsa04672 Intestinal immune network for IgA production - Homo sapiens (human)
hsa04940 Type I diabetes mellitus - Homo sapiens (human)
hsa05140 Leishmaniasis - Homo sapiens (human)
hsa05145 Toxoplasmosis - Homo sapiens (human)
hsa05150 Staphylococcus aureus infection - Homo sapiens (human)
hsa05152 Tuberculosis - Homo sapiens (human)
hsa05164 Influenza A - Homo sapiens (human)
hsa05166 HTLV-I infection - Homo sapiens (human)
hsa05168 Herpes simplex infection - Homo sapiens (human)
hsa05169 Epstein-Barr virus infection - Homo sapiens (human)
hsa05310 Asthma - Homo sapiens (human)
hsa05320 Autoimmune thyroid disease - Homo sapiens (human)
hsa05321 Inflammatory bowel disease (IBD) - Homo sapiens (human)
hsa05322 Systemic lupus erythematosus - Homo sapiens (human)
hsa05323 Rheumatoid arthritis - Homo sapiens (human)
hsa05330 Allograft rejection - Homo sapiens (human)
hsa05332 Graft-versus-host disease - Homo sapiens (human)
hsa05416 Viral myocarditis - Homo sapiens (human)