Summary: Class II histocompatibility antigen, beta domain
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Class II histocompatibility antigen, beta domain Provide feedback
No Pfam abstract.
Literature references
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Stern LJ, Brown JH, Jardetzky TS, Gorga JC, Urban RG, Strominger JL, Wiley DC; , Nature 1994;368:215-221.: Crystal structure of the human class II MHC protein HLA-DR1 complexed with an influenza virus peptide. PUBMED:8145819 EPMC:8145819
External database links
| HOMSTRAD: | MHC_II_N MHC_II_beta_NC |
| PANDIT: | PF00969 |
| Pseudofam: | PF00969 |
| SCOP: | 1seb |
| SYSTERS: | MHC_II_beta |
This tab holds annotation information from the InterPro database.
InterPro entry IPR000353
Major Histocompatibility Complex (MHC) glycoproteins are heterodimeric cell surface receptors that function to present antigen peptide fragments to T cells responsible for cell-mediated immune responses. MHC molecules can be subdivided into two groups on the basis of structure and function: class I molecules present intracellular antigen peptide fragments (~10 amino acids) on the surface of the host cells to cytotoxic T cells; class II molecules present exogenously derived antigenic peptides (~15 amino acids) to helper T cells. MHC class I and II molecules are assembled and loaded with their peptide ligands via different mechanisms. However, both present peptide fragments rather than entire proteins to T cells, and are required to mount an immune response.
Class II MHC glycoproteins are expressed on the surface of antigen-presenting cells (APC), including macrophages, dendritic cells and B cells. MHC II proteins present peptide antigens that originate extracellularly from foreign bodies such as bacteria. Proteins from the pathogen are degraded into peptide fragments within the APC, which sequesters these fragments into the endosome so they can bind to MHC class II proteins, before being transported to the cell surface. MHC class II receptors display antigens for recognition by helper T cells (stimulate development of B cell clones) and inflammatory T cells (cause the release of lymphokines that attract other cells to site of infection) [PUBMED:15120183].
MHC class II molecules are comprised of two membrane-spanning chains, alpha and beta, of similar size. Both chains consist of two globular domains (N- and C-terminal), and a transmembrane segment to anchor them to the membrane [PUBMED:7612235]. A groove in the structure acts as the peptide-binding site.
This entry represents the N-terminal domain (also called beta-1 domain) of the beta chain.
More information about these proteins can be found at Protein of the Month: MHC [PUBMED:].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | membrane (GO:0016020) |
| MHC class II protein complex (GO:0042613) | |
| Biological process | antigen processing and presentation (GO:0019882) |
| immune response (GO:0006955) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Pfam Clan
This family is a member of clan MHC (CL0343), which contains the following 4 members:
MHC_I MHC_I_2 MHC_II_alpha MHC_II_betaAlignments
We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database using the family HMM. We also generate alignments using four representative proteomes (RP) sets, the NCBI sequence database, and our metagenomics sequence database. More...
View options
We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.
| Seed (121) |
Full (17595) |
Representative proteomes | NCBI (16212) |
Meta (0) |
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| RP15 (23) |
RP35 (41) |
RP55 (74) |
RP75 (215) |
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| PP/heatmap | 1 | |||||||
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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not generated,
— not available.
Format an alignment
Download options
We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.
| Seed (121) |
Full (17595) |
Representative proteomes | NCBI (16212) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (23) |
RP35 (41) |
RP55 (74) |
RP75 (215) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER3.
HMM logo
HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...
Trees
This page displays the phylogenetic tree for this family's seed alignment. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed alignment.
Note: You can also download the data file for the tree.
Curation and family details
This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.
Curation
| Seed source: | Pfam-B_331 (release 3.0) |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Finn RD, Bateman A, Griffiths-Jones SR |
| Number in seed: | 121 |
| Number in full: | 17595 |
| Average length of the domain: | 69.80 aa |
| Average identity of full alignment: | 52 % |
| Average coverage of the sequence by the domain: | 67.66 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 75 | ||||||||||||
| Family (HMM) version: | 14 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Sunburst controls
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Interactions
There are 6 interactions for this family. More...
MA-Mit C1-set DUF1968 MHC_II_beta Stap_Strp_tox_C MHC_II_alphaStructures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the MHC_II_beta domain has been found. There are 123 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence