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 </table>
 == Function ==
-[https://www.uniprot.org/uniprot/HB2A_MOUSE HB2A_MOUSE]
+[https://www.uniprot.org/uniprot/HA2B_MOUSE HA2B_MOUSE]
+<div style="background-color:#fffaf0;">
+== Publication Abstract from PubMed ==
+A limited set of T cell receptor (TCR) variable (V) gene segments are used to create a repertoire of TCRs that recognize all major histocompatibility complex (MHC) ligands within a species. How individual alphabetaTCRs are constructed to specifically recognize a limited set of MHC ligands is unclear. Here we have identified a role for the differential pairing of particular V gene segments in creating TCRs that recognized MHC class II ligands exclusively, or cross-reacted with classical and nonclassical MHC class I ligands. Biophysical and structural experiments indicated that TCR specificity for MHC ligands is not driven by germline-encoded pairwise interactions. Rather, identical TCRbeta chains can have altered peptide-MHC (pMHC) binding modes when paired with different TCRalpha chains. The ability of TCR chain pairing to modify how V region residues interact with pMHC helps to explain how the same V genes are used to create TCRs specific for unique MHC ligands.
+A Role for Differential Variable Gene Pairing in Creating T Cell Receptors Specific for Unique Major Histocompatibility Ligands.,Stadinski BD, Trenh P, Smith RL, Bautista B, Huseby PG, Li G, Stern LJ, Huseby ES Immunity. 2011 Nov 16. PMID:22101158<ref>PMID:22101158</ref>
+From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
+</div>
+<div class="pdbe-citations 3rdt" style="background-color:#fffaf0;"></div>
 ==See Also==
 *[[MHC 3D structures|MHC 3D structures]]
 *[[MHC II 3D structures|MHC II 3D structures]]
+== References ==
+<references/>
 __TOC__
 </StructureSection>