Sandbox GGC9
From Proteopedia
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The subunit structure is defined as a homodimer. The RAG complex consists of RAG1 and RAG2 with associated components of HMGB1 and HMGB2. The complex also interacts with DCAF1 and leads to the recruitment of another protein complex to ubiquitinate proteins. | The subunit structure is defined as a homodimer. The RAG complex consists of RAG1 and RAG2 with associated components of HMGB1 and HMGB2. The complex also interacts with DCAF1 and leads to the recruitment of another protein complex to ubiquitinate proteins. | ||
- | + | <scene name='75/752271/Zinc_ligands/1'>Zinc Ligands</scene> | |
</StructureSection> | </StructureSection> |
Revision as of 21:59, 22 April 2021
Structure of RAG1/2-DNA Strand Transfer Complex (paired conformation)
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References
[1] Grazini U, Zanardi F, Citterio E, Casola S, Goding CR, McBlane F. The RING domain of RAG1 ubiquitylates histone H3: a novel activity in chromatin-mediated regulation of V(D)J joining. Mol Cell. 2010 Jan 29;37(2):282-93. doi: 10.1016/j.molcel.2009.12.035. PMID: 20122409.
[2] Zhang Y, Corbett E, Wu S, Schatz DG. Structural basis for the activation and suppression of transposition during evolution of the RAG recombinase. EMBO J. 2020 Nov 2;39(21):e105857. doi: 10.15252/embj.2020105857. Epub 2020 Sep 18. PMID: 32945578; PMCID: PMC7604617.
[3] Chen, Karin et al. “Autoimmunity due to RAG deficiency and estimated disease incidence in RAG1/2 mutations.” The Journal of allergy and clinical immunology vol. 133,3 (2014): 880-2.e10. doi:10.1016/j.jaci.2013.11.038
[4] Omenn syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. Rarediseases.info.nih.gov. (2021). Retrieved 7 April 2021, from https://rarediseases.info.nih.gov/diseases/8198/omenn-syndrome.