Sandbox GGC9

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Early intervention of people with Omenn's syndrome is important, because if left untreated it will be fatal. [4] Treatment of Omenn's syndrome includes bone marrow or cord blood stem cell transplantation. [4]
Early intervention of people with Omenn's syndrome is important, because if left untreated it will be fatal. [4] Treatment of Omenn's syndrome includes bone marrow or cord blood stem cell transplantation. [4]
== Structural highlights ==
== Structural highlights ==
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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.
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The subunit structure is defined as a homodimer.
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The zinc site plays an important role in DNA cleavage; without the zinc site the DNA would not be able to be cleaved and would not form the essential hairpin structure.
<scene name='75/752271/Zinc_ligands/1'>Zinc Ligands</scene>
<scene name='75/752271/Zinc_ligands/1'>Zinc Ligands</scene>

Revision as of 22:06, 22 April 2021

Structure of RAG1/2-DNA Strand Transfer Complex (paired conformation)

Structure of RAG1/2-DNA Strand Transfer Complex (Paired Conformation)

Drag the structure with the mouse to rotate

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.

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