3jbw: Difference between revisions

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'''Unreleased structure'''


The entry 3jbw is ON HOLD
==Cryo-electron microscopy structure of RAG Paired Complex (with NBD, no symmetry)==
<SX load='3jbw' size='340' side='right' viewer='molstar' caption='[[3jbw]], [[Resolution|resolution]] 4.63&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[3jbw]] is a 10 chain structure with sequence from [https://en.wikipedia.org/wiki/Danio_rerio Danio rerio] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3JBW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3JBW FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 4.631&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3jbw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3jbw OCA], [https://pdbe.org/3jbw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3jbw RCSB], [https://www.ebi.ac.uk/pdbsum/3jbw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3jbw ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/RAG2_DANRE RAG2_DANRE] Core component of the RAG complex, a multiprotein complex that mediates the DNA cleavage phase during V(D)J recombination. V(D)J recombination assembles a diverse repertoire of immunoglobulin and T-cell receptor genes in developing B and T lymphocytes through rearrangement of different V (variable), in some cases D (diversity), and J (joining) gene segments. DNA cleavage by the RAG complex occurs in 2 steps: a first nick is introduced in the top strand immediately upstream of the heptamer, generating a 3'-hydroxyl group that can attack the phosphodiester bond on the opposite strand in a direct transesterification reaction, thereby creating 4 DNA ends: 2 hairpin coding ends and 2 blunt, 5'-phosphorylated ends. In the RAG complex, rag2 is not the catalytic component but is required for all known catalytic activities mediated by RAG1. It probably acts as a sensor of chromatin state that recruits the RAG complex to H3K4me3 (By similarity).


Authors: Ru, H., Chambers, M.G., Fu, T.-M., Tong, A.B., Liao, M., Wu, H.
==See Also==
 
*[[Recombination-activating gene|Recombination-activating gene]]
Description: Cryo-electron microscopy structure of RAG Paired Complex (with NBD, no symmetry)
*[[Recombination-activating gene 3D structures|Recombination-activating gene 3D structures]]
[[Category: Unreleased Structures]]
__TOC__
[[Category: Fu, T.-M]]
</SX>
[[Category: Tong, A.B]]
[[Category: Danio rerio]]
[[Category: Ru, H]]
[[Category: Homo sapiens]]
[[Category: Liao, M]]
[[Category: Large Structures]]
[[Category: Chambers, M.G]]
[[Category: Chambers MG]]
[[Category: Wu, H]]
[[Category: Fu T-M]]
[[Category: Liao M]]
[[Category: Ru H]]
[[Category: Tong AB]]
[[Category: Wu H]]

Latest revision as of 08:43, 7 February 2024

Cryo-electron microscopy structure of RAG Paired Complex (with NBD, no symmetry)

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