2lcw

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[[Image:2lcw.jpg|left|200px]]
 
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==solution structure of FUS/TLS RRM domain==
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The line below this paragraph, containing "STRUCTURE_2lcw", creates the "Structure Box" on the page.
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<StructureSection load='2lcw' size='340' side='right'caption='[[2lcw]]' scene=''>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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== Structural highlights ==
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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<table><tr><td colspan='2'>[[2lcw]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LCW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LCW FirstGlance]. <br>
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or leave the SCENE parameter empty for the default display.
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2lcw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lcw OCA], [https://pdbe.org/2lcw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lcw RCSB], [https://www.ebi.ac.uk/pdbsum/2lcw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lcw ProSAT]</span></td></tr>
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{{STRUCTURE_2lcw| PDB=2lcw | SCENE= }}
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</table>
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== Disease ==
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===solution structure of FUS/TLS RRM domain===
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[https://www.uniprot.org/uniprot/FUS_HUMAN FUS_HUMAN] Frontotemporal dementia with motor neuron disease;Hereditary essential tremor;Amyotrophic lateral sclerosis;Juvenile amyotrophic lateral sclerosis;Myxofibrosarcoma;Myxoid/round cell liposarcoma. A chromosomal aberration involving FUS is found in a patient with malignant myxoid liposarcoma. Translocation t(12;16)(q13;p11) with DDIT3. A chromosomal aberration involving FUS is a cause of acute myeloid leukemia (AML). Translocation t(16;21)(p11;q22) with ERG. The disease may be caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving FUS is found in a patient with angiomatoid fibrous histiocytoma. Translocation t(12;16)(q13;p11.2) with ATF1 generates a chimeric FUS/ATF1 protein. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
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== Function ==
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[https://www.uniprot.org/uniprot/FUS_HUMAN FUS_HUMAN] Binds both single-stranded and double-stranded DNA and promotes ATP-independent annealing of complementary single-stranded DNAs and D-loop formation in superhelical double-stranded DNA. May play a role in maintenance of genomic integrity.
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==About this Structure==
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__TOC__
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[[2lcw]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LCW OCA].
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</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Feng, W.]]
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[[Category: Large Structures]]
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[[Category: Gong, W.]]
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[[Category: Feng W]]
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[[Category: Liu, X.]]
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[[Category: Gong W]]
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[[Category: Niu, C.]]
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[[Category: Liu X]]
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[[Category: Ren, J.]]
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[[Category: Niu C]]
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[[Category: Nucleic acid binding protein]]
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[[Category: Ren J]]
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[[Category: Rna binding protein]]
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[[Category: Rrm]]
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Current revision

solution structure of FUS/TLS RRM domain

PDB ID 2lcw

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OCA

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