6bzm

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'''Unreleased structure'''
 
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The entry 6bzm is ON HOLD until Paper Publication
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==GFGNFGTS from low-complexity/FG repeat domain of Nup98, residues 116-123==
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<StructureSection load='6bzm' size='340' side='right'caption='[[6bzm]], [[Resolution|resolution]] 0.90&Aring;' scene=''>
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Authors: Hughes, M.P., Rodriguez, J.A., Sawaya, M.R., Cascio, D., Chong, L., Gonen, T., Eisenberg, D.S.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6bzm]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6BZM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6BZM FirstGlance]. <br>
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Description: GFGNFGTS from low-complexity/FG repeat domain of Nup98, residues 116-123
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron crystallography, [[Resolution|Resolution]] 0.9&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=6bzm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6bzm OCA], [https://pdbe.org/6bzm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6bzm RCSB], [https://www.ebi.ac.uk/pdbsum/6bzm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6bzm ProSAT]</span></td></tr>
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[[Category: Gonen, T]]
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</table>
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[[Category: Chong, L]]
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== Disease ==
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[[Category: Rodriguez, J.A]]
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[https://www.uniprot.org/uniprot/NUP98_HUMAN NUP98_HUMAN] Note=A chromosomal aberration involving NUP98 is found in a form of acute myeloid leukemia. Translocation t(7;11)(p15;p15) with HOXA9. Translocation t(11;17)(p15;p13) with PHF23. Note=A chromosomal aberration involving NUP98 is found in childhood acute myeloid leukemia. Translocation t(5;11)(q35;p15.5) with NSD1. Translocation t(8;11)(p11.2;p15) with WHSC1L1. Note=A chromosomal aberration involving NUP98 is found in a form of therapy-related myelodysplastic syndrome. Translocation t(11;20)(p15;q11) with TOP1. Note=A chromosomal aberration involving NUP98 is found in a form of T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(3;11)(q12.2;p15.4) with LNP1. Note=A chromosomal aberration involving NUP98 is associated with pediatric acute myeloid leukemia (AML) with intermediate characteristics between M2-M3 French-American-British (FAB) subtypes. Translocation t(9;11)(p22;p15) with PSIP1/LEDGF. The chimeric transcript is an in-frame fusion of NUP98 exon 8 to PSIP1/LEDGF exon 4.
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[[Category: Eisenberg, D.S]]
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== Function ==
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[[Category: Cascio, D]]
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[https://www.uniprot.org/uniprot/NUP98_HUMAN NUP98_HUMAN] Nup98 and Nup96 play a role in the bidirectional transport across the nucleoporin complex (NPC). The FG repeat domains in Nup98 have a direct role in the transport.
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[[Category: Sawaya, M.R]]
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__TOC__
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[[Category: Hughes, M.P]]
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Cascio D]]
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[[Category: Chong L]]
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[[Category: Eisenberg DS]]
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[[Category: Gonen T]]
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[[Category: Hughes MP]]
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[[Category: Rodriguez JA]]
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[[Category: Sawaya MR]]

Current revision

GFGNFGTS from low-complexity/FG repeat domain of Nup98, residues 116-123

PDB ID 6bzm

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