5a9q
From Proteopedia
(Difference between revisions)
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<SX load='5a9q' size='340' side='right' viewer='molstar' caption='[[5a9q]], [[Resolution|resolution]] 23.00Å' scene=''> | <SX load='5a9q' size='340' side='right' viewer='molstar' caption='[[5a9q]], [[Resolution|resolution]] 23.00Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[5a9q]] is a 38 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[5a9q]] is a 38 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=5A9Q OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5A9Q FirstGlance]. <br> |
- | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | </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=5a9q FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5a9q OCA], [https://pdbe.org/5a9q PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5a9q RCSB], [https://www.ebi.ac.uk/pdbsum/5a9q PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5a9q ProSAT]</span></td></tr> |
</table> | </table> | ||
- | == Disease == | ||
- | [[http://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. [[http://www.uniprot.org/uniprot/NU155_HUMAN NU155_HUMAN]] Familial atrial fibrillation. The disease is caused by mutations affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
- | [ | + | [https://www.uniprot.org/uniprot/NUP43_HUMAN NUP43_HUMAN] Component of the Nup107-160 subcomplex of the nuclear pore complex (NPC). The Nup107-160 subcomplex is required for the assembly of a functional NPC. The Nup107-160 subcomplex is also required for normal kinetochore microtubule attachment, mitotic progression and chromosome segregation.<ref>PMID:17363900</ref> |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Andres-Pons | + | [[Category: Andres-Pons A]] |
- | [[Category: Antonin | + | [[Category: Antonin W]] |
- | + | [[Category: Banterle N]] | |
- | [[Category: Banterle | + | [[Category: Beck M]] |
- | [[Category: Beck | + | [[Category: Bork P]] |
- | [[Category: Bork | + | [[Category: Buczak K]] |
- | [[Category: Buczak | + | [[Category: Bui KH]] |
- | [[Category: Bui | + | [[Category: DiGuilio A]] |
- | [[Category: DiGuilio | + | [[Category: Glavy JS]] |
- | [[Category: Glavy | + | [[Category: Hagen W]] |
- | [[Category: Hagen | + | [[Category: Kastritis P]] |
- | [[Category: Kastritis | + | [[Category: Kosinski J]] |
- | [[Category: Kosinski | + | [[Category: Lemke EA]] |
- | [[Category: Lemke | + | [[Category: Mackmull M]] |
- | [[Category: Mackmull | + | [[Category: Mosalaganti S]] |
- | [[Category: Mosalaganti | + | [[Category: Ori A]] |
- | [[Category: Ori | + | [[Category: Parca L]] |
- | [[Category: Parca | + | [[Category: Sparks L]] |
- | [[Category: Sparks | + | [[Category: Vollmer B]] |
- | [[Category: Vollmer | + | [[Category: Von Appen A]] |
- | [[Category: | + |
Revision as of 04:46, 25 May 2023
Human nuclear pore complex
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Categories: Homo sapiens | Large Structures | Andres-Pons A | Antonin W | Banterle N | Beck M | Bork P | Buczak K | Bui KH | DiGuilio A | Glavy JS | Hagen W | Kastritis P | Kosinski J | Lemke EA | Mackmull M | Mosalaganti S | Ori A | Parca L | Sparks L | Vollmer B | Von Appen A