9b8s: Difference between revisions

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New page: '''Unreleased structure''' The entry 9b8s is ON HOLD Authors: Wang, F., He, Q., Li, H. Description: Human polymerase epsilon bound to PCNA and DNA in the nucleotide exchange state [[Ca...
 
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'''Unreleased structure'''


The entry 9b8s is ON HOLD
==Human polymerase epsilon bound to PCNA and DNA in the nucleotide exchange state==
 
<StructureSection load='9b8s' size='340' side='right'caption='[[9b8s]], [[Resolution|resolution]] 5.01&Aring;' scene=''>
Authors: Wang, F., He, Q., Li, H.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9b8s]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/DNA_molecule DNA molecule] 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=9B8S OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9B8S FirstGlance]. <br>
Description: Human polymerase epsilon bound to PCNA and DNA in the nucleotide exchange state
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 5.01&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9b8s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9b8s OCA], [https://pdbe.org/9b8s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9b8s RCSB], [https://www.ebi.ac.uk/pdbsum/9b8s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9b8s ProSAT]</span></td></tr>
[[Category: Li, H]]
</table>
[[Category: Wang, F]]
== Disease ==
[[Category: He, Q]]
[https://www.uniprot.org/uniprot/DPOE1_HUMAN DPOE1_HUMAN] Facial dysmorphism - immunodeficiency - livedo - short stature. Disease susceptibility is associated with variations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/DPOE1_HUMAN DPOE1_HUMAN] Participates in DNA repair and in chromosomal DNA replication.
__TOC__
</StructureSection>
[[Category: DNA molecule]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: He Q]]
[[Category: Li H]]
[[Category: Wang F]]