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8s92
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 8s92 is ON HOLD Authors: Li, C., Gao, Y. Description: Structure of N-terminal domains of Walker B mutated MCM8/9 heterohexamer complex with ADP [[C...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Structure of N-terminal domains of Walker B mutated MCM8/9 heterohexamer complex with ADP== | |
| - | + | <StructureSection load='8s92' size='340' side='right'caption='[[8s92]], [[Resolution|resolution]] 4.06Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8s92]] is a 6 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=8S92 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8S92 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]] 4.06Å</td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8s92 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8s92 OCA], [https://pdbe.org/8s92 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8s92 RCSB], [https://www.ebi.ac.uk/pdbsum/8s92 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8s92 ProSAT]</span></td></tr> |
| - | [[Category: Gao | + | </table> |
| - | [[Category: Li | + | == Disease == |
| + | [https://www.uniprot.org/uniprot/MCM8_HUMAN MCM8_HUMAN] NON RARE IN EUROPE: Primary ovarian failure. The disease is caused by mutations affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/MCM8_HUMAN MCM8_HUMAN] Component of the MCM8-MCM9 complex, a complex involved in the repair of double-stranded DNA breaks (DBSs) and DNA interstrand cross-links (ICLs) by homologous recombination (HR) (PubMed:23401855). Required for DNA resection by the MRE11-RAD50-NBN/NBS1 (MRN) complex by recruiting the MRN complex to the repair site and by promoting the complex nuclease activity (PubMed:26215093). Probably by regulating the localization of the MNR complex, indirectly regulates the recruitment of downstream effector RAD51 to DNA damage sites including DBSs and ICLs (PubMed:23401855). The MCM8-MCM9 complex is dispensable for DNA replication and S phase progression (PubMed:23401855). However, may play a non-essential for DNA replication: may be involved in the activation of the prereplicative complex (pre-RC) during G(1) phase by recruiting CDC6 to the origin recognition complex (ORC) (PubMed:15684404). Probably by regulating HR, plays a key role during gametogenesis (By similarity). Stabilizes MCM9 protein (PubMed:23401855, PubMed:26215093).[UniProtKB:Q9CWV1]<ref>PMID:15684404</ref> <ref>PMID:23401855</ref> <ref>PMID:26215093</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Gao Y]] | ||
| + | [[Category: Li C]] | ||
Current revision
Structure of N-terminal domains of Walker B mutated MCM8/9 heterohexamer complex with ADP
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