1z00: Difference between revisions
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==Solution structure of the C-terminal domain of ERCC1 complexed with the C-terminal domain of XPF== | ==Solution structure of the C-terminal domain of ERCC1 complexed with the C-terminal domain of XPF== | ||
<StructureSection load='1z00' size='340' side='right'caption='[[1z00 | <StructureSection load='1z00' size='340' side='right'caption='[[1z00]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1z00]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[1z00]] is a 2 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=1Z00 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1Z00 FirstGlance]. <br> | ||
</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=1z00 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1z00 OCA], [https://pdbe.org/1z00 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1z00 RCSB], [https://www.ebi.ac.uk/pdbsum/1z00 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1z00 ProSAT]</span></td></tr> | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=1z00 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1z00 OCA], [https://pdbe.org/1z00 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1z00 RCSB], [https://www.ebi.ac.uk/pdbsum/1z00 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1z00 ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/ERCC1_HUMAN ERCC1_HUMAN] Defects in ERCC1 are the cause of cerebro-oculo-facio-skeletal syndrome type 4 (COFS4) [MIM:[https://omim.org/entry/610758 610758]. COFS is a degenerative autosomal recessive disorder of prenatal onset affecting the brain, eye and spinal cord. After birth, it leads to brain atrophy, hypoplasia of the corpus callosum, hypotonia, cataracts, microcornea, optic atrophy, progressive joint contractures and growth failure. Facial dysmorphism is a constant feature. Abnormalities of the skull, eyes, limbs, heart and kidney also occur.<ref>PMID:17273966</ref> | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/ERCC1_HUMAN ERCC1_HUMAN] Structure-specific DNA repair endonuclease responsible for the 5'-incision during DNA repair. | |||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Ab | [[Category: Ab E]] | ||
[[Category: Boelens | [[Category: Boelens R]] | ||
[[Category: Das | [[Category: Das D]] | ||
[[Category: Folkers | [[Category: Folkers G]] | ||
[[Category: Hoeijmakers | [[Category: Hoeijmakers JHJ]] | ||
[[Category: Jaspers | [[Category: Jaspers NGJ]] | ||
[[Category: Kaptein | [[Category: Kaptein R]] | ||
[[Category: Odijk | [[Category: Odijk H]] | ||
[[Category: Tripsianes | [[Category: Tripsianes K]] | ||
Latest revision as of 08:07, 15 May 2024
Solution structure of the C-terminal domain of ERCC1 complexed with the C-terminal domain of XPF
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