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| ==STRUCTURE OF the RAD14 DNA-binding domain IN COMPLEX WITH N2-acetylaminonaphtyl- GUANINE CONTAINING DNA== | | ==STRUCTURE OF the RAD14 DNA-binding domain IN COMPLEX WITH N2-acetylaminonaphtyl- GUANINE CONTAINING DNA== |
- | <StructureSection load='5lcm' size='340' side='right' caption='[[5lcm]], [[Resolution|resolution]] 1.90Å' scene=''> | + | <StructureSection load='5lcm' size='340' side='right'caption='[[5lcm]], [[Resolution|resolution]] 1.90Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[5lcm]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Baker's_yeast Baker's yeast]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LCM OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5LCM FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[5lcm]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae] and [https://en.wikipedia.org/wiki/Saccharomyces_cerevisiae_S288C Saccharomyces cerevisiae S288C]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LCM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5LCM FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9Å</td></tr> |
- | <tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=6TW:[(2~{R},3~{S},5~{R})-5-[2-[(3-ACETAMIDONAPHTHALEN-2-YL)AMINO]-6-OXIDANYLIDENE-1~{H}-PURIN-9-YL]-3-OXIDANYL-OXOLAN-2-YL]METHYL+DIHYDROGEN+PHOSPHITE'>6TW</scene></td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=6TW:[(2~{R},3~{S},5~{R})-5-[2-[(3-ACETAMIDONAPHTHALEN-2-YL)AMINO]-6-OXIDANYLIDENE-1~{H}-PURIN-9-YL]-3-OXIDANYL-OXOLAN-2-YL]METHYL+DIHYDROGEN+PHOSPHITE'>6TW</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">RAD14, YMR201C, YM8325.02C ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=559292 Baker's yeast])</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=5lcm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lcm OCA], [https://pdbe.org/5lcm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5lcm RCSB], [https://www.ebi.ac.uk/pdbsum/5lcm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5lcm ProSAT]</span></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5lcm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lcm OCA], [http://pdbe.org/5lcm PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5lcm RCSB], [http://www.ebi.ac.uk/pdbsum/5lcm PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5lcm ProSAT]</span></td></tr> | + | |
| </table> | | </table> |
| == Function == | | == Function == |
- | [[http://www.uniprot.org/uniprot/RAD14_YEAST RAD14_YEAST]] Involved in nucleotide excision repair. Binds specifically to damaged DNA. Required for the incision step. | + | [https://www.uniprot.org/uniprot/RAD14_YEAST RAD14_YEAST] Involved in nucleotide excision repair. Binds specifically to damaged DNA. Required for the incision step. |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Baker's yeast]] | + | [[Category: Large Structures]] |
- | [[Category: Carell, T]] | + | [[Category: Saccharomyces cerevisiae]] |
- | [[Category: Ebert, C]] | + | [[Category: Saccharomyces cerevisiae S288C]] |
- | [[Category: Schneider, S]] | + | [[Category: Carell T]] |
- | [[Category: Simon, N]] | + | [[Category: Ebert C]] |
- | [[Category: Dna binding protein]] | + | [[Category: Schneider S]] |
- | [[Category: Nucleotide excision repair dna damage recognition]] | + | [[Category: Simon N]] |
| Structural highlights
Function
RAD14_YEAST Involved in nucleotide excision repair. Binds specifically to damaged DNA. Required for the incision step.
Publication Abstract from PubMed
Aromatic amines are strongly carcinogenic compounds. They are activated in the liver to give reactive nitrenium ions that are known to react with the nucleobases within the DNA duplex. The reaction occurs predominantly at the C8-position of the dG base, which gives C8-acetyl-aryl-, or C8-aryl-dG adducts in an electrophilic aromatic substitution reaction. Alternatively, reaction with the exocyclic 2-NH(2) group is observed. While the C8-adducts retain the base pairing properties, base pairing is strongly compromised in the case of the N(2)-adducts. Here we show crystal structures of two DNA lesions, N(2)-acetylnaphthyl-dG and C8-fluorenyl-dG within a DNA duplex recognized by the repair protein Rad14. The structures confirm that two molecules of the repair protein recognize the lesion by induction of a 72 degrees or 78 degrees kink at the site of the lesion. Importantly, the same overall kinked structure is induced by binding of the repair proteins although the lesions differ structurally, resulting in distinct stacking interactions of the lesions within the duplex. The result suggests that the repair protein XPA/Rad14 is a sensor that recognizes flexibility. The protein converts the information that structurally different lesions are present in the duplex into a unifying sharply kinked recognition motif.
Structural insights into the recognition of N(2)-aryl- and C8-aryl DNA lesions by the repair protein XPA/Rad14.,Ebert C, Simon N, Schneider S, Carell T Chembiochem. 2017 Apr 26. doi: 10.1002/cbic.201700169. PMID:28444956[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Ebert C, Simon N, Schneider S, Carell T. Structural insights into the recognition of N(2)-aryl- and C8-aryl DNA lesions by the repair protein XPA/Rad14. Chembiochem. 2017 Apr 26. doi: 10.1002/cbic.201700169. PMID:28444956 doi:http://dx.doi.org/10.1002/cbic.201700169
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