6n0r
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of Tdp1 catalytic domain in complex with compound XZ572== | |
| - | + | <StructureSection load='6n0r' size='340' side='right'caption='[[6n0r]], [[Resolution|resolution]] 1.54Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6n0r]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N0R OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6N0R FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=K8D:4-(methylamino)benzene-1,2-dicarboxylic+acid'>K8D</scene></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=6n0r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n0r OCA], [http://pdbe.org/6n0r PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6n0r RCSB], [http://www.ebi.ac.uk/pdbsum/6n0r PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6n0r ProSAT]</span></td></tr> |
| - | [[ | + | </table> |
| - | [[ | + | == Disease == |
| - | [[Category: | + | [[http://www.uniprot.org/uniprot/TYDP1_HUMAN TYDP1_HUMAN]] Defects in TDP1 are the cause of spinocerebellar ataxia autosomal recessive with axonal neuropathy (SCAN1) [MIM:[http://omim.org/entry/607250 607250]]. SCAN1 is an autosomal recessive cerebellar ataxia (ARCA) associated with peripheral axonal motor and sensory neuropathy, distal muscular atrophy, pes cavus and steppage gait as seen in Charcot-Marie-Tooth neuropathy. All affected individuals have normal intelligence.<ref>PMID:16141202</ref> <ref>PMID:15647511</ref> <ref>PMID:12244316</ref> <ref>PMID:17948061</ref> <ref>PMID:15920477</ref> |
| - | [[Category: | + | == Function == |
| + | [[http://www.uniprot.org/uniprot/TYDP1_HUMAN TYDP1_HUMAN]] DNA repair enzyme that can remove a variety of covalent adducts from DNA through hydrolysis of a 3'-phosphodiester bond, giving rise to DNA with a free 3' phosphate. Catalyzes the hydrolysis of dead-end complexes between DNA and the topoisomerase I active site tyrosine residue. Hydrolyzes 3'-phosphoglycolates on protruding 3' ends on DNA double-strand breaks due to DNA damage by radiation and free radicals. Acts on blunt-ended double-strand DNA breaks and on single-stranded DNA. Has low 3'exonuclease activity and can remove a single nucleoside from the 3'end of DNA and RNA molecules with 3'hydroxyl groups. Has no exonuclease activity towards DNA or RNA with a 3'phosphate.<ref>PMID:12023295</ref> <ref>PMID:15111055</ref> <ref>PMID:15811850</ref> <ref>PMID:16141202</ref> <ref>PMID:22822062</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Burke, T R]] | ||
[[Category: Kiselev, E]] | [[Category: Kiselev, E]] | ||
| - | [[Category: | + | [[Category: Lountos, G T]] |
| - | + | ||
| - | + | ||
[[Category: Needle, D]] | [[Category: Needle, D]] | ||
| + | [[Category: Pommier, Y]] | ||
| + | [[Category: Tropea, J E]] | ||
| + | [[Category: Waugh, D S]] | ||
| + | [[Category: Zhao, X Z]] | ||
| + | [[Category: Anti-cancer drug design]] | ||
| + | [[Category: Dna binding protein]] | ||
| + | [[Category: Fragment based drug design]] | ||
| + | [[Category: Hydrolase]] | ||
Revision as of 11:04, 13 November 2019
Crystal structure of Tdp1 catalytic domain in complex with compound XZ572
| |||||||||||
