1yls

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|PDB= 1yls |SIZE=350|CAPTION= <scene name='initialview01'>1yls</scene>, resolution 3.00&Aring;
|PDB= 1yls |SIZE=350|CAPTION= <scene name='initialview01'>1yls</scene>, resolution 3.00&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene> and <scene name='pdbligand=DAI:(3AS,9AS)-2-PENTYL-4-HYDROXYMETHYL-3A,4,9,9A-TETRAHYDRO-4,9[1&#39;,2&#39;]-BENZENO-1H-BENZ[F]ISOINDOLE-1,3(2H)-DIONE'>DAI</scene>
+
|LIGAND= <scene name='pdbligand=A:ADENOSINE-5&#39;-MONOPHOSPHATE'>A</scene>, <scene name='pdbligand=C:CYTIDINE-5&#39;-MONOPHOSPHATE'>C</scene>, <scene name='pdbligand=CSL:(D)-2&#39;-METHYLSELENYL-2&#39;-DEOXYCYTIDINE-5&#39;-PHOSPHATE'>CSL</scene>, <scene name='pdbligand=DAI:(3AS,9AS)-2-PENTYL-4-HYDROXYMETHYL-3A,4,9,9A-TETRAHYDRO-4,9[1&#39;,2&#39;]-BENZENO-1H-BENZ[F]ISOINDOLE-1,3(2H)-DIONE'>DAI</scene>, <scene name='pdbligand=G:GUANOSINE-5&#39;-MONOPHOSPHATE'>G</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=U:URIDINE-5&#39;-MONOPHOSPHATE'>U</scene>, <scene name='pdbligand=UMS:2&#39;-METHYLSELENYL-2&#39;-DEOXYURIDINE-5&#39;-PHOSPHATE'>UMS</scene>
|ACTIVITY=
|ACTIVITY=
|GENE=
|GENE=
 +
|DOMAIN=
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|RELATEDENTRY=[[1ykq|1YKQ]], [[1ykv|1YKV]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1yls FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1yls OCA], [http://www.ebi.ac.uk/pdbsum/1yls PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1yls RCSB]</span>
}}
}}
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[[Category: Tereshko, V.]]
[[Category: Tereshko, V.]]
[[Category: Wombacher, R.]]
[[Category: Wombacher, R.]]
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[[Category: DAI]]
 
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[[Category: MG]]
 
[[Category: carbon-carbon bond formation]]
[[Category: carbon-carbon bond formation]]
[[Category: catalytic mechanism]]
[[Category: catalytic mechanism]]
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[[Category: ribozyme]]
[[Category: ribozyme]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 23 14:22:12 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 01:12:18 2008''

Revision as of 22:12, 30 March 2008


PDB ID 1yls

Drag the structure with the mouse to rotate
, resolution 3.00Å
Ligands: , , , , , , ,
Related: 1YKQ, 1YKV


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Crystal structure of selenium-modified Diels-Alder ribozyme complexed with the product of the reaction between N-pentylmaleimide and covalently attached 9-hydroxymethylanthracene


Overview

The majority of structural efforts addressing RNA's catalytic function have focused on natural ribozymes, which catalyze phosphodiester transfer reactions. By contrast, little is known about how RNA catalyzes other types of chemical reactions. We report here the crystal structures of a ribozyme that catalyzes enantioselective carbon-carbon bond formation by the Diels-Alder reaction in the unbound state and in complex with a reaction product. The RNA adopts a lambda-shaped nested pseudoknot architecture whose preformed hydrophobic pocket is precisely complementary in shape to the reaction product. RNA folding and product binding are dictated by extensive stacking and hydrogen bonding, whereas stereoselection is governed by the shape of the catalytic pocket. Catalysis is apparently achieved by a combination of proximity, complementarity and electronic effects. We observe structural parallels in the independently evolved catalytic pocket architectures for ribozyme- and antibody-catalyzed Diels-Alder carbon-carbon bond-forming reactions.

About this Structure

1YLS is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Structural basis for Diels-Alder ribozyme-catalyzed carbon-carbon bond formation., Serganov A, Keiper S, Malinina L, Tereshko V, Skripkin E, Hobartner C, Polonskaia A, Phan AT, Wombacher R, Micura R, Dauter Z, Jaschke A, Patel DJ, Nat Struct Mol Biol. 2005 Mar;12(3):218-24. Epub 2005 Feb 20. PMID:15723077

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