5rd4

<StructureSection load='5rd4' size='340' side='right'caption='[[5rd4]], [[Resolution|resolution]] 1.18&Aring;' scene=''>

<table><tr><td colspan='2'>[[5rd4]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Cryphonectria_parasitica Cryphonectria parasitica]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5RD4 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=5RD4 FirstGlance]. <br>

</td></tr><tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Endothiapepsin Endothiapepsin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.22 3.4.23.22] </span></td></tr>

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=5rd4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5rd4 OCA], [http://pdbe.org/5rd4 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5rd4 RCSB], [http://www.ebi.ac.uk/pdbsum/5rd4 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5rd4 ProSAT]</span></td></tr>

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== Publication Abstract from PubMed ==

Crystallographic fragment screening (CFS) provides excellent starting points for projects concerned with drug discovery or biochemical tool compound development. One of the fundamental prerequisites for effective CFS is the availability of a versatile fragment library. Here, we report on the assembly of the 1,103-compound F2X-Universal Library and its 96-compound sub-selection, the F2X-Entry Screen. Both represent the available fragment chemistry and are highly diverse in terms of their 3D-pharmacophore variations. Validation of the F2X-Entry Screen in CFS campaigns using endothiapepsin and the Aar2/RNaseH complex yielded hit rates of 30% and 21%, respectively, and revealed versatile binding sites. Dry presentation of the libraries allows CFS campaigns to be carried out with or without the co-solvent DMSO present. Most of the hits in our validation campaigns could be reproduced also in the absence of DMSO. Consequently, CFS can be carried out more efficiently and for a wider range of conditions and targets.

 

== References ==

[[Category: Cryphonectria parasitica]]

[[Category: Endothiapepsin]]

[[Category: Barthel, T]]

[[Category: Heine, A]]

[[Category: Klebe, G]]

[[Category: Lima, G M.A]]

[[Category: Metz, A]]

[[Category: Mueller, U]]

[[Category: Weiss, M S]]

[[Category: Wollenhaupt, J]]

[[Category: Inhibition]]