4nn3

<StructureSection load='4nn3' size='340' side='right' caption='[[4nn3]], [[Resolution|resolution]] 1.40&Aring;' scene=''>

<table><tr><td colspan='2'>[[4nn3]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Desad Desad]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4NN3 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4NN3 FirstGlance]. <br>

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=ORO:OROTIC+ACID'>ORO</scene>, <scene name='pdbligand=PGE:TRIETHYLENE+GLYCOL'>PGE</scene></td></tr>

<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">Desal_2161 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=526222 DESAD])</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=4nn3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4nn3 OCA], [http://pdbe.org/4nn3 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4nn3 RCSB], [http://www.ebi.ac.uk/pdbsum/4nn3 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4nn3 ProSAT]</span></td></tr>

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== Publication Abstract from PubMed ==

The rate at which genome sequencing data is accruing demands enhanced methods for functional annotation and metabolism discovery. Solute binding proteins (SBPs) facilitate the transport of the first reactant in a metabolic pathway, thereby constraining the regions of chemical space and the chemistries that must be considered for pathway reconstruction. We describe high-throughput protein production and differential scanning fluorimetry platforms, which enabled the screening of 158 SBPs against a 189 component library specifically tailored for this class of proteins. Like all screening efforts, this approach is limited by the practical constraints imposed by construction of the library, i.e., we can study only those metabolites that are known to exist and which can be made in sufficient quantities for experimentation. To move beyond these inherent limitations, we illustrate the promise of crystallographic- and mass spectrometric-based approaches for the unbiased use of entire metabolomes as screening libraries. Together, our approaches identified 40 new SBP ligands, generated experiment-based annotations for 2084 SBPs in 71 isofunctional clusters, and defined numerous metabolic pathways, including novel catabolic pathways for the utilization of ethanolamine as sole nitrogen source and the use of d-Ala-d-Ala as sole carbon source. These efforts begin to define an integrated strategy for realizing the full value of amassing genome sequence data.

 

== References ==

[[Category: Desad]]

[[Category: Almo, S C]]

[[Category: Attonito, J D]]

[[Category: Chowdhury, S]]

[[Category: EFI, Enzyme Function Initiative]]

[[Category: Evans, B]]

[[Category: Gerlt, J A]]

[[Category: Glenn, A Scott]]

[[Category: Hillerich, B]]

[[Category: Imker, H J]]

[[Category: Love, J]]

[[Category: Morisco, L L]]

[[Category: Obaidi, N F.Al]]

[[Category: Seidel, R D]]

[[Category: Sojitra, S]]

[[Category: Stead, M]]

[[Category: Vetting, M W]]

[[Category: Wasserman, S R]]

[[Category: Trap periplasmic solute binding family]]