2jff: Difference between revisions
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<StructureSection load='2jff' size='340' side='right'caption='[[2jff]], [[Resolution|resolution]] 1.89Å' scene=''> | <StructureSection load='2jff' size='340' side='right'caption='[[2jff]], [[Resolution|resolution]] 1.89Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2jff]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[2jff]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2JFF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2JFF FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.89Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=KCX:LYSINE+NZ-CARBOXYLIC+ACID'>KCX</scene>, <scene name='pdbligand=LK2:N-[(6-BUTOXYNAPHTHALEN-2-YL)SULFONYL]-D-GLUTAMIC+ACID'>LK2</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></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=2jff FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2jff OCA], [https://pdbe.org/2jff PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2jff RCSB], [https://www.ebi.ac.uk/pdbsum/2jff PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2jff ProSAT]</span></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=2jff FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2jff OCA], [https://pdbe.org/2jff PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2jff RCSB], [https://www.ebi.ac.uk/pdbsum/2jff PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2jff ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Function == | |||
[https://www.uniprot.org/uniprot/MURD_ECOLI MURD_ECOLI] Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA).[HAMAP-Rule:MF_00639] | |||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Escherichia coli]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Blanot D]] | |||
[[Category: Blanot | [[Category: Contreras-Martel C]] | ||
[[Category: Contreras-Martel | [[Category: Dessen A]] | ||
[[Category: Dessen | [[Category: Gobec S]] | ||
[[Category: Gobec | [[Category: Herve M]] | ||
[[Category: Herve | [[Category: Humljan J]] | ||
[[Category: Humljan | [[Category: Kotnik M]] | ||
[[Category: Kotnik | [[Category: Kristan K]] | ||
[[Category: Kristan | [[Category: Oblak M]] | ||
[[Category: Oblak | [[Category: Solmajer T]] | ||
[[Category: Solmajer | [[Category: Urleb U]] | ||
[[Category: Urleb | |||
Latest revision as of 17:46, 13 December 2023
Crystal structure of MurD ligase in complex with D-Glu containing sulfonamide inhibitorCrystal structure of MurD ligase in complex with D-Glu containing sulfonamide inhibitor
Structural highlights
FunctionMURD_ECOLI Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA).[HAMAP-Rule:MF_00639] Evolutionary Conservation Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. Publication Abstract from PubMedMur ligases play an essential role in the intracellular biosynthesis of bacterial peptidoglycan, the main component of the bacterial cell wall, and represent attractive targets for the design of novel antibacterials. UDP-N-acetylmuramoyl-L-alanine:D-glutamate ligase (MurD) catalyses the addition of D-glutamic acid to the cytoplasmic intermediate UDP-N-acetylmuramoyl-L-alanine (UMA) and is the second in the series of Mur ligases. MurD ligase is highly stereospecific for its substrate, D-glutamic acid (D-Glu). Here, we report the high resolution crystal structures of MurD in complexes with two novel inhibitors designed to mimic the transition state of the reaction, which contain either the D-Glu or the L-Glu moiety. The binding modes of N-sulfonyl-D-Glu and N-sulfonyl-L-Glu derivatives were also characterised kinetically. The results of this study represent an excellent starting point for further development of novel inhibitors of this enzyme. Structural and functional characterization of enantiomeric glutamic acid derivatives as potential transition state analogue inhibitors of MurD ligase.,Kotnik M, Humljan J, Contreras-Martel C, Oblak M, Kristan K, Herve M, Blanot D, Urleb U, Gobec S, Dessen A, Solmajer T J Mol Biol. 2007 Jun 29;370(1):107-15. Epub 2007 May 4. PMID:17507028[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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