9w7p: Difference between revisions

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'''Unreleased structure'''


The entry 9w7p is ON HOLD  until Paper Publication
==Crystal Structure of Ledaborbactam in complex with SME-1 class A Carbapenemase==
<StructureSection load='9w7p' size='340' side='right'caption='[[9w7p]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9w7p]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Serratia_marcescens Serratia marcescens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9W7P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9W7P FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.2&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1MBD:(3~{R})-2-oxidanyl-3-(propanoylamino)-3,4-dihydro-1,2-benzoxaborinine-8-carboxylic+acid'>A1MBD</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</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=9w7p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9w7p OCA], [https://pdbe.org/9w7p PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9w7p RCSB], [https://www.ebi.ac.uk/pdbsum/9w7p PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9w7p ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/BLAS1_SERMA BLAS1_SERMA] Class A beta-lactamase which confers resistance to the beta-lactam antibiotics, including penicillins, some cephalosporins and carbapenems, to JM109 strain E.coli (PubMed:11807251, PubMed:8092824). Acts via hydrolysis of the beta-lactam ring (PubMed:11036019, PubMed:8092824). Has penicillin-, cephalosporin- and carbapenem-hydrolyzing activities (PubMed:11036019).<ref>PMID:11036019</ref> <ref>PMID:11807251</ref> <ref>PMID:8092824</ref>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Bicyclic boronic acids inhibit SME-1 carbapenemase via a unique pi-pi stacking with His105 and covalent interaction with Ser70. Ledaborbactam shows the strongest inhibition, with the lowest k(i) and enhanced structural stability. X-ray crystallography and molecular dynamics reveal key features helpful in structure-based optimization of boronates targeting class A beta-lactamases.


Authors: Dhankhar, K., Hazra, S.
Beyond structure and activity: targeting class A carbapenemases with monocyclic and bicyclic boronic acids to counter antimicrobial resistance.,Dhankhar K, Hazra M, Nair ASR, Alhmeidi Alkhatib AE, Mishra NC, Hazra S Org Biomol Chem. 2025 Nov 11. doi: 10.1039/d5ob01703c. PMID:41217385<ref>PMID:41217385</ref>


Description: Crystal Structure of Ledaborbactam in complex with SME-1 class A Carbapenemase
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Dhankhar, K]]
<div class="pdbe-citations 9w7p" style="background-color:#fffaf0;"></div>
[[Category: Hazra, S]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Serratia marcescens]]
[[Category: Dhankhar K]]
[[Category: Hazra S]]

Latest revision as of 07:55, 19 November 2025

Crystal Structure of Ledaborbactam in complex with SME-1 class A Carbapenemase

9w7p, resolution 2.20Å

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