6n6v - Revision history

OCA at 06:47, 11 October 2023

OCA — Wed, 11 Oct 2023 06:47:09 GMT

←Older revision		Revision as of 06:47, 11 October 2023
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	==OXA-23 mutant F110A/M221A low pH form meropenem complex==		==OXA-23 mutant F110A/M221A low pH form meropenem complex==
-	<StructureSection load='6n6v' size='340' side='right' caption='[[6n6v]], [[Resolution\|resolution]] 1.55Å' scene=''>	+	<StructureSection load='6n6v' size='340' side='right'caption='[[6n6v]], [[Resolution\|resolution]] 1.55Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[6n6v]] is a 1 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Aciba Aciba~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N6V OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=6N6V FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[6n6v]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Acinetobacter_baumannii Acinetobacter baumannii]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6N6V FirstGlance]. <br>
-	</td></tr><tr id='~~ligand~~'><td class="sblockLbl"><b>[[~~Ligand~~\|~~Ligands~~:]]</b></td><td class="sblockDat"~~><scene name='pdbligand=KE1:meropenem,+bound+form'>KE1</scene></td></tr>~~	+	</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models\|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution\|Resolution]] 1.55Å</td></tr>
-	~~<tr~~ id~~='gene'><td class~~="~~sblockLbl~~">~~<b>~~[[~~Gene~~\|~~Gene:~~]]~~</b></td><td class="sblockDat">ari-~~1, bla(OXA-23), bla-OXA-23, bla-oxa-23, bla_1, bla_2, bla_3, blaOXA, blaOXA-23, blaOXA23, OXA-23, oxa-23, oxa23, A7M90_19440, AB719_18095, ABUW_0563, AZE33_05050, AZE33_05100, AZE33_05150, AZE33_05250, C7G90_19950, CAS83_19595, CBE85_20255, CBI29_04474, CEJ63_03230, DV997_16620, DVA79_19285, IX87_16825, IX87_21860, LV38_03424, NG19_0098, SAMEA104305208_04008, SAMEA104305229_06308, SAMEA104305235_03908, SAMEA104305242_04084, SAMEA104305268_03570, SAMEA104305271_04290, SAMEA104305299_06196, SAMEA104305318_04148, SAMEA104305320_04271, SAMEA104305325_04185, SAMEA104305341_03854, SAMEA104305343_03919, SAMEA104305351_03822, SAMEA104305385_00775 ([http://www.~~ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info~~&~~srchmode=5&id=470 ACIBA])~~</td></tr>	+	<tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=KE1:meropenem,+bound+form'>KE1</scene></td></tr>
-	<tr id='~~activity~~'><td class="sblockLbl"><b>~~Activity~~:</b></td><td class="sblockDat"><~~span class~~='~~plainlinks~~'>~~[http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6]~~ </~~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=6n6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n6v OCA], [https://pdbe.org/6n6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6n6v RCSB], [https://www.ebi.ac.uk/pdbsum/6n6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6n6v ProSAT]</span></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=6n6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n6v OCA], [~~http~~://pdbe.org/6n6v PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=6n6v RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/6n6v PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=6n6v ProSAT]</span></td></tr>	+
	</table>		</table>
		+	== Function ==
		+	[https://www.uniprot.org/uniprot/Q9L4P2_ACIBA Q9L4P2_ACIBA]
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 18:		Line 19:
	</div>		</div>
	<div class="pdbe-citations 6n6v" style="background-color:#fffaf0;"></div>		<div class="pdbe-citations 6n6v" style="background-color:#fffaf0;"></div>
		+
		+	==See Also==
		+	*[[Beta-lactamase 3D structures\|Beta-lactamase 3D structures]]
	== References ==		== References ==
	<references/>		<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Aciba~~]]	+	[[Category: Acinetobacter baumannii]]
-	[[Category: ~~Beta-lactamase~~]]	+	[[Category: Large Structures]]
-	[[Category: Smith~~, C A~~]]	+	[[Category: Smith CA]]
-	[[Category: Vakulenko~~, S B]]~~	+	[[Category: Vakulenko SB]]
-	~~[[Category: Antibiotic resistance]]~~	+
-	~~[[Category: Carbapenemase]]~~	+
-	~~[[Category: Hydrolase]]~~	+
-	~~[[Category: Mutant~~]]	+

OCA at 08:48, 26 December 2018

OCA — Wed, 26 Dec 2018 08:48:07 GMT

←Older revision		Revision as of 08:48, 26 December 2018
Line 3:		Line 3:
	<StructureSection load='6n6v' size='340' side='right' caption='[[6n6v]], [[Resolution\|resolution]] 1.55Å' scene=''>		<StructureSection load='6n6v' size='340' side='right' caption='[[6n6v]], [[Resolution\|resolution]] 1.55Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[6n6v]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N6V OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6N6V FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[6n6v]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Aciba Aciba]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N6V OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6N6V FirstGlance]. <br>
	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=KE1:meropenem,+bound+form'>KE1</scene></td></tr>		</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=KE1:meropenem,+bound+form'>KE1</scene></td></tr>
		+	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">ari-1, bla(OXA-23), bla-OXA-23, bla-oxa-23, bla_1, bla_2, bla_3, blaOXA, blaOXA-23, blaOXA23, OXA-23, oxa-23, oxa23, A7M90_19440, AB719_18095, ABUW_0563, AZE33_05050, AZE33_05100, AZE33_05150, AZE33_05250, C7G90_19950, CAS83_19595, CBE85_20255, CBI29_04474, CEJ63_03230, DV997_16620, DVA79_19285, IX87_16825, IX87_21860, LV38_03424, NG19_0098, SAMEA104305208_04008, SAMEA104305229_06308, SAMEA104305235_03908, SAMEA104305242_04084, SAMEA104305268_03570, SAMEA104305271_04290, SAMEA104305299_06196, SAMEA104305318_04148, SAMEA104305320_04271, SAMEA104305325_04185, SAMEA104305341_03854, SAMEA104305343_03919, SAMEA104305351_03822, SAMEA104305385_00775 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=470 ACIBA])</td></tr>
	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6] </span></td></tr>		<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6] </span></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=6n6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n6v OCA], [http://pdbe.org/6n6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6n6v RCSB], [http://www.ebi.ac.uk/pdbsum/6n6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6n6v ProSAT]</span></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=6n6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n6v OCA], [http://pdbe.org/6n6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6n6v RCSB], [http://www.ebi.ac.uk/pdbsum/6n6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6n6v ProSAT]</span></td></tr>
	</table>		</table>
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Class D carbapenemases are enzymes of utmost clinical importance due to their ability to confer resistance to the last resort carbapenem antibiotics. We investigated the role of the conserved hydrophobic bridge in the carbapenemase activity of OXA-23, the major carbapenemase of the important pathogen, Acinetobacter baumannii We show that substitution of the bridge residue Phe110 affects resistance to meropenem and doripenem and has little effect on MICs of imipenem. The opposite effect was observed upon substitution of the other bridge residue, Met221. Complete disruption of the bridge by the F110A/M221A substitution resulted in a significant loss of affinity for doripenem and meropenem, and to a lesser extent, for imipenem, which is reflected in the reduced MICs of these antibiotics. In the wild-type OXA-23, the pyrrolidine ring of the meropenem tail forms a hydrophobic interaction with Phe110 of the bridge. Similar interactions would ensue with ring-containing doripenem but not with imipenem, which lacks this ring. Our structural studies showed that this interaction with the meropenem tail is missing in the F110A/M221A mutant. These data explain why disruption of the interaction between the enzyme and the carbapenem substrate impacts the affinity and MICs of meropenem and doripenem to a larger degree than those of imipenem. Our structures also show that the bridge directs the acylated carbapenem into a specific tautomeric conformation. However, it is not this conformation, but rather the stabilizing interaction between the tail of the antibiotic and the hydrophobic bridge that contributes to the carbapenemase activity of class D beta-lactamases.
		+
		+	Role of the Hydrophobic Bridge in the Carbapenemase Activity of Class D beta-Lactamases.,Stewart NK, Smith CA, Antunes NT, Toth M, Vakulenko SB Antimicrob Agents Chemother. 2018 Dec 10. pii: AAC.02191-18. doi:, 10.1128/AAC.02191-18. PMID:30530607<ref>PMID:30530607</ref>
		+
		+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>
		+	<div class="pdbe-citations 6n6v" style="background-color:#fffaf0;"></div>
		+	== References ==
		+	<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Aciba]]
	[[Category: Beta-lactamase]]		[[Category: Beta-lactamase]]
	[[Category: Smith, C A]]		[[Category: Smith, C A]]

OCA at 08:36, 19 December 2018

OCA — Wed, 19 Dec 2018 08:36:29 GMT

←Older revision		Revision as of 08:36, 19 December 2018
Line 1:		Line 1:
-	'''Unreleased structure'''

-	~~The entry~~ 6n6v is ~~ON HOLD~~	+	==OXA-23 mutant F110A/M221A low pH form meropenem complex==
-		+	<StructureSection load='6n6v' size='340' side='right' caption='[[6n6v]], [[Resolution\|resolution]] 1.55Å' scene=''>
-	~~Authors~~: ~~Smith~~, C.A., ~~Vakulenko~~, S.B.	+	== Structural highlights ==
-		+	<table><tr><td colspan='2'>[[6n6v]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6N6V OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6N6V FirstGlance]. <br>
-	~~Description~~: ~~OXA~~-~~23 mutant F110A/M221A low pH form meropenem complex~~	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=KE1:meropenem,+bound+form'>KE1</scene></td></tr>
-	[[Category: ~~Unreleased Structures~~]]	+	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Beta-lactamase Beta-lactamase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.2.6 3.5.2.6] </span></td></tr>
-	[[Category: Vakulenko, S.B]]	+	<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=6n6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6n6v OCA], [http://pdbe.org/6n6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6n6v RCSB], [http://www.ebi.ac.uk/pdbsum/6n6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6n6v ProSAT]</span></td></tr>
-	[[Category: ~~Smith, C.A~~]]	+	</table>
		+	__TOC__
		+	</StructureSection>
		+	[[Category: Beta-lactamase]]
		+	[[Category: Smith, C A]]
		+	[[Category: Vakulenko, S B]]
		+	[[Category: Antibiotic resistance]]
		+	[[Category: Carbapenemase]]
		+	[[Category: Hydrolase]]
		+	[[Category: Mutant]]

OCA: Protected "6n6v" [edit=sysop:move=sysop]

OCA — Wed, 05 Dec 2018 05:17:53 GMT

Protected "6n6v" [edit=sysop:move=sysop]

←Older revision

Revision as of 05:17, 5 December 2018

OCA: New page: '''Unreleased structure''' The entry 6n6v is ON HOLD Authors: Smith, C.A., Vakulenko, S.B. Description: OXA-23 mutant F110A/M221A low pH form meropenem complex [[Category: Unreleased S...

OCA — Wed, 05 Dec 2018 05:17:51 GMT

New page: '''Unreleased structure''' The entry 6n6v is ON HOLD Authors: Smith, C.A., Vakulenko, S.B. Description: OXA-23 mutant F110A/M221A low pH form meropenem complex [[Category: Unreleased S...

New page

'''Unreleased structure'''

The entry 6n6v is ON HOLD

Authors: Smith, C.A., Vakulenko, S.B.

Description: OXA-23 mutant F110A/M221A low pH form meropenem complex
[[Category: Unreleased Structures]]
[[Category: Vakulenko, S.B]]
[[Category: Smith, C.A]]