5uzp - Revision history

OCA at 14:30, 6 March 2024

OCA — Wed, 06 Mar 2024 14:30:29 GMT

←Older revision		Revision as of 14:30, 6 March 2024
Line 3:		Line 3:
	<StructureSection load='5uzp' size='340' side='right'caption='[[5uzp]], [[Resolution\|resolution]] 2.29Å' scene=''>		<StructureSection load='5uzp' size='340' side='right'caption='[[5uzp]], [[Resolution\|resolution]] 2.29Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5uzp]] is a 2 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Human Human~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5UZP OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://proteopedia.org/fgij/fg.htm?mol=5UZP FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5uzp]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5UZP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5UZP FirstGlance]. <br>
-	</td></tr><tr id='~~ligand~~'><td class="sblockLbl"><b>[[~~Ligand~~\|~~Ligands~~:]]</b></td><td class="sblockDat" id="~~ligandDat~~">~~<scene name='pdbligand=OAA:OXALOACETATE+ION'>OAA</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]] 2.29Å</td></tr>
-	<tr id='~~gene~~'><td class="sblockLbl"><b>[[~~Gene~~\|~~Gene~~:]]</b></td><td class="sblockDat"~~>CS ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&~~id=~~9606 HUMAN])</td~~><~~/tr>~~	+	<tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=OAA:OXALOACETATE+ION'>OAA</scene></td></tr>
-	~~<tr id~~='~~activity'><td class~~=~~"sblockLbl"><b>Activity~~:~~</b></td><td class="sblockDat"><span class='plainlinks~~'>~~[http://en.wikipedia.org/wiki/Citrate_(Si)-synthase Citrate (Si)-synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.1 2.3.3.1]~~ </~~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=5uzp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5uzp OCA], [https://pdbe.org/5uzp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5uzp RCSB], [https://www.ebi.ac.uk/pdbsum/5uzp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5uzp ProSAT]</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=5uzp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5uzp OCA], [~~http~~://pdbe.org/5uzp PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=5uzp RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/5uzp PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=5uzp ProSAT]</span></td></tr>	+
	</table>		</table>
-	~~<div style~~=~~"background-color:#fffaf0;">~~	+	== Function ==
-	=~~= Publication Abstract from PubMed~~ ==	+	[https://www.uniprot.org/uniprot/CISY_HUMAN CISY_HUMAN]
-	Aspergillus fumigatus is a ubiquitous fungus that is not only a problem in agriculture, but also in healthcare. Aspergillus fumigatus drug resistance is becoming more prominent which is mainly attributed to the widespread use of fungicides in agriculture. The fungi-specific 2-methylcitrate cycle is responsible for detoxifying propionyl-CoA, a toxic metabolite produced as the fungus breaks down proteins and amino acids. The enzyme responsible for this detoxification is 2-methylcitrate synthase (mcsA) and is a potential candidate for the design of new anti-fungals. However, mcsA is very similar in structure to human citrate synthase (hCS) and catalyzes the same reaction. Therefore, both enzymes were studied in parallel to provide foundations for design of mcsA-specific inhibitors. The first crystal structures of citrate synthase from humans and 2-methylcitrate synthase from A. fumigatus are reported. The determined structures capture various conformational states of the enzymes and several inhibitors were identified and characterized. Despite a significant homology, mcsA and hCS display pronounced differences in substrate specificity and cooperativity. Considering that the active sites of the enzymes are almost identical, the differences in reactions catalyzed by enzymes are caused by residues that are in the vicinity of the active site and influence conformational changes of the enzymes.	+
-		+
-	~~Comparative studies of Aspergillus fumigatus 2-methylcitrate synthase and human citrate synthase.,Schlachter CR, Klapper V, Radford T, Chruszcz M Biol Chem. 2019 Nov 26;400(12)~~:~~1567-1581. doi: 10.1515~~/~~hsz-2019-0106. PMID:31141475<ref>PMID:31141475<~~/~~ref>~~	+
-		+
-	~~From MEDLINE®/PubMed®, a database of the U~~.S. ~~National Library of Medicine.<br>~~	+
-	</~~div>~~	+
-	~~<div class="pdbe-citations 5uzp" style="background-color:#fffaf0;"><~~/~~div>~~	+

	==See Also==		==See Also==
	*[[Citrate Synthase 3D structures\|Citrate Synthase 3D structures]]		*[[Citrate Synthase 3D structures\|Citrate Synthase 3D structures]]
-	== References ==
-	<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: Chruszcz, M]]	+	[[Category: Chruszcz M]]
-	[[Category: Schlachter, C]]	+	[[Category: Schlachter C]]
-	~~[[Category: Transferase~~]]	+

OCA at 10:30, 17 June 2020

OCA — Wed, 17 Jun 2020 10:30:24 GMT

←Older revision		Revision as of 10:30, 17 June 2020
Line 1:		Line 1:

	==Crystal structure of citrate synthase mutant A348G from homo sapiens==		==Crystal structure of citrate synthase mutant A348G from homo sapiens==
-	<StructureSection load='5uzp' size='340' side='right' caption='[[5uzp]], [[Resolution\|resolution]] 2.29Å' scene=''>	+	<StructureSection load='5uzp' size='340' side='right'caption='[[5uzp]], [[Resolution\|resolution]] 2.29Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5uzp]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5UZP OCA]. For a <b>guided tour on the structure components</b> use [http://~~oca.weizmann~~.~~ac.il/oca-docs~~/fgij/fg.htm?mol=5UZP FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5uzp]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5UZP OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=5UZP FirstGlance]. <br>
-	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=OAA:OXALOACETATE+ION'>OAA</scene></td></tr>	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=OAA:OXALOACETATE+ION'>OAA</scene></td></tr>
		+	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">CS ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Citrate_(Si)-synthase Citrate (Si)-synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.1 2.3.3.1] </span></td></tr>		<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Citrate_(Si)-synthase Citrate (Si)-synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.1 2.3.3.1] </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=5uzp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5uzp OCA], [http://pdbe.org/5uzp PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5uzp RCSB], [http://www.ebi.ac.uk/pdbsum/5uzp PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5uzp ProSAT]</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=5uzp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5uzp OCA], [http://pdbe.org/5uzp PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5uzp RCSB], [http://www.ebi.ac.uk/pdbsum/5uzp PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5uzp ProSAT]</span></td></tr>
	</table>		</table>
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Aspergillus fumigatus is a ubiquitous fungus that is not only a problem in agriculture, but also in healthcare. Aspergillus fumigatus drug resistance is becoming more prominent which is mainly attributed to the widespread use of fungicides in agriculture. The fungi-specific 2-methylcitrate cycle is responsible for detoxifying propionyl-CoA, a toxic metabolite produced as the fungus breaks down proteins and amino acids. The enzyme responsible for this detoxification is 2-methylcitrate synthase (mcsA) and is a potential candidate for the design of new anti-fungals. However, mcsA is very similar in structure to human citrate synthase (hCS) and catalyzes the same reaction. Therefore, both enzymes were studied in parallel to provide foundations for design of mcsA-specific inhibitors. The first crystal structures of citrate synthase from humans and 2-methylcitrate synthase from A. fumigatus are reported. The determined structures capture various conformational states of the enzymes and several inhibitors were identified and characterized. Despite a significant homology, mcsA and hCS display pronounced differences in substrate specificity and cooperativity. Considering that the active sites of the enzymes are almost identical, the differences in reactions catalyzed by enzymes are caused by residues that are in the vicinity of the active site and influence conformational changes of the enzymes.
		+
		+	Comparative studies of Aspergillus fumigatus 2-methylcitrate synthase and human citrate synthase.,Schlachter CR, Klapper V, Radford T, Chruszcz M Biol Chem. 2019 Nov 26;400(12):1567-1581. doi: 10.1515/hsz-2019-0106. PMID:31141475<ref>PMID:31141475</ref>
		+
		+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>
		+	<div class="pdbe-citations 5uzp" style="background-color:#fffaf0;"></div>
		+
		+	==See Also==
		+	*[[Citrate Synthase 3D structures\|Citrate Synthase 3D structures]]
		+	== References ==
		+	<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Chruszcz, M]]		[[Category: Chruszcz, M]]
	[[Category: Schlachter, C]]		[[Category: Schlachter, C]]
	[[Category: Transferase]]		[[Category: Transferase]]

OCA at 05:00, 8 March 2018

OCA — Thu, 08 Mar 2018 05:00:59 GMT

←Older revision		Revision as of 05:00, 8 March 2018
Line 1:		Line 1:
-	'''Unreleased structure'''

-	~~The entry 5uzp is ON HOLD until Paper Publication~~	+	==Crystal structure of citrate synthase mutant A348G from homo sapiens==
-		+	<StructureSection load='5uzp' size='340' side='right' caption='[[5uzp]], [[Resolution\|resolution]] 2.29Å' scene=''>
-	~~Authors: Schlachter, C., Chruszcz, M.~~	+	== Structural highlights ==
-		+	<table><tr><td colspan='2'>[[5uzp]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5UZP OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5UZP FirstGlance]. <br>
-	~~Description:~~ Crystal structure of citrate synthase mutant A348G from homo sapiens	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=OAA:OXALOACETATE+ION'>OAA</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/Citrate_(Si)-synthase Citrate (Si)-synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.1 2.3.3.1] </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=5uzp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5uzp OCA], [http://pdbe.org/5uzp PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5uzp RCSB], [http://www.ebi.ac.uk/pdbsum/5uzp PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5uzp ProSAT]</span></td></tr>
		+	</table>
		+	__TOC__
		+	</StructureSection>
	[[Category: Chruszcz, M]]		[[Category: Chruszcz, M]]
	[[Category: Schlachter, C]]		[[Category: Schlachter, C]]
		+	[[Category: Transferase]]

OCA at 11:28, 5 April 2017

OCA — Wed, 05 Apr 2017 11:28:00 GMT

←Older revision		Revision as of 11:28, 5 April 2017
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 5uzp is ON HOLD	+	The entry 5uzp is ON HOLD until Paper Publication

	Authors: Schlachter, C., Chruszcz, M.		Authors: Schlachter, C., Chruszcz, M.

OCA: Protected "5uzp" [edit=sysop:move=sysop]

OCA — Thu, 09 Mar 2017 15:08:54 GMT

Protected "5uzp" [edit=sysop:move=sysop]

←Older revision

Revision as of 15:08, 9 March 2017

OCA: New page: '''Unreleased structure''' The entry 5uzp is ON HOLD Authors: Schlachter, C., Chruszcz, M. Description: Crystal structure of citrate synthase mutant A348G from homo sapiens [[Category:...

OCA — Thu, 09 Mar 2017 15:08:53 GMT

New page: '''Unreleased structure''' The entry 5uzp is ON HOLD Authors: Schlachter, C., Chruszcz, M. Description: Crystal structure of citrate synthase mutant A348G from homo sapiens [[Category:...

New page

'''Unreleased structure'''

The entry 5uzp is ON HOLD

Authors: Schlachter, C., Chruszcz, M.

Description: Crystal structure of citrate synthase mutant A348G from homo sapiens
[[Category: Unreleased Structures]]
[[Category: Chruszcz, M]]
[[Category: Schlachter, C]]