5lts - Revision history

OCA at 18:49, 18 October 2023

OCA — Wed, 18 Oct 2023 18:49:12 GMT

←Older revision		Revision as of 18:49, 18 October 2023
Line 1:		Line 1:

	==Crystal structure of Lymphocytic choriomeningitis mammarenavirus endonuclease Mutant D118A==		==Crystal structure of Lymphocytic choriomeningitis mammarenavirus endonuclease Mutant D118A==
-	<StructureSection load='5lts' size='340' side='right' caption='[[5lts]], [[Resolution\|resolution]] 2.51Å' scene=''>	+	<StructureSection load='5lts' size='340' side='right'caption='[[5lts]], [[Resolution\|resolution]] 2.51Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5lts]] is a 2 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Lcmv Lcmv~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LTS OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=5LTS FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5lts]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Lymphocytic_choriomeningitis_mammarenavirus Lymphocytic choriomeningitis mammarenavirus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LTS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5LTS 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=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</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]] 2.51Å</td></tr>
-	~~<tr~~ id~~='related'><td class~~="~~sblockLbl~~">~~<b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5ltf\|5ltf]]~~, [[~~5ltn~~\|~~5ltn]], [[5t2t\|5t2t~~]]</td></tr>	+	<tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr>
-	<tr id='~~gene~~'><td class="sblockLbl"><b>[[~~Gene~~\|~~Gene~~:]]</b></td><td class="sblockDat">~~L, KUE_IGS310002 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode~~=~~Info&srchmode~~=~~5&id=11623 LCMV])</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=5lts FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lts OCA], [https://pdbe.org/5lts PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5lts RCSB], [https://www.ebi.ac.uk/pdbsum/5lts PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5lts ProSAT]</span></td></tr>
-	<~~tr id~~='~~activity'><td class~~=~~"sblockLbl"><b>Activity~~:~~</b~~></td><~~td class~~=~~"sblockDat"><span class~~=~~'plainlinks~~'>~~[http://en.wikipedia.org/wiki/RNA-directed_RNA_polymerase RNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.48 2.7.7.48]~~ </~~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=5lts FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lts OCA], [~~http~~://pdbe.org/5lts PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=5lts RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/5lts PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=5lts ProSAT]</span></td></tr>	+
	</table>		</table>
	== Function ==		== Function ==
-	[~~[http~~://www.uniprot.org/uniprot/~~A0A059U382_9VIRU A0A059U382_9VIRU]~~] RNA-dependent RNA polymerase which is responsible for replication and transcription of the viral RNA genome. During transcription, synthesizes 4 subgenomic RNAs, and assures their capping by a cap-snatching mechanism, in which cellular capped pre-mRNA are used to generate primers for viral transcription. The 3'-end of subgenomic mRNAs molecules are heterogeneous and not polyadenylated. The replicase function is to direct synthesis of antigenomic and genomic RNA which are encapsidated and non capped. As a consequence of the use of the same enzyme for both transcription and replication, these mechanisms need to be well coordinated. These processes may be regulated by proteins N and Z in a dose-dependent manner.~~[PIRNR~~:~~PIRNR000836]~~	+	[https://www.uniprot.org/uniprot/L_LYCVA L_LYCVA] RNA-dependent RNA polymerase which is responsible for replication and transcription of the viral RNA genome. During transcription, synthesizes 4 subgenomic RNAs, and assures their capping by a cap-snatching mechanism, in which cellular capped pre-mRNA are used to generate primers for viral transcription. The 3'-end of subgenomic mRNAs molecules are heterogeneous and not polyadenylated. The replicase function is to direct synthesis of antigenomic and genomic RNA which are encapsidated and non capped. As a consequence of the use of the same enzyme for both transcription and replication, these mechanisms need to be well coordinated. These processes may be regulated by proteins N and Z in a dose-dependent manner.<ref>PMID:7682625</ref>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 23:		Line 21:

	==See Also==		==See Also==
-	*[[RNA polymerase\|RNA polymerase]]	+	*[[RNA polymerase 3D structures\|RNA polymerase 3D structures]]
	== References ==		== References ==
	<references/>		<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Lcmv~~]]	+	[[Category: Large Structures]]
-	[[Category: ~~RNA-directed RNA polymerase~~]]	+	[[Category: Lymphocytic choriomeningitis mammarenavirus]]
-	[[Category: Alvarez, K]]	+	[[Category: Alvarez K]]
-	[[Category: Canard, B]]	+	[[Category: Canard B]]
-	[[Category: Ferron, F]]	+	[[Category: Ferron F]]
-	[[Category: Saez-Ayala, M]]	+	[[Category: Saez-Ayala M]]
-	[[Category: Yekwa~~, E L]]~~	+	[[Category: Yekwa EL]]
-	~~[[Category: Endonuclease]]~~	+
-	~~[[Category: Lcmv arenavirus]]~~	+
-	~~[[Category: Transferase~~]]	+

OCA at 05:46, 30 May 2018

OCA — Wed, 30 May 2018 05:46:54 GMT

←Older revision		Revision as of 05:46, 30 May 2018
Line 12:		Line 12:
	== Function ==		== Function ==
	[[http://www.uniprot.org/uniprot/A0A059U382_9VIRU A0A059U382_9VIRU]] RNA-dependent RNA polymerase which is responsible for replication and transcription of the viral RNA genome. During transcription, synthesizes 4 subgenomic RNAs, and assures their capping by a cap-snatching mechanism, in which cellular capped pre-mRNA are used to generate primers for viral transcription. The 3'-end of subgenomic mRNAs molecules are heterogeneous and not polyadenylated. The replicase function is to direct synthesis of antigenomic and genomic RNA which are encapsidated and non capped. As a consequence of the use of the same enzyme for both transcription and replication, these mechanisms need to be well coordinated. These processes may be regulated by proteins N and Z in a dose-dependent manner.[PIRNR:PIRNR000836]		[[http://www.uniprot.org/uniprot/A0A059U382_9VIRU A0A059U382_9VIRU]] RNA-dependent RNA polymerase which is responsible for replication and transcription of the viral RNA genome. During transcription, synthesizes 4 subgenomic RNAs, and assures their capping by a cap-snatching mechanism, in which cellular capped pre-mRNA are used to generate primers for viral transcription. The 3'-end of subgenomic mRNAs molecules are heterogeneous and not polyadenylated. The replicase function is to direct synthesis of antigenomic and genomic RNA which are encapsidated and non capped. As a consequence of the use of the same enzyme for both transcription and replication, these mechanisms need to be well coordinated. These processes may be regulated by proteins N and Z in a dose-dependent manner.[PIRNR:PIRNR000836]
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	The Arenaviridae family, together with the Bunyaviridae and Orthomyxoviridae families, is one of the three negative-stranded RNA viral families that encode an endonuclease in their genome. The endonuclease domain is at the N-terminus of the L protein, a multifunctional protein that includes the RNA-dependent RNA polymerase. The synthesis of mRNA in arenaviruses is a process that is primed by capped nucleotides that are 'stolen' from the cellular mRNA by the endonuclease domain in cooperation with other domains of the L protein. This molecular mechanism has been demonstrated previously for the endonuclease of the prototype Lymphocytic choriomeningitis virus (LCMV). However, the mode of action of this enzyme is not fully understood as the original structure did not contain catalytic metal ions. The pivotal role played by the cap-snatching process in the life cycle of the virus and the highly conserved nature of the endonuclease domain make it a target of choice for the development of novel antiviral therapies. Here, the binding affinities of two diketo-acid (DKA) compounds (DPBA and L-742,001) for the endonuclease domain of LCMV were evaluated using biophysical methods. X-ray structures of the LCMV endonuclease domain with catalytic ions in complex with these two compounds were determined, and their efficacies were assessed in an in vitro endonuclease-activity assay. Based on these data and computational simulation, two new DKAs were synthesized. The LCMV endonuclease domain exhibits a good affinity for these DKAs, making them a good starting point for the design of arenavirus endonuclease inhibitors. In addition to providing the first example of an X-ray structure of an arenavirus endonuclease incorporating a ligand, this study provides a proof of concept that the design of optimized inhibitors against the arenavirus endonuclease is possible.
		+
		+	Crystal structures of Lymphocytic choriomeningitis virus endonuclease domain complexed with diketo-acid ligands.,Saez-Ayala M, Yekwa EL, Carcelli M, Canard B, Alvarez K, Ferron F IUCrJ. 2018 Feb 22;5(Pt 2):223-235. doi: 10.1107/S2052252518001021. eCollection, 2018 Mar 1. PMID:29765612<ref>PMID:29765612</ref>
		+
		+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>
		+	<div class="pdbe-citations 5lts" style="background-color:#fffaf0;"></div>

	==See Also==		==See Also==
	*[[RNA polymerase\|RNA polymerase]]		*[[RNA polymerase\|RNA polymerase]]
		+	== References ==
		+	<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>

OCA at 06:24, 18 April 2018

OCA — Wed, 18 Apr 2018 06:24:49 GMT

←Older revision		Revision as of 06:24, 18 April 2018
Line 3:		Line 3:
	<StructureSection load='5lts' size='340' side='right' caption='[[5lts]], [[Resolution\|resolution]] 2.51Å' scene=''>		<StructureSection load='5lts' size='340' side='right' caption='[[5lts]], [[Resolution\|resolution]] 2.51Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5lts]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LTS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5LTS FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5lts]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Lcmv Lcmv]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LTS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5LTS 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=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr>		</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=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr>
	<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5ltf\|5ltf]], [[5ltn\|5ltn]], [[5t2t\|5t2t]]</td></tr>		<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5ltf\|5ltf]], [[5ltn\|5ltn]], [[5t2t\|5t2t]]</td></tr>
		+	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">L, KUE_IGS310002 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=11623 LCMV])</td></tr>
	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/RNA-directed_RNA_polymerase RNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.48 2.7.7.48] </span></td></tr>		<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/RNA-directed_RNA_polymerase RNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.48 2.7.7.48] </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=5lts FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lts OCA], [http://pdbe.org/5lts PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5lts RCSB], [http://www.ebi.ac.uk/pdbsum/5lts PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5lts 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=5lts FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lts OCA], [http://pdbe.org/5lts PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5lts RCSB], [http://www.ebi.ac.uk/pdbsum/5lts PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5lts ProSAT]</span></td></tr>
Line 11:		Line 12:
	== Function ==		== Function ==
	[[http://www.uniprot.org/uniprot/A0A059U382_9VIRU A0A059U382_9VIRU]] RNA-dependent RNA polymerase which is responsible for replication and transcription of the viral RNA genome. During transcription, synthesizes 4 subgenomic RNAs, and assures their capping by a cap-snatching mechanism, in which cellular capped pre-mRNA are used to generate primers for viral transcription. The 3'-end of subgenomic mRNAs molecules are heterogeneous and not polyadenylated. The replicase function is to direct synthesis of antigenomic and genomic RNA which are encapsidated and non capped. As a consequence of the use of the same enzyme for both transcription and replication, these mechanisms need to be well coordinated. These processes may be regulated by proteins N and Z in a dose-dependent manner.[PIRNR:PIRNR000836]		[[http://www.uniprot.org/uniprot/A0A059U382_9VIRU A0A059U382_9VIRU]] RNA-dependent RNA polymerase which is responsible for replication and transcription of the viral RNA genome. During transcription, synthesizes 4 subgenomic RNAs, and assures their capping by a cap-snatching mechanism, in which cellular capped pre-mRNA are used to generate primers for viral transcription. The 3'-end of subgenomic mRNAs molecules are heterogeneous and not polyadenylated. The replicase function is to direct synthesis of antigenomic and genomic RNA which are encapsidated and non capped. As a consequence of the use of the same enzyme for both transcription and replication, these mechanisms need to be well coordinated. These processes may be regulated by proteins N and Z in a dose-dependent manner.[PIRNR:PIRNR000836]
		+
		+	==See Also==
		+	*[[RNA polymerase\|RNA polymerase]]
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Lcmv]]
	[[Category: RNA-directed RNA polymerase]]		[[Category: RNA-directed RNA polymerase]]
	[[Category: Alvarez, K]]		[[Category: Alvarez, K]]

OCA at 05:19, 6 October 2017

OCA — Fri, 06 Oct 2017 05:19:44 GMT

←Older revision		Revision as of 05:19, 6 October 2017
Line 1:		Line 1:
-	'''Unreleased structure'''

-	~~The entry~~ 5lts ~~is ON HOLD until Paper Publication~~	+	==Crystal structure of Lymphocytic choriomeningitis mammarenavirus endonuclease Mutant D118A==
-		+	<StructureSection load='5lts' size='340' side='right' caption='[[5lts]], [[Resolution\|resolution]] 2.51Å' scene=''>
-	~~Authors~~: ~~Saez~~-~~Ayala, M~~., ~~Yekwa~~, E.L., ~~Canard~~, B., ~~Alvarez~~, K., ~~Ferron~~, F.	+	== Structural highlights ==
-		+	<table><tr><td colspan='2'>[[5lts]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5LTS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5LTS FirstGlance]. <br>
-	~~Description~~: ~~Crystal structure~~ of ~~Lymphocytic choriomeningitis mammarenavirus endonuclease Mutant D118A~~	+	</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=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr>
-	[[Category: ~~Unreleased Structures~~]]	+	<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5ltf\|5ltf]], [[5ltn\|5ltn]], [[5t2t\|5t2t]]</td></tr>
		+	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/RNA-directed_RNA_polymerase RNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.48 2.7.7.48] </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=5lts FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5lts OCA], [http://pdbe.org/5lts PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5lts RCSB], [http://www.ebi.ac.uk/pdbsum/5lts PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5lts ProSAT]</span></td></tr>
		+	</table>
		+	== Function ==
		+	[[http://www.uniprot.org/uniprot/A0A059U382_9VIRU A0A059U382_9VIRU]] RNA-dependent RNA polymerase which is responsible for replication and transcription of the viral RNA genome. During transcription, synthesizes 4 subgenomic RNAs, and assures their capping by a cap-snatching mechanism, in which cellular capped pre-mRNA are used to generate primers for viral transcription. The 3'-end of subgenomic mRNAs molecules are heterogeneous and not polyadenylated. The replicase function is to direct synthesis of antigenomic and genomic RNA which are encapsidated and non capped. As a consequence of the use of the same enzyme for both transcription and replication, these mechanisms need to be well coordinated. These processes may be regulated by proteins N and Z in a dose-dependent manner.[PIRNR:PIRNR000836]
		+	__TOC__
		+	</StructureSection>
		+	[[Category: RNA-directed RNA polymerase]]
		+	[[Category: Alvarez, K]]
	[[Category: Canard, B]]		[[Category: Canard, B]]
-	[[Category: Yekwa, E.L]]
	[[Category: Ferron, F]]		[[Category: Ferron, F]]
-	[[Category: Alvarez, K]]
	[[Category: Saez-Ayala, M]]		[[Category: Saez-Ayala, M]]
		+	[[Category: Yekwa, E L]]
		+	[[Category: Endonuclease]]
		+	[[Category: Lcmv arenavirus]]
		+	[[Category: Transferase]]

OCA at 14:42, 3 October 2016

OCA — Mon, 03 Oct 2016 14:42:03 GMT

←Older revision		Revision as of 14:42, 3 October 2016
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

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

	Authors: Saez-Ayala, M., Yekwa, E.L., Canard, B., Alvarez, K., Ferron, F.		Authors: Saez-Ayala, M., Yekwa, E.L., Canard, B., Alvarez, K., Ferron, F.

OCA at 11:48, 21 September 2016

OCA — Wed, 21 Sep 2016 11:48:54 GMT

←Older revision		Revision as of 11:48, 21 September 2016
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 5lts is ON HOLD ~~until sometime in the future~~	+	The entry 5lts is ON HOLD

	Authors: Saez-Ayala, M., Yekwa, E.L., Canard, B., Alvarez, K., Ferron, F.		Authors: Saez-Ayala, M., Yekwa, E.L., Canard, B., Alvarez, K., Ferron, F.

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

OCA — Wed, 14 Sep 2016 13:41:10 GMT

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

←Older revision

Revision as of 13:41, 14 September 2016

OCA: New page: '''Unreleased structure''' The entry 5lts is ON HOLD until sometime in the future Authors: Saez-Ayala, M., Yekwa, E.L., Canard, B., Alvarez, K., Ferron, F. Description: Crystal structu...

OCA — Wed, 14 Sep 2016 13:41:09 GMT

New page: '''Unreleased structure''' The entry 5lts is ON HOLD until sometime in the future Authors: Saez-Ayala, M., Yekwa, E.L., Canard, B., Alvarez, K., Ferron, F. Description: Crystal structu...

New page

'''Unreleased structure'''

The entry 5lts is ON HOLD until sometime in the future

Authors: Saez-Ayala, M., Yekwa, E.L., Canard, B., Alvarez, K., Ferron, F.

Description: Crystal structure of Lymphocytic choriomeningitis mammarenavirus endonuclease Mutant D118A
[[Category: Unreleased Structures]]
[[Category: Canard, B]]
[[Category: Yekwa, E.L]]
[[Category: Ferron, F]]
[[Category: Alvarez, K]]
[[Category: Saez-Ayala, M]]