6e2x - Revision history

OCA at 14:38, 13 March 2024

OCA — Wed, 13 Mar 2024 14:38:53 GMT

←Older revision		Revision as of 14:38, 13 March 2024
Line 3:		Line 3:
	<SX load='6e2x' size='340' side='right' viewer='molstar' caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>		<SX load='6e2x' size='340' side='right' viewer='molstar' caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Pcv2 Pcv2~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://proteopedia.org/fgij/fg.htm?mol=6E2X FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure with sequence from [https://en.wikipedia.org/wiki/Porcine_circovirus_2 Porcine circovirus 2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6E2X FirstGlance]. <br>
-	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IDS:2-O-SULFO-ALPHA-L-IDOPYRANURONIC+ACID'>IDS</scene>, <scene name='pdbligand=SGN:N,O6-DISULFO-GLUCOSAMINE'>SGN</scene>~~</td></tr>~~	+	</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models\|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution\|Resolution]] 3.5Å</td></tr>
-	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">cap, Cap, cp, ORF2, PCV2_gp3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=85708 PCV2])</td></tr>	+	<tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IDS:2-O-SULFO-ALPHA-L-IDOPYRANURONIC+ACID'>IDS</scene>, <scene name='pdbligand=SGN:N,O6-DISULFO-GLUCOSAMINE'>SGN</scene></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=6e2x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e2x OCA], [~~http~~://pdbe.org/6e2x PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=6e2x RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/6e2x PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=6e2x 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=6e2x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e2x OCA], [https://pdbe.org/6e2x PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6e2x RCSB], [https://www.ebi.ac.uk/pdbsum/6e2x PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6e2x ProSAT]</span></td></tr>
	</table>		</table>
-	~~<div style~~=~~"background-color:#fffaf0;">~~	+	== Function ==
-	=~~= Publication Abstract from PubMed~~ ==	+	[https://www.uniprot.org/uniprot/Q805N7_PCV2 Q805N7_PCV2]
-	~~Porcine circovirus 2 (PCV2) is the smallest pathogenic virus capable of autonomous replication within its host~~. Infections result in immunosuppression and subsequent death of the host and are initiated via the attachment of the PCV2 icosahedral capsid to heparan sulfate (HS) and chondroitin sulfate B (CSB) glycosaminoglycans on the cell surface. However, the underlying mechanism of structural recognition remains to be explored. Using heparin, a routinely used analog of heparan sulfate, we demonstrate that increasing lengths of heparin exhibit a greater affinity toward PCV2. Our competition assays indicate that dextran sulfate (8 kDa) has a higher affinity for PCV2 than heparin (12 kDa), chondroitin sulfate B (41 kDa), hyaluronic acid (1.6 MDa), and dextran (6 kDa). This suggests that polymers high in sulfate content are capable of competing with the PCV2-heparan sulfate interaction and, thus, have the potential to inhibit PCV2 infection. Finally, we visualized the interaction between heparin and the PCV2 capsid using cryo-electron microscopy single-particle analysis, symmetry expansion, and focused classification. The image reconstructions provide the first example of an asymmetric distribution of heparin on the surface of an icosahedral virus capsid. We demonstrate that each of the 60 capsid subunits that generate the T=1 capsid can bind heparin via one of five binding sites. However, not all of the binding sites were occupied by heparin, and only one-third to two-thirds of the binding sites were occupied. The binding sites are defined by arginine, lysine, and polar amino acids. Mutating the arginine, lysine, and polar amino acids to alanine diminished the binding capacity of PCV2 to heparin.IMPORTANCE It has been demonstrated that porcine circovirus 2 (PCV2) attaches to cells via heparan sulfate (HS) and chondroitin sulfate B (CSB) glycosaminoglycans; however, the underlying structural mechanism describing the HS/CSB recognition by PCV2 remains to be explored. We used cryo-electron microscopy with single-particle analysis, symmetry expansion, and focused classification to visualize the interaction between the PCV2 capsid and heparin, an analog of heparan sulfate, to better than 3.6-A resolution. We observed that the interaction between PCV2 and heparin does not adhere to the icosahedral symmetry of the capsid. To the best of our knowledge, this is the first example where the interaction between heparin and an icosahedral capsid does not follow the symmetry elements of the capsid. Our findings also suggest that anionic polymers, such as dextran sulfate, may act to inhibit PCV2 infection.	+

-	Porcine Circovirus 2 Uses a Multitude of Weak Binding Sites To Interact with Heparan Sulfate, and the Interactions Do Not Follow the Symmetry of the Capsid.,Dhindwal S, Avila B, Feng S, Khayat R J Virol. 2019 Mar 5;93(6). pii: JVI.02222-18. doi: 10.1128/JVI.02222-18. Print, 2019 Mar 15. PMID:30602608<ref>PMID:30602608</ref>	+	==See Also==
-		+	*[[Virus coat proteins 3D structures\|Virus coat proteins 3D structures]]
-	~~From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>~~	+
-	~~</div>~~	+
-	~~<div class="pdbe-citations 6e2x" style="background-color:#fffaf0;"></div>~~	+
-	== ~~References~~ ==	+
-	~~<references/>~~	+
	__TOC__		__TOC__
	</SX>		</SX>
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: ~~Pcv2~~]]	+	[[Category: Porcine circovirus 2]]
-	[[Category: Dhindwal, S]]	+	[[Category: Dhindwal S]]
-	[[Category: Khayat, R]]	+	[[Category: Khayat R]]
-	~~[[Category: Viral jelly-roll]]~~	+
-	~~[[Category: Virus like particle~~]]	+

OCA at 00:18, 11 April 2020

OCA — Sat, 11 Apr 2020 00:18:55 GMT

←Older revision		Revision as of 00:18, 11 April 2020
Line 3:		Line 3:
	<SX load='6e2x' size='340' side='right' viewer='molstar' caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>		<SX load='6e2x' size='340' side='right' viewer='molstar' caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure with sequence from [http://en.wikipedia.org/wiki/Pcv2 Pcv2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [http://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=6E2X FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure with sequence from [http://en.wikipedia.org/wiki/Pcv2 Pcv2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6E2X FirstGlance]. <br>
-	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=IDS:2-O-SULFO-ALPHA-L-IDOPYRANURONIC+ACID'>IDS</scene>, <scene name='pdbligand=SGN:N,O6-DISULFO-GLUCOSAMINE'>SGN</scene></td></tr>	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IDS:2-O-SULFO-ALPHA-L-IDOPYRANURONIC+ACID'>IDS</scene>, <scene name='pdbligand=SGN:N,O6-DISULFO-GLUCOSAMINE'>SGN</scene></td></tr>
	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">cap, Cap, cp, ORF2, PCV2_gp3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=85708 PCV2])</td></tr>		<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">cap, Cap, cp, ORF2, PCV2_gp3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=85708 PCV2])</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=6e2x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e2x OCA], [http://pdbe.org/6e2x PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6e2x RCSB], [http://www.ebi.ac.uk/pdbsum/6e2x PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6e2x 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=6e2x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e2x OCA], [http://pdbe.org/6e2x PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6e2x RCSB], [http://www.ebi.ac.uk/pdbsum/6e2x PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6e2x ProSAT]</span></td></tr>
	</table>		</table>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">

OCA at 21:00, 6 March 2020

OCA — Fri, 06 Mar 2020 21:00:44 GMT

←Older revision		Revision as of 21:00, 6 March 2020
Line 1:		Line 1:

	==Mechanism of cellular recognition by PCV2==		==Mechanism of cellular recognition by PCV2==
-	<~~StructureSection~~ load='6e2x' size='340' side='right'caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>	+	<SX load='6e2x' size='340' side='right' viewer='molstar' caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure with sequence from [http://en.wikipedia.org/wiki/Pcv2 Pcv2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6E2X FirstGlance]. <br>		<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure with sequence from [http://en.wikipedia.org/wiki/Pcv2 Pcv2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6E2X FirstGlance]. <br>
Line 20:		Line 20:
	<references/>		<references/>
	__TOC__		__TOC__
-	</~~StructureSection~~>	+	</SX>
	[[Category: Large Structures]]		[[Category: Large Structures]]
	[[Category: Pcv2]]		[[Category: Pcv2]]

OCA at 06:18, 10 July 2019

OCA — Wed, 10 Jul 2019 06:18:10 GMT

←Older revision		Revision as of 06:18, 10 July 2019
Line 1:		Line 1:
-	~~{{Large structure}}~~	+
	==Mechanism of cellular recognition by PCV2==		==Mechanism of cellular recognition by PCV2==
-	<StructureSection load='6e2x' size='340' side='right' caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>	+	<StructureSection load='6e2x' size='340' side='right'caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6E2X FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure with sequence from [http://en.wikipedia.org/wiki/Pcv2 Pcv2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6E2X FirstGlance]. <br>
	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=IDS:2-O-SULFO-ALPHA-L-IDOPYRANURONIC+ACID'>IDS</scene>, <scene name='pdbligand=SGN:N,O6-DISULFO-GLUCOSAMINE'>SGN</scene></td></tr>		</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=IDS:2-O-SULFO-ALPHA-L-IDOPYRANURONIC+ACID'>IDS</scene>, <scene name='pdbligand=SGN:N,O6-DISULFO-GLUCOSAMINE'>SGN</scene></td></tr>
		+	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">cap, Cap, cp, ORF2, PCV2_gp3 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=85708 PCV2])</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=6e2x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e2x OCA], [http://pdbe.org/6e2x PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6e2x RCSB], [http://www.ebi.ac.uk/pdbsum/6e2x PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6e2x 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=6e2x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e2x OCA], [http://pdbe.org/6e2x PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6e2x RCSB], [http://www.ebi.ac.uk/pdbsum/6e2x PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6e2x ProSAT]</span></td></tr>
	</table>		</table>
-	~~{{Large structure}}~~	+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Porcine circovirus 2 (PCV2) is the smallest pathogenic virus capable of autonomous replication within its host. Infections result in immunosuppression and subsequent death of the host and are initiated via the attachment of the PCV2 icosahedral capsid to heparan sulfate (HS) and chondroitin sulfate B (CSB) glycosaminoglycans on the cell surface. However, the underlying mechanism of structural recognition remains to be explored. Using heparin, a routinely used analog of heparan sulfate, we demonstrate that increasing lengths of heparin exhibit a greater affinity toward PCV2. Our competition assays indicate that dextran sulfate (8 kDa) has a higher affinity for PCV2 than heparin (12 kDa), chondroitin sulfate B (41 kDa), hyaluronic acid (1.6 MDa), and dextran (6 kDa). This suggests that polymers high in sulfate content are capable of competing with the PCV2-heparan sulfate interaction and, thus, have the potential to inhibit PCV2 infection. Finally, we visualized the interaction between heparin and the PCV2 capsid using cryo-electron microscopy single-particle analysis, symmetry expansion, and focused classification. The image reconstructions provide the first example of an asymmetric distribution of heparin on the surface of an icosahedral virus capsid. We demonstrate that each of the 60 capsid subunits that generate the T=1 capsid can bind heparin via one of five binding sites. However, not all of the binding sites were occupied by heparin, and only one-third to two-thirds of the binding sites were occupied. The binding sites are defined by arginine, lysine, and polar amino acids. Mutating the arginine, lysine, and polar amino acids to alanine diminished the binding capacity of PCV2 to heparin.IMPORTANCE It has been demonstrated that porcine circovirus 2 (PCV2) attaches to cells via heparan sulfate (HS) and chondroitin sulfate B (CSB) glycosaminoglycans; however, the underlying structural mechanism describing the HS/CSB recognition by PCV2 remains to be explored. We used cryo-electron microscopy with single-particle analysis, symmetry expansion, and focused classification to visualize the interaction between the PCV2 capsid and heparin, an analog of heparan sulfate, to better than 3.6-A resolution. We observed that the interaction between PCV2 and heparin does not adhere to the icosahedral symmetry of the capsid. To the best of our knowledge, this is the first example where the interaction between heparin and an icosahedral capsid does not follow the symmetry elements of the capsid. Our findings also suggest that anionic polymers, such as dextran sulfate, may act to inhibit PCV2 infection.
		+
		+	Porcine Circovirus 2 Uses a Multitude of Weak Binding Sites To Interact with Heparan Sulfate, and the Interactions Do Not Follow the Symmetry of the Capsid.,Dhindwal S, Avila B, Feng S, Khayat R J Virol. 2019 Mar 5;93(6). pii: JVI.02222-18. doi: 10.1128/JVI.02222-18. Print, 2019 Mar 15. PMID:30602608<ref>PMID:30602608</ref>
		+
		+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>
		+	<div class="pdbe-citations 6e2x" style="background-color:#fffaf0;"></div>
		+	== References ==
		+	<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Large Structures]]
		+	[[Category: Pcv2]]
	[[Category: Dhindwal, S]]		[[Category: Dhindwal, S]]
	[[Category: Khayat, R]]		[[Category: Khayat, R]]
	[[Category: Viral jelly-roll]]		[[Category: Viral jelly-roll]]
	[[Category: Virus like particle]]		[[Category: Virus like particle]]

OCA at 08:17, 26 December 2018

OCA — Wed, 26 Dec 2018 08:17:07 GMT

←Older revision		Revision as of 08:17, 26 December 2018
Line 1:		Line 1:
-	'''~~Unreleased structure~~'''	+	{{Large structure}}
-		+	==Mechanism of cellular recognition by PCV2==
-	~~The entry~~ 6e2x is ~~ON HOLD until Paper Publication~~	+	<StructureSection load='6e2x' size='340' side='right' caption='[[6e2x]], [[Resolution\|resolution]] 3.50Å' scene=''>
-		+	== Structural highlights ==
-	~~Authors~~: ~~Khayat~~, R., ~~Dhindwal~~, S.	+	<table><tr><td colspan='2'>[[6e2x]] is a 60 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6E2X OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6E2X FirstGlance]. <br>
-		+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=IDS:2-O-SULFO-ALPHA-L-IDOPYRANURONIC+ACID'>IDS</scene>, <scene name='pdbligand=SGN:N,O6-DISULFO-GLUCOSAMINE'>SGN</scene></td></tr>
-	~~Description~~: ~~Mechanism of cellular recognition by PCV2~~	+	<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=6e2x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6e2x OCA], [http://pdbe.org/6e2x PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6e2x RCSB], [http://www.ebi.ac.uk/pdbsum/6e2x PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6e2x ProSAT]</span></td></tr>
-	[~~[Category~~: ~~Unreleased Structures]~~]	+	</table>
		+	{{Large structure}}
		+	__TOC__
		+	</StructureSection>
	[[Category: Dhindwal, S]]		[[Category: Dhindwal, S]]
	[[Category: Khayat, R]]		[[Category: Khayat, R]]
		+	[[Category: Viral jelly-roll]]
		+	[[Category: Virus like particle]]

OCA at 19:48, 9 August 2018

OCA — Thu, 09 Aug 2018 19:48:50 GMT

←Older revision		Revision as of 19:48, 9 August 2018
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 6e2x is ON HOLD	+	The entry 6e2x is ON HOLD until Paper Publication

	Authors: Khayat, R., Dhindwal, S.		Authors: Khayat, R., Dhindwal, S.

OCA: Protected "6e2x" [edit=sysop:move=sysop]

OCA — Wed, 18 Jul 2018 05:43:57 GMT

Protected "6e2x" [edit=sysop:move=sysop]

←Older revision

Revision as of 05:43, 18 July 2018

OCA: New page: '''Unreleased structure''' The entry 6e2x is ON HOLD Authors: Khayat, R., Dhindwal, S. Description: Mechanism of cellular recognition by PCV2 Category: Unreleased Structures [[Cate...

OCA — Wed, 18 Jul 2018 05:43:55 GMT

New page: '''Unreleased structure''' The entry 6e2x is ON HOLD Authors: Khayat, R., Dhindwal, S. Description: Mechanism of cellular recognition by PCV2 Category: Unreleased Structures [[Cate...

New page

'''Unreleased structure'''

The entry 6e2x is ON HOLD

Authors: Khayat, R., Dhindwal, S.

Description: Mechanism of cellular recognition by PCV2
[[Category: Unreleased Structures]]
[[Category: Dhindwal, S]]
[[Category: Khayat, R]]