5d6v - Revision history

OCA at 12:23, 6 March 2024

2024-03-06T12:23:05Z

←Older revision		Revision as of 12:23, 6 March 2024
Line 4:		Line 4:
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[5d6v]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Salmonella_enterica_subsp._enterica_serovar_Typhimurium_str._LT2 Salmonella enterica subsp. enterica serovar Typhimurium str. LT2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D6V FirstGlance]. <br>		<table><tr><td colspan='2'>[[5d6v]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Salmonella_enterica_subsp._enterica_serovar_Typhimurium_str._LT2 Salmonella enterica subsp. enterica serovar Typhimurium str. LT2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D6V FirstGlance]. <br>
-	</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [https://pdbe.org/5d6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [https://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></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]] 1.5Å</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [https://pdbe.org/5d6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [https://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
	[https://www.uniprot.org/uniprot/PDUJ_SALTY PDUJ_SALTY] One of the major shell proteins of the bacterial microcompartment (BMC) dedicated to 1,2-propanediol (1,2-PD) degradation. The isolated BMC shell component protein ratio for J:A:B':B:K:T:U is approximately 15:10:7:6:1:1:2 (PubMed:12923081). At least one of PduA or PduJ is required for BMC assembly; it must be encoded as the first gene in the pdu operon (PubMed:33227310, PubMed:27561553). Required for structural integrity of BMCs and to mitigate propionaldehyde toxicity, probably joins facets responsible for BMC closure (PubMed:21239588). Edge residues (particularly Lys-25) are important for function and assembly of the BMC (PubMed:24747050). 80% identical to PduA; although their pore regions appear structurally identical, unlike PduA plays no role in 1,2-PD diffusion into or out of the BMC shell. If pduJ is cloned in the chromosomal position of pduA it is able to complement a pduA deletion; it then has a functional pore as it assumes the transport functions of PduA (PubMed:27561553). Overexpression of this protein leads to aberrant filaments that extend the length of the cell, cross the cleavage furrow and impair division. The filaments form nanotubes with a hollow center (PubMed:33227310). Modeling suggests PduJ is probably the hub for binding multiple enzymes to the interior of the BMC; modeling suggests PduC, PduD, PduG and PduM are targeted to PduJ (Probable).<ref>PMID:12923081</ref> <ref>PMID:21239588</ref> <ref>PMID:24747050</ref> <ref>PMID:27561553</ref> <ref>PMID:33227310</ref> <ref>PMID:25646976</ref> The 1,2-propanediol (1,2-PD) degradation bacterial microcompartment (BMC) concentrates low levels of 1,2-PD catabolic enzymes, concentrates volatile reaction intermediates thus enhancing pathway flux and keeps the level of toxic, mutagenic propionaldehyde low.<ref>PMID:18296526</ref> <ref>PMID:28475631</ref>		[https://www.uniprot.org/uniprot/PDUJ_SALTY PDUJ_SALTY] One of the major shell proteins of the bacterial microcompartment (BMC) dedicated to 1,2-propanediol (1,2-PD) degradation. The isolated BMC shell component protein ratio for J:A:B':B:K:T:U is approximately 15:10:7:6:1:1:2 (PubMed:12923081). At least one of PduA or PduJ is required for BMC assembly; it must be encoded as the first gene in the pdu operon (PubMed:33227310, PubMed:27561553). Required for structural integrity of BMCs and to mitigate propionaldehyde toxicity, probably joins facets responsible for BMC closure (PubMed:21239588). Edge residues (particularly Lys-25) are important for function and assembly of the BMC (PubMed:24747050). 80% identical to PduA; although their pore regions appear structurally identical, unlike PduA plays no role in 1,2-PD diffusion into or out of the BMC shell. If pduJ is cloned in the chromosomal position of pduA it is able to complement a pduA deletion; it then has a functional pore as it assumes the transport functions of PduA (PubMed:27561553). Overexpression of this protein leads to aberrant filaments that extend the length of the cell, cross the cleavage furrow and impair division. The filaments form nanotubes with a hollow center (PubMed:33227310). Modeling suggests PduJ is probably the hub for binding multiple enzymes to the interior of the BMC; modeling suggests PduC, PduD, PduG and PduM are targeted to PduJ (Probable).<ref>PMID:12923081</ref> <ref>PMID:21239588</ref> <ref>PMID:24747050</ref> <ref>PMID:27561553</ref> <ref>PMID:33227310</ref> <ref>PMID:25646976</ref> The 1,2-propanediol (1,2-PD) degradation bacterial microcompartment (BMC) concentrates low levels of 1,2-PD catabolic enzymes, concentrates volatile reaction intermediates thus enhancing pathway flux and keeps the level of toxic, mutagenic propionaldehyde low.<ref>PMID:18296526</ref> <ref>PMID:28475631</ref>
-	<div style="background-color:#fffaf0;">
-	== Publication Abstract from PubMed ==
-	Bacterial microcompartments (MCPs) are complex organelles that consist of metabolic enzymes encapsulated within a protein shell. In this study, we investigate the function of the PduJ MCP shell protein. PduJ is 80% identical in amino acid sequence to PduA and both are major shell proteins of the 1,2-propanediol (1,2-PD) utilization (Pdu) MCP of Salmonella. Prior studies showed that PduA mediates the transport of 1,2-PD (the substrate) into the Pdu MCP. Surprisingly, however, results presented here establish that PduJ has no role 1,2-PD transport. The crystal structure revealed that PduJ was nearly identical to that of PduA and, hence, offered no explanation for their differential functions. Interestingly, however, when a pduJ gene was placed at the pduA chromosomal locus, the PduJ protein acquired a new function, the ability to mediate 1,2-PD transport into the Pdu MCP. To our knowledge, these are the first studies to show that that gene location can determine the function of a MCP shell protein. We propose that gene location dictates protein-protein interactions essential to the function of the MCP shell.
-
-	The function of the PduJ microcompartment shell protein is determined by the genomic position of its encoding gene.,Chowdhury C, Chun S, Sawaya MR, Yeates TO, Bobik TA Mol Microbiol. 2016 Sep;101(5):770-83. doi: 10.1111/mmi.13423. Epub 2016 Jun 7. PMID:27561553<ref>PMID:27561553</ref>
-
-	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
-	</div>
-	<div class="pdbe-citations 5d6v" style="background-color:#fffaf0;"></div>
	== References ==		== References ==
	<references/>		<references/>

OCA at 10:24, 21 June 2023

2023-06-21T10:24:00Z

←Older revision		Revision as of 10:24, 21 June 2023
Line 3:		Line 3:
	<StructureSection load='5d6v' size='340' side='right'caption='[[5d6v]], [[Resolution\|resolution]] 1.50Å' scene=''>		<StructureSection load='5d6v' size='340' side='right'caption='[[5d6v]], [[Resolution\|resolution]] 1.50Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5d6v]] is a 1 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Salty Salty~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D6V OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=5D6V FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5d6v]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Salmonella_enterica_subsp._enterica_serovar_Typhimurium_str._LT2 Salmonella enterica subsp. enterica serovar Typhimurium str. LT2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D6V FirstGlance]. <br>
-	</td></tr>~~<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">pduJ ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=99287 SALTY])</td></tr>~~	+	</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [https://pdbe.org/5d6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [https://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v 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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [~~http~~://pdbe.org/5d6v PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></td></tr>	+
	</table>		</table>
		+	== Function ==
		+	[https://www.uniprot.org/uniprot/PDUJ_SALTY PDUJ_SALTY] One of the major shell proteins of the bacterial microcompartment (BMC) dedicated to 1,2-propanediol (1,2-PD) degradation. The isolated BMC shell component protein ratio for J:A:B':B:K:T:U is approximately 15:10:7:6:1:1:2 (PubMed:12923081). At least one of PduA or PduJ is required for BMC assembly; it must be encoded as the first gene in the pdu operon (PubMed:33227310, PubMed:27561553). Required for structural integrity of BMCs and to mitigate propionaldehyde toxicity, probably joins facets responsible for BMC closure (PubMed:21239588). Edge residues (particularly Lys-25) are important for function and assembly of the BMC (PubMed:24747050). 80% identical to PduA; although their pore regions appear structurally identical, unlike PduA plays no role in 1,2-PD diffusion into or out of the BMC shell. If pduJ is cloned in the chromosomal position of pduA it is able to complement a pduA deletion; it then has a functional pore as it assumes the transport functions of PduA (PubMed:27561553). Overexpression of this protein leads to aberrant filaments that extend the length of the cell, cross the cleavage furrow and impair division. The filaments form nanotubes with a hollow center (PubMed:33227310). Modeling suggests PduJ is probably the hub for binding multiple enzymes to the interior of the BMC; modeling suggests PduC, PduD, PduG and PduM are targeted to PduJ (Probable).<ref>PMID:12923081</ref> <ref>PMID:21239588</ref> <ref>PMID:24747050</ref> <ref>PMID:27561553</ref> <ref>PMID:33227310</ref> <ref>PMID:25646976</ref> The 1,2-propanediol (1,2-PD) degradation bacterial microcompartment (BMC) concentrates low levels of 1,2-PD catabolic enzymes, concentrates volatile reaction intermediates thus enhancing pathway flux and keeps the level of toxic, mutagenic propionaldehyde low.<ref>PMID:18296526</ref> <ref>PMID:28475631</ref>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 21:		Line 22:
	</StructureSection>		</StructureSection>
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: ~~Salty~~]]	+	[[Category: Salmonella enterica subsp. enterica serovar Typhimurium str. LT2]]
-	[[Category: Chun, S]]	+	[[Category: Chun S]]
-	[[Category: Sawaya~~, M R~~]]	+	[[Category: Sawaya MR]]
-	[[Category: Yeates~~, T O]]~~	+	[[Category: Yeates TO]]
-	~~[[Category: Bacterial microcompartment shell protein]]~~	+
-	~~[[Category: Structural protein~~]]	+

OCA at 11:19, 25 December 2019

2019-12-25T11:19:11Z

←Older revision		Revision as of 11:19, 25 December 2019
Line 1:		Line 1:

	==PduJ K25A mutant, from Salmonella enterica serovar Typhimurium LT2, PduJ mutant==		==PduJ K25A mutant, from Salmonella enterica serovar Typhimurium LT2, PduJ mutant==
-	<StructureSection load='5d6v' size='340' side='right' caption='[[5d6v]], [[Resolution\|resolution]] 1.50Å' scene=''>	+	<StructureSection load='5d6v' size='340' side='right'caption='[[5d6v]], [[Resolution\|resolution]] 1.50Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5d6v]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D6V OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D6V FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5d6v]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Salty Salty]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D6V OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D6V FirstGlance]. <br>
-	</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [http://pdbe.org/5d6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [http://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></td></tr>	+	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">pduJ ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=99287 SALTY])</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [http://pdbe.org/5d6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [http://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></td></tr>
	</table>		</table>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
Line 19:		Line 20:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Large Structures]]
		+	[[Category: Salty]]
	[[Category: Chun, S]]		[[Category: Chun, S]]
	[[Category: Sawaya, M R]]		[[Category: Sawaya, M R]]

OCA at 04:44, 9 September 2016

2016-09-09T04:44:00Z

←Older revision		Revision as of 04:44, 9 September 2016
Line 6:		Line 6:
	</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [http://pdbe.org/5d6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [http://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></td></tr>		</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [http://pdbe.org/5d6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [http://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></td></tr>
	</table>		</table>
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Bacterial microcompartments (MCPs) are complex organelles that consist of metabolic enzymes encapsulated within a protein shell. In this study, we investigate the function of the PduJ MCP shell protein. PduJ is 80% identical in amino acid sequence to PduA and both are major shell proteins of the 1,2-propanediol (1,2-PD) utilization (Pdu) MCP of Salmonella. Prior studies showed that PduA mediates the transport of 1,2-PD (the substrate) into the Pdu MCP. Surprisingly, however, results presented here establish that PduJ has no role 1,2-PD transport. The crystal structure revealed that PduJ was nearly identical to that of PduA and, hence, offered no explanation for their differential functions. Interestingly, however, when a pduJ gene was placed at the pduA chromosomal locus, the PduJ protein acquired a new function, the ability to mediate 1,2-PD transport into the Pdu MCP. To our knowledge, these are the first studies to show that that gene location can determine the function of a MCP shell protein. We propose that gene location dictates protein-protein interactions essential to the function of the MCP shell.
		+
		+	The function of the PduJ microcompartment shell protein is determined by the genomic position of its encoding gene.,Chowdhury C, Chun S, Sawaya MR, Yeates TO, Bobik TA Mol Microbiol. 2016 Sep;101(5):770-83. doi: 10.1111/mmi.13423. Epub 2016 Jun 7. PMID:27561553<ref>PMID:27561553</ref>
		+
		+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>
		+	<div class="pdbe-citations 5d6v" style="background-color:#fffaf0;"></div>
		+	== References ==
		+	<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>

OCA at 10:20, 13 July 2016

2016-07-13T10:20:39Z

←Older revision		Revision as of 10:20, 13 July 2016
Line 1:		Line 1:
-	'''Unreleased structure'''

-	~~The entry 5d6v is ON HOLD until Paper Publication~~	+	==PduJ K25A mutant, from Salmonella enterica serovar Typhimurium LT2, PduJ mutant==
-		+	<StructureSection load='5d6v' size='340' side='right' caption='[[5d6v]], [[Resolution\|resolution]] 1.50Å' scene=''>
-	~~Authors: Chun, S., Sawaya, M.R., Yeates, T.O.~~	+	== Structural highlights ==
-		+	<table><tr><td colspan='2'>[[5d6v]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D6V OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D6V FirstGlance]. <br>
-	~~Description:~~ PduJ K25A mutant, from Salmonella enterica serovar Typhimurium LT2, PduJ mutant	+	</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=5d6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d6v OCA], [http://pdbe.org/5d6v PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d6v RCSB], [http://www.ebi.ac.uk/pdbsum/5d6v PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5d6v ProSAT]</span></td></tr>
-	[[~~Category: Unreleased Structures~~]]	+	</table>
-	[[~~Category~~: ~~Sawaya, M~~.R]]	+	__TOC__
-	[[~~Category~~: ~~Yeates~~, T.O]]	+	</StructureSection>
	[[Category: Chun, S]]		[[Category: Chun, S]]
		+	[[Category: Sawaya, M R]]
		+	[[Category: Yeates, T O]]
		+	[[Category: Bacterial microcompartment shell protein]]
		+	[[Category: Structural protein]]

OCA at 09:52, 9 September 2015

2015-09-09T09:52:37Z

←Older revision		Revision as of 09:52, 9 September 2015
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 5d6v is ON HOLD	+	The entry 5d6v is ON HOLD until Paper Publication

	Authors: Chun, S., Sawaya, M.R., Yeates, T.O.		Authors: Chun, S., Sawaya, M.R., Yeates, T.O.

OCA: Protected "5d6v" [edit=sysop:move=sysop]

2015-08-20T11:27:22Z

Protected "5d6v" [edit=sysop:move=sysop]

←Older revision

Revision as of 11:27, 20 August 2015

OCA: New page: '''Unreleased structure''' The entry 5d6v is ON HOLD Authors: Chun, S., Sawaya, M.R., Yeates, T.O. Description: PduJ K25A mutant, from Salmonella enterica serovar Typhimurium LT2, PduJ...

2015-08-20T11:27:21Z

New page: '''Unreleased structure''' The entry 5d6v is ON HOLD Authors: Chun, S., Sawaya, M.R., Yeates, T.O. Description: PduJ K25A mutant, from Salmonella enterica serovar Typhimurium LT2, PduJ...

New page

'''Unreleased structure'''

The entry 5d6v is ON HOLD

Authors: Chun, S., Sawaya, M.R., Yeates, T.O.

Description: PduJ K25A mutant, from Salmonella enterica serovar Typhimurium LT2, PduJ mutant
[[Category: Unreleased Structures]]
[[Category: Sawaya, M.R]]
[[Category: Yeates, T.O]]
[[Category: Chun, S]]