4mzl - Revision history

OCA at 10:22, 28 December 2022

OCA — Wed, 28 Dec 2022 10:22:08 GMT

←Older revision		Revision as of 10:22, 28 December 2022
Line 1:		Line 1:

	==Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a hydrogen bond surrogate myoA helix mimetic==		==Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a hydrogen bond surrogate myoA helix mimetic==
-	<StructureSection load='4mzl' size='340' side='right' caption='[[4mzl]], [[Resolution\|resolution]] 2.01Å' scene=''>	+	<StructureSection load='4mzl' size='340' side='right'caption='[[4mzl]], [[Resolution\|resolution]] 2.01Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[4mzl]] is a 4 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Plaf7 Plaf7~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MZL OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=4MZL FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[4mzl]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Plasmodium_falciparum_3D7 Plasmodium falciparum 3D7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MZL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4MZL FirstGlance]. <br>
-	</td></tr><tr id='~~NonStdRes~~'><td class="sblockLbl"><b>[[~~Non-Standard_Residue~~\|~~NonStd Res~~:]]</b></td><td class="sblockDat"><scene name='pdbligand=2JC:N-ETHYLGLYCINE'>2JC</scene>, <scene name='pdbligand=BUA:BUTANOIC+ACID'>BUA</scene>~~</td></tr>~~	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=2JC:N-ETHYLGLYCINE'>2JC</scene>, <scene name='pdbligand=BUA:BUTANOIC+ACID'>BUA</scene></td></tr>
-	~~<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4aom\|4aom]], [[4mzk\|4mzk]], [[4mzj\|4mzj]]</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=4mzl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mzl OCA], [https://pdbe.org/4mzl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4mzl RCSB], [https://www.ebi.ac.uk/pdbsum/4mzl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4mzl ProSAT]</span></td></tr>
-	~~<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">MTIP, PFL2225w ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=36329 PLAF7])~~</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=4mzl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mzl OCA], [~~http~~://pdbe.org/4mzl PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=4mzl RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/4mzl PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=4mzl ProSAT]</span></td></tr>	+
	</table>		</table>
	== Function ==		== Function ==
-	[~~[http~~://www.uniprot.org/uniprot/~~MYOA_PLAF7 MYOA_PLAF7~~]] Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments (By similarity).	+	[https://www.uniprot.org/uniprot/Q8I4W8_PLAF7 Q8I4W8_PLAF7]
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 24:		Line 22:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Plaf7~~]]	+	[[Category: Large Structures]]
-	[[Category: ~~Cota, E~~]]	+	[[Category: Plasmodium falciparum 3D7]]
-	[[Category: ~~Douse, C H]]~~	+	[[Category: Cota E]]
-	~~[[Category: Garnett, J A]]~~	+	[[Category: Douse CH]]
-	~~[[Category: Maas, S J]]~~	+	[[Category: Garnett JA]]
-	~~[[Category: Tate,~~ E W]]	+	[[Category: Maas SJ]]
-	[[Category: ~~Actomyosin motor~~]]	+	[[Category: Tate EW]]
-	[[Category: ~~Alpha-helix mimetic~~]]	+
-	[[Category: ~~Protein binding-inhibitor complex~~]]	+
-	[[Category: ~~Stapled peptide~~]]	+

OCA at 17:40, 4 August 2016

OCA — Thu, 04 Aug 2016 17:40:09 GMT

←Older revision		Revision as of 17:40, 4 August 2016
Line 1:		Line 1:
		+
	==Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a hydrogen bond surrogate myoA helix mimetic==		==Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a hydrogen bond surrogate myoA helix mimetic==
	<StructureSection load='4mzl' size='340' side='right' caption='[[4mzl]], [[Resolution\|resolution]] 2.01Å' scene=''>		<StructureSection load='4mzl' size='340' side='right' caption='[[4mzl]], [[Resolution\|resolution]] 2.01Å' scene=''>
Line 6:		Line 7:
	<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4aom\|4aom]], [[4mzk\|4mzk]], [[4mzj\|4mzj]]</td></tr>		<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4aom\|4aom]], [[4mzk\|4mzk]], [[4mzj\|4mzj]]</td></tr>
	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">MTIP, PFL2225w ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=36329 PLAF7])</td></tr>		<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">MTIP, PFL2225w ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=36329 PLAF7])</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=4mzl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mzl OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4mzl RCSB], [http://www.ebi.ac.uk/pdbsum/4mzl PDBsum]</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=4mzl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mzl OCA], [http://pdbe.org/4mzl PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4mzl RCSB], [http://www.ebi.ac.uk/pdbsum/4mzl PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4mzl ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
Line 18:		Line 19:
	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>		From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
	</div>		</div>
		+	<div class="pdbe-citations 4mzl" style="background-color:#fffaf0;"></div>
	== References ==		== References ==
	<references/>		<references/>

OCA at 17:43, 24 December 2014

OCA — Wed, 24 Dec 2014 17:43:22 GMT

←Older revision		Revision as of 17:43, 24 December 2014
Line 3:		Line 3:
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4mzl]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Plaf7 Plaf7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MZL OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MZL FirstGlance]. <br>		<table><tr><td colspan='2'>[[4mzl]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Plaf7 Plaf7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MZL OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MZL FirstGlance]. <br>
-	</td></tr><tr><td class="sblockLbl"><b>[[Non-Standard_Residue\|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=2JC:N-ETHYLGLYCINE'>2JC</scene>, <scene name='pdbligand=BUA:BUTANOIC+ACID'>BUA</scene></td></tr>	+	</td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue\|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=2JC:N-ETHYLGLYCINE'>2JC</scene>, <scene name='pdbligand=BUA:BUTANOIC+ACID'>BUA</scene></td></tr>
-	<tr><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4aom\|4aom]], [[4mzk\|4mzk]], [[4mzj\|4mzj]]</td></tr>	+	<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4aom\|4aom]], [[4mzk\|4mzk]], [[4mzj\|4mzj]]</td></tr>
-	<tr><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">MTIP, PFL2225w ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=36329 PLAF7])</td></tr>	+	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">MTIP, PFL2225w ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=36329 PLAF7])</td></tr>
-	<tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4mzl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mzl OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4mzl RCSB], [http://www.ebi.ac.uk/pdbsum/4mzl PDBsum]</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=4mzl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mzl OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4mzl RCSB], [http://www.ebi.ac.uk/pdbsum/4mzl PDBsum]</span></td></tr>
-	<table>	+	</table>
		+	== Function ==
		+	[[http://www.uniprot.org/uniprot/MYOA_PLAF7 MYOA_PLAF7]] Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments (By similarity).
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 21:		Line 23:
	</StructureSection>		</StructureSection>
	[[Category: Plaf7]]		[[Category: Plaf7]]
-	[[Category: Cota, E.]]	+	[[Category: Cota, E]]
-	[[Category: Douse, C H.]]	+	[[Category: Douse, C H]]
-	[[Category: Garnett, J A.]]	+	[[Category: Garnett, J A]]
-	[[Category: Maas, S J.]]	+	[[Category: Maas, S J]]
-	[[Category: Tate, E W.]]	+	[[Category: Tate, E W]]
	[[Category: Actomyosin motor]]		[[Category: Actomyosin motor]]
	[[Category: Alpha-helix mimetic]]		[[Category: Alpha-helix mimetic]]
	[[Category: Protein binding-inhibitor complex]]		[[Category: Protein binding-inhibitor complex]]
	[[Category: Stapled peptide]]		[[Category: Stapled peptide]]

OCA at 02:53, 4 September 2014

OCA — Thu, 04 Sep 2014 02:53:05 GMT

←Older revision		Revision as of 02:53, 4 September 2014
Line 10:		Line 10:
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
-	~~By using a phage display derived peptide as an initial template, compounds have been developed that~~ are ~~highly specific against Mdm2/Mdm4. These compounds exhibit greater potency in p53 activation and~~ protein-protein ~~interaction assays than~~ a ~~compound derived from the p53 wild~~-~~type sequence~~. ~~Unlike Nutlin,~~ a ~~small molecule inhibitor~~ of ~~Mdm2/Mdm4~~, the ~~phage derived compounds can arrest cells resistant~~ to ~~p53 induced apoptosis over~~ a ~~wide concentration range without cellular toxicity~~, ~~suggesting they are highly suitable for cyclotherapy~~.	+	Constrained alpha-helical peptides are an exciting class of molecule designed to disrupt protein-protein interactions (PPIs) at a surface-exposed helix binding site. Complexes that engage more than one helical face account for over a third of structurally characterized helix PPIs, including several examples where the helix is fully buried. However, no constrained peptides have been reported that have targeted this class of interaction. We report the design of stapled and hydrogen bond surrogate (HBS) peptides mimicking the helical tail of the malaria parasite invasion motor myosin (myoA), which presents polar and hydrophobic functionality on all three faces in binding its partner, myoA tail interacting protein (MTIP), with high affinity. The first structures of these different constrained peptides bound to the same target are reported, enabling a direct comparison between these constraints and between staples based on monosubstituted pentenyl glycine (pGly) and disubstituted pentenyl alanine (pAla). Importantly, installation of these constraints does not disrupt native interactions in the buried site, so the affinity of the wild-type peptide is maintained.

-	Stapled ~~peptides with improved potency~~ and ~~specificity that activate p53~~.,~~Brown CJ~~, ~~Quah ST~~, ~~Jong J~~, ~~Goh AM~~, ~~Chiam PC~~, ~~Khoo KH~~, ~~Choong ML, Lee MA, Yurlova L, Zolghadr K, Joseph TL, Verma CS, Lane DP~~ ACS Chem Biol. ~~2013 Mar 15;8(3):506-12. doi: 10.1021/cb3005148. Epub 2012 Dec 18~~. PMID:~~23214419~~<ref>PMID:~~23214419~~</ref>	+	Crystal Structures of Stapled and Hydrogen Bond Surrogate Peptides Targeting a Fully Buried Protein-Helix Interaction.,Douse CH, Maas SJ, Thomas JC, Garnett JA, Sun Y, Cota E, Tate EW ACS Chem Biol. 2014 Aug 6. PMID:25084543<ref>PMID:25084543</ref>

	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>		From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>

OCA at 13:17, 20 August 2014

OCA — Wed, 20 Aug 2014 13:17:00 GMT

←Older revision		Revision as of 13:17, 20 August 2014
Line 1:		Line 1:
-	~~{{STRUCTURE_4mzl\| PDB=4mzl \| SCENE= }}~~	+	==Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a hydrogen bond surrogate myoA helix mimetic==
-	===Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a hydrogen bond surrogate myoA helix mimetic===	+	<StructureSection load='4mzl' size='340' side='right' caption='[[4mzl]], [[Resolution\|resolution]] 2.01Å' scene=''>
		+	== Structural highlights ==
		+	<table><tr><td colspan='2'>[[4mzl]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Plaf7 Plaf7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MZL OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MZL FirstGlance]. <br>
		+	</td></tr><tr><td class="sblockLbl"><b>[[Non-Standard_Residue\|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=2JC:N-ETHYLGLYCINE'>2JC</scene>, <scene name='pdbligand=BUA:BUTANOIC+ACID'>BUA</scene></td></tr>
		+	<tr><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4aom\|4aom]], [[4mzk\|4mzk]], [[4mzj\|4mzj]]</td></tr>
		+	<tr><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">MTIP, PFL2225w ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=36329 PLAF7])</td></tr>
		+	<tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4mzl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mzl OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4mzl RCSB], [http://www.ebi.ac.uk/pdbsum/4mzl PDBsum]</span></td></tr>
		+	<table>
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	By using a phage display derived peptide as an initial template, compounds have been developed that are highly specific against Mdm2/Mdm4. These compounds exhibit greater potency in p53 activation and protein-protein interaction assays than a compound derived from the p53 wild-type sequence. Unlike Nutlin, a small molecule inhibitor of Mdm2/Mdm4, the phage derived compounds can arrest cells resistant to p53 induced apoptosis over a wide concentration range without cellular toxicity, suggesting they are highly suitable for cyclotherapy.

-	~~==Function==~~	+	Stapled peptides with improved potency and specificity that activate p53.,Brown CJ, Quah ST, Jong J, Goh AM, Chiam PC, Khoo KH, Choong ML, Lee MA, Yurlova L, Zolghadr K, Joseph TL, Verma CS, Lane DP ACS Chem Biol. 2013 Mar 15;8(3):506-12. doi: 10.1021/cb3005148. Epub 2012 Dec 18. PMID:23214419<ref>PMID:23214419</ref>
-	~~[[http://www.uniprot.org/uniprot/MYOA_PLAF7 MYOA_PLAF7]] Myosins are actin-based motor molecules~~ with ~~ATPase activity~~. ~~Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments~~, ~~which would be moved relative to actin filaments~~ (~~By similarity~~).	+

-	==~~About this Structure~~==	+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
-	~~[[4mzl]] is a 4 chain structure with sequence from [http:~~//~~en.wikipedia.org/wiki/Plasmodium_falciparum_3d7 Plasmodium falciparum 3d7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MZL OCA].~~	+	</div>
-	[[Category: ~~Plasmodium falciparum 3d7~~]]	+	== References ==
		+	<references/>
		+	__TOC__
		+	</StructureSection>
		+	[[Category: Plaf7]]
	[[Category: Cota, E.]]		[[Category: Cota, E.]]
	[[Category: Douse, C H.]]		[[Category: Douse, C H.]]

OCA at 07:55, 6 November 2013

OCA — Wed, 06 Nov 2013 07:55:00 GMT

←Older revision		Revision as of 07:55, 6 November 2013
Line 1:		Line 1:
-	~~'''Unreleased structure'''~~	+	{{STRUCTURE_4mzl\| PDB=4mzl \| SCENE= }}
		+	===Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a hydrogen bond surrogate myoA helix mimetic===

-	~~The entry 4mzl is ON HOLD until sometime~~ in ~~the future~~	+	==Function==
		+	[[http://www.uniprot.org/uniprot/MYOA_PLAF7 MYOA_PLAF7]] Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments (By similarity).

-	~~Authors~~: Douse, C.H., Garnett, J.A., Maas, S.J.~~, Cota, E.,~~ Tate, E.W.	+	==About this Structure==
-		+	[[4mzl]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Plasmodium_falciparum_3d7 Plasmodium falciparum 3d7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MZL OCA].
-	~~Description~~: ~~Crystal Structure of MTIP from Plasmodium falciparum in~~ complex ~~with HBS myoA, a stapled myoA tail~~ peptide	+	[[Category: Plasmodium falciparum 3d7]]
		+	[[Category: Cota, E.]]
		+	[[Category: Douse, C H.]]
		+	[[Category: Garnett, J A.]]
		+	[[Category: Maas, S J.]]
		+	[[Category: Tate, E W.]]
		+	[[Category: Actomyosin motor]]
		+	[[Category: Alpha-helix mimetic]]
		+	[[Category: Protein binding-inhibitor complex]]
		+	[[Category: Stapled peptide]]

OCA at 07:30, 16 October 2013

OCA — Wed, 16 Oct 2013 07:30:27 GMT

←Older revision		Revision as of 07:30, 16 October 2013
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 4mzl is ON HOLD	+	The entry 4mzl is ON HOLD until sometime in the future

	Authors: Douse, C.H., Garnett, J.A., Maas, S.J., Cota, E., Tate, E.W.		Authors: Douse, C.H., Garnett, J.A., Maas, S.J., Cota, E., Tate, E.W.

	Description: Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a stapled myoA tail peptide		Description: Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a stapled myoA tail peptide

OCA: Protected "4mzl" [edit=sysop:move=sysop]

OCA — Thu, 10 Oct 2013 05:51:47 GMT

Protected "4mzl" [edit=sysop:move=sysop]

←Older revision

Revision as of 05:51, 10 October 2013

OCA: New page: '''Unreleased structure''' The entry 4mzl is ON HOLD Authors: Douse, C.H., Garnett, J.A., Maas, S.J., Cota, E., Tate, E.W. Description: Crystal Structure of MTIP from Plasmodium falcip...

OCA — Thu, 10 Oct 2013 05:51:47 GMT

New page: '''Unreleased structure''' The entry 4mzl is ON HOLD Authors: Douse, C.H., Garnett, J.A., Maas, S.J., Cota, E., Tate, E.W. Description: Crystal Structure of MTIP from Plasmodium falcip...

New page

'''Unreleased structure'''

The entry 4mzl is ON HOLD

Authors: Douse, C.H., Garnett, J.A., Maas, S.J., Cota, E., Tate, E.W.

Description: Crystal Structure of MTIP from Plasmodium falciparum in complex with HBS myoA, a stapled myoA tail peptide