4mac - Revision history

OCA at 08:56, 20 March 2024

2024-03-20T08:56:06Z

← Older revision		Revision as of 08:56, 20 March 2024
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	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4MAC FirstGlance]. <br>		<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4MAC 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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [https://pdbe.org/4mac PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [https://www.ebi.ac.uk/pdbsum/4mac PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4mac 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]] 2Å</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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [https://pdbe.org/4mac PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [https://www.ebi.ac.uk/pdbsum/4mac PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4mac ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
	[https://www.uniprot.org/uniprot/CIDEC_MOUSE CIDEC_MOUSE] Binds to lipid droplets and regulates their enlargement, thereby restricting lipolysis and favoring storage. At focal contact sites between lipid droplets, promotes directional net neutral lipid transfer from the smaller to larger lipid droplets. The transfer direction may be driven by the internal pressure difference between the contacting lipid droplet pair. Its role in neutral lipid transfer and lipid droplet enlargement is activated by the interaction with PLIN1. May act as a CEBPB coactivator in the white adipose tissue to control the expression of a subset of CEBPB downstream target genes, including SOCS1, SOCS3, TGFB1, TGFBR1, ID2 and XDH. When overexpressed in preadipocytes, induces apoptosis or increases cell susceptibility to apoptosis induced by serum deprivation or TGFB treatment. As mature adipocytes, that express high CIDEC levels, are quite resistant to apoptotic stimuli, the physiological significance of its role in apoptosis is unclear. May play a role in the modulation of the response to osmotic stress by preventing NFAT5 to translocate into the nucleus and activate its target genes expression.<ref>PMID:18334488</ref> <ref>PMID:22144693</ref> <ref>PMID:22245780</ref> <ref>PMID:23481402</ref>		[https://www.uniprot.org/uniprot/CIDEC_MOUSE CIDEC_MOUSE] Binds to lipid droplets and regulates their enlargement, thereby restricting lipolysis and favoring storage. At focal contact sites between lipid droplets, promotes directional net neutral lipid transfer from the smaller to larger lipid droplets. The transfer direction may be driven by the internal pressure difference between the contacting lipid droplet pair. Its role in neutral lipid transfer and lipid droplet enlargement is activated by the interaction with PLIN1. May act as a CEBPB coactivator in the white adipose tissue to control the expression of a subset of CEBPB downstream target genes, including SOCS1, SOCS3, TGFB1, TGFBR1, ID2 and XDH. When overexpressed in preadipocytes, induces apoptosis or increases cell susceptibility to apoptosis induced by serum deprivation or TGFB treatment. As mature adipocytes, that express high CIDEC levels, are quite resistant to apoptotic stimuli, the physiological significance of its role in apoptosis is unclear. May play a role in the modulation of the response to osmotic stress by preventing NFAT5 to translocate into the nucleus and activate its target genes expression.<ref>PMID:18334488</ref> <ref>PMID:22144693</ref> <ref>PMID:22245780</ref> <ref>PMID:23481402</ref>
	~~<div style="background-color:#fffaf0;">~~
	~~== Publication Abstract from PubMed ==~~
	FSP27 (CIDE-3 in humans) plays critical roles in lipid metabolism and apoptosis and is known to be involved in regulation of lipid droplet (LD) size and lipid storage and apoptotic DNA fragmentation. Given that CIDE-containing proteins including FSP27 are associated with many human diseases including cancer, aging, diabetes, and obesity, studies of FSP27 and other CIDE-containing proteins are of great biological importance. As a first step toward elucidating the molecular mechanisms of FSP27-mediated lipid droplet growth and apoptosis, we report the crystal structure of the CIDE-N domain of FSP27 at a resolution of 2.0 A. The structure revealed a possible biologically important homo-dimeric interface similar to that formed by the hetero-dimeric complex, CAD/ICAD. Comparison with other structural homologues revealed that the PB1 domain of BEM1P, ubiquitin-like domain of BAG6 and ubiquitin are structurally similar proteins. Our homo-dimeric structure of the CIDE-N domain of FSP27 will provide important information that will enable better understanding of the function of FSP27.

	Molecular basis for homo-dimerization of the CIDE domain revealed by the crystal structure of the CIDE-N domain of FSP27.,Lee SM, Jang TH, Park HH Biochem Biophys Res Commun. 2013 Oct 4;439(4):564-9. doi:, 10.1016/j.bbrc.2013.09.018. Epub 2013 Sep 8. PMID:24025675<ref>PMID:24025675</ref>

	~~From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>~~
	~~</div>~~
	~~<div class="pdbe-citations 4mac" style="background-color:#fffaf0;"></div>~~
	== References ==		== References ==
	<references/>		<references/>

OCA at 11:05, 21 December 2022

2022-12-21T11:05:56Z

← Older revision		Revision as of 11:05, 21 December 2022
Line 3:		Line 3:
	<StructureSection load='4mac' size='340' side='right'caption='[[4mac]], [[Resolution\|resolution]] 2.00Å' scene=''>		<StructureSection load='4mac' size='340' side='right'caption='[[4mac]], [[Resolution\|resolution]] 2.00Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Lk3_transgenic_mice Lk3 transgenic mice~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=4MAC FirstGlance]. <br>		<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4MAC FirstGlance]. <br>
	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">Cidec, Fsp27 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 LK3 transgenic mice])</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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [https://pdbe.org/4mac PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [https://www.ebi.ac.uk/pdbsum/4mac PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4mac 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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [~~http~~://pdbe.org/4mac PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/4mac PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=4mac ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
	[~~[http~~://www.uniprot.org/uniprot/CIDEC_MOUSE CIDEC_MOUSE]] Binds to lipid droplets and regulates their enlargement, thereby restricting lipolysis and favoring storage. At focal contact sites between lipid droplets, promotes directional net neutral lipid transfer from the smaller to larger lipid droplets. The transfer direction may be driven by the internal pressure difference between the contacting lipid droplet pair. Its role in neutral lipid transfer and lipid droplet enlargement is activated by the interaction with PLIN1. May act as a CEBPB coactivator in the white adipose tissue to control the expression of a subset of CEBPB downstream target genes, including SOCS1, SOCS3, TGFB1, TGFBR1, ID2 and XDH. When overexpressed in preadipocytes, induces apoptosis or increases cell susceptibility to apoptosis induced by serum deprivation or TGFB treatment. As mature adipocytes, that express high CIDEC levels, are quite resistant to apoptotic stimuli, the physiological significance of its role in apoptosis is unclear. May play a role in the modulation of the response to osmotic stress by preventing NFAT5 to translocate into the nucleus and activate its target genes expression.<ref>PMID:18334488</ref> <ref>PMID:22144693</ref> <ref>PMID:22245780</ref> <ref>PMID:23481402</ref>		[https://www.uniprot.org/uniprot/CIDEC_MOUSE CIDEC_MOUSE] Binds to lipid droplets and regulates their enlargement, thereby restricting lipolysis and favoring storage. At focal contact sites between lipid droplets, promotes directional net neutral lipid transfer from the smaller to larger lipid droplets. The transfer direction may be driven by the internal pressure difference between the contacting lipid droplet pair. Its role in neutral lipid transfer and lipid droplet enlargement is activated by the interaction with PLIN1. May act as a CEBPB coactivator in the white adipose tissue to control the expression of a subset of CEBPB downstream target genes, including SOCS1, SOCS3, TGFB1, TGFBR1, ID2 and XDH. When overexpressed in preadipocytes, induces apoptosis or increases cell susceptibility to apoptosis induced by serum deprivation or TGFB treatment. As mature adipocytes, that express high CIDEC levels, are quite resistant to apoptotic stimuli, the physiological significance of its role in apoptosis is unclear. May play a role in the modulation of the response to osmotic stress by preventing NFAT5 to translocate into the nucleus and activate its target genes expression.<ref>PMID:18334488</ref> <ref>PMID:22144693</ref> <ref>PMID:22245780</ref> <ref>PMID:23481402</ref>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 23:		Line 22:
	</StructureSection>		</StructureSection>
	[[Category: Large Structures]]		[[Category: Large Structures]]
	[[Category: ~~Lk3 transgenic mice~~]]		[[Category: Mus musculus]]
	[[Category: Lee~~, S M~~]]		[[Category: Lee SM]]
	[[Category: Park~~, H H]]~~		[[Category: Park HH]]
	~~[[Category: Apoptosis]]~~
	~~[[Category: Perilipin1]]~~
	~~[[Category: Protein interaction]]~~
	~~[[Category: Roll fold~~]]

OCA at 08:30, 3 April 2019

2019-04-03T08:30:57Z

← Older revision		Revision as of 08:30, 3 April 2019
Line 1:		Line 1:

	==Crystal structure of CIDE-N domain of FSP27==		==Crystal structure of CIDE-N domain of FSP27==
	<StructureSection load='4mac' size='340' side='right' caption='[[4mac]], [[Resolution\|resolution]] 2.00Å' scene=''>		<StructureSection load='4mac' size='340' side='right'caption='[[4mac]], [[Resolution\|resolution]] 2.00Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MAC FirstGlance]. <br>		<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MAC 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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [http://pdbe.org/4mac PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [http://www.ebi.ac.uk/pdbsum/4mac PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4mac ProSAT]</span></td></tr>		</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">Cidec, Fsp27 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 LK3 transgenic mice])</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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [http://pdbe.org/4mac PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [http://www.ebi.ac.uk/pdbsum/4mac PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4mac ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
Line 21:		Line 22:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
			[[Category: Large Structures]]
			[[Category: Lk3 transgenic mice]]
	[[Category: Lee, S M]]		[[Category: Lee, S M]]
	[[Category: Park, H H]]		[[Category: Park, H H]]

OCA at 17:56, 4 August 2016

2016-08-04T17:56:10Z

← Older revision		Revision as of 17:56, 4 August 2016
Line 1:		Line 1:

	==Crystal structure of CIDE-N domain of FSP27==		==Crystal structure of CIDE-N domain of FSP27==
	<StructureSection load='4mac' size='340' side='right' caption='[[4mac]], [[Resolution\|resolution]] 2.00Å' scene=''>		<StructureSection load='4mac' size='340' side='right' caption='[[4mac]], [[Resolution\|resolution]] 2.00Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MAC FirstGlance]. <br>		<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MAC 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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [http://www.ebi.ac.uk/pdbsum/4mac PDBsum]</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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [http://pdbe.org/4mac PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [http://www.ebi.ac.uk/pdbsum/4mac PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4mac ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
Line 15:		Line 16:
	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 4mac" style="background-color:#fffaf0;"></div>
	== References ==		== References ==
	<references/>		<references/>

OCA at 17:53, 24 December 2014

2014-12-24T17:53:59Z

← Older revision		Revision as of 17:53, 24 December 2014
Line 3:		Line 3:
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MAC FirstGlance]. <br>		<table><tr><td colspan='2'>[[4mac]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4MAC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4MAC FirstGlance]. <br>
	</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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [http://www.ebi.ac.uk/pdbsum/4mac PDBsum]</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=4mac FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4mac OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4mac RCSB], [http://www.ebi.ac.uk/pdbsum/4mac PDBsum]</span></td></tr>
	<table>		</table>
			== Function ==
			[[http://www.uniprot.org/uniprot/CIDEC_MOUSE CIDEC_MOUSE]] Binds to lipid droplets and regulates their enlargement, thereby restricting lipolysis and favoring storage. At focal contact sites between lipid droplets, promotes directional net neutral lipid transfer from the smaller to larger lipid droplets. The transfer direction may be driven by the internal pressure difference between the contacting lipid droplet pair. Its role in neutral lipid transfer and lipid droplet enlargement is activated by the interaction with PLIN1. May act as a CEBPB coactivator in the white adipose tissue to control the expression of a subset of CEBPB downstream target genes, including SOCS1, SOCS3, TGFB1, TGFBR1, ID2 and XDH. When overexpressed in preadipocytes, induces apoptosis or increases cell susceptibility to apoptosis induced by serum deprivation or TGFB treatment. As mature adipocytes, that express high CIDEC levels, are quite resistant to apoptotic stimuli, the physiological significance of its role in apoptosis is unclear. May play a role in the modulation of the response to osmotic stress by preventing NFAT5 to translocate into the nucleus and activate its target genes expression.<ref>PMID:18334488</ref> <ref>PMID:22144693</ref> <ref>PMID:22245780</ref> <ref>PMID:23481402</ref>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 17:		Line 19:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
	[[Category: Lee, S M.]]		[[Category: Lee, S M]]
	[[Category: Park, H H.]]		[[Category: Park, H H]]
	[[Category: Apoptosis]]		[[Category: Apoptosis]]
	[[Category: Perilipin1]]		[[Category: Perilipin1]]
	[[Category: Protein interaction]]		[[Category: Protein interaction]]
	[[Category: Roll fold]]		[[Category: Roll fold]]

OCA at 08:21, 2 July 2014

2014-07-02T08:21:15Z

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+==Crystal structure of CIDE-N domain of FSP27==
-The entry 4mac is ON HOLD  until Paper Publication
+Molecular basis for homo-dimerization of the CIDE domain revealed by the crystal structure of the CIDE-N domain of FSP27.,Lee SM, Jang TH, Park HH Biochem Biophys Res Commun. 2013 Oct 4;439(4):564-9. doi:, 10.1016/j.bbrc.2013.09.018. Epub 2013 Sep 8. PMID:24025675<ref>PMID:24025675</ref>
-Authors: Park, H.H., Lee, S.M.
+From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
+</div>
-Description: Crystal structure of CIDE-N domain of FSP27
+== References ==

OCA at 10:00, 4 September 2013

2013-09-04T10:00:21Z

← Older revision		Revision as of 10:00, 4 September 2013
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

	The entry 4mac is ON HOLD		The entry 4mac is ON HOLD until Paper Publication

	Authors: Park, H.H., Lee, S.M.		Authors: Park, H.H., Lee, S.M.

	Description: Crystal structure of CIDE-N domain of FSP27		Description: Crystal structure of CIDE-N domain of FSP27

OCA at 06:54, 28 August 2013

2013-08-28T06:54:43Z

← Older revision		Revision as of 06:54, 28 August 2013
Line 3:		Line 3:
	The entry 4mac is ON HOLD		The entry 4mac is ON HOLD

	Authors: Park, H.H, Lee, S.M		Authors: Park, H.H., Lee, S.M.

	Description: Crystal structure of CIDE-N domain of FSP27		Description: Crystal structure of CIDE-N domain of FSP27

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

2013-08-21T08:00:59Z

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

← Older revision	Revision as of 08:00, 21 August 2013
(No difference)

OCA: New page: '''Unreleased structure''' The entry 4mac is ON HOLD Authors: Park, H.H, Lee, S.M Description: Crystal structure of CIDE-N domain of FSP27

2013-08-21T08:00:58Z

New page: '''Unreleased structure''' The entry 4mac is ON HOLD Authors: Park, H.H, Lee, S.M Description: Crystal structure of CIDE-N domain of FSP27

New page

'''Unreleased structure'''

The entry 4mac is ON HOLD

Authors: Park, H.H, Lee, S.M

Description: Crystal structure of CIDE-N domain of FSP27