5jr8 - Revision history

OCA at 19:03, 20 September 2023

OCA — Wed, 20 Sep 2023 19:03:10 GMT

←Older revision		Revision as of 19:03, 20 September 2023
Line 3:		Line 3:
	<StructureSection load='5jr8' size='340' side='right'caption='[[5jr8]], [[Resolution\|resolution]] 2.65Å' scene=''>		<StructureSection load='5jr8' size='340' side='right'caption='[[5jr8]], [[Resolution\|resolution]] 2.65Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5jr8]] is a 2 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Human Human~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5JR8 OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://proteopedia.org/fgij/fg.htm?mol=5JR8 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5jr8]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5JR8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5JR8 FirstGlance]. <br>
-	</td></tr><tr id='~~ligand~~'><td class="sblockLbl"><b>[[~~Ligand~~\|~~Ligands~~:]]</b></td><td class="sblockDat" id="~~ligandDat~~">~~<scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>~~, ~~<scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</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]] 2.65Å</td></tr>
-	<tr id='~~gene~~'><td class="sblockLbl"><b>[[~~Gene~~\|~~Gene~~:]]</b></td><td class="sblockDat">~~LCN2, HNL, NGAL ([http~~:/~~/www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode~~=~~Info&srchmode~~=~~5&id=9606 HUMAN])~~</td></tr>	+	<tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</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=5jr8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jr8 OCA], [~~http~~://pdbe.org/5jr8 PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=5jr8 RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/5jr8 PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=5jr8 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=5jr8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jr8 OCA], [https://pdbe.org/5jr8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5jr8 RCSB], [https://www.ebi.ac.uk/pdbsum/5jr8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5jr8 ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
-	[~~[http~~://www.uniprot.org/uniprot/NGAL_HUMAN NGAL_HUMAN]] Iron-trafficking protein involved in multiple processes such as apoptosis, innate immunity and renal development. Binds iron through association with 2,5-dihydroxybenzoic acid (2,5-DHBA), a siderophore that shares structural similarities with bacterial enterobactin, and delivers or removes iron from the cell, depending on the context. Iron-bound form (holo-24p3) is internalized following binding to the SLC22A17 (24p3R) receptor, leading to release of iron and subsequent increase of intracellular iron concentration. In contrast, association of the iron-free form (apo-24p3) with the SLC22A17 (24p3R) receptor is followed by association with an intracellular siderophore, iron chelation and iron transfer to the extracellular medium, thereby reducing intracellular iron concentration. Involved in apoptosis due to interleukin-3 (IL3) deprivation: iron-loaded form increases intracellular iron concentration without promoting apoptosis, while iron-free form decreases intracellular iron levels, inducing expression of the proapoptotic protein BCL2L11/BIM, resulting in apoptosis. Involved in innate immunity, possibly by sequestrating iron, leading to limit bacterial growth.<ref>PMID:12453413</ref>	+	[https://www.uniprot.org/uniprot/NGAL_HUMAN NGAL_HUMAN] Iron-trafficking protein involved in multiple processes such as apoptosis, innate immunity and renal development. Binds iron through association with 2,5-dihydroxybenzoic acid (2,5-DHBA), a siderophore that shares structural similarities with bacterial enterobactin, and delivers or removes iron from the cell, depending on the context. Iron-bound form (holo-24p3) is internalized following binding to the SLC22A17 (24p3R) receptor, leading to release of iron and subsequent increase of intracellular iron concentration. In contrast, association of the iron-free form (apo-24p3) with the SLC22A17 (24p3R) receptor is followed by association with an intracellular siderophore, iron chelation and iron transfer to the extracellular medium, thereby reducing intracellular iron concentration. Involved in apoptosis due to interleukin-3 (IL3) deprivation: iron-loaded form increases intracellular iron concentration without promoting apoptosis, while iron-free form decreases intracellular iron levels, inducing expression of the proapoptotic protein BCL2L11/BIM, resulting in apoptosis. Involved in innate immunity, possibly by sequestrating iron, leading to limit bacterial growth.<ref>PMID:12453413</ref>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 22:		Line 22:
	==See Also==		==See Also==
	*[[Neutrophil gelatinase-associated lipocalin\|Neutrophil gelatinase-associated lipocalin]]		*[[Neutrophil gelatinase-associated lipocalin\|Neutrophil gelatinase-associated lipocalin]]
-	*[[Siderocalin\|Siderocalin]]	+	*[[Siderocalin 3D structures\|Siderocalin 3D structures]]
	== References ==		== References ==
	<references/>		<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: Abergel, R]]	+	[[Category: Abergel R]]
-	[[Category: Allred, B]]	+	[[Category: Allred B]]
-	[[Category: Barasch, J]]	+	[[Category: Barasch J]]
-	[[Category: Bruck, E]]	+	[[Category: Bruck E]]
-	[[Category: Buchen, C]]	+	[[Category: Buchen C]]
-	[[Category: Corbin, K]]	+	[[Category: Corbin K]]
-	[[Category: Darrah, S]]	+	[[Category: Darrah S]]
-	[[Category: Deng, R]]	+	[[Category: Deng R]]
-	[[Category: Graziano, J]]	+	[[Category: Graziano J]]
-	[[Category: Hod~~, E A~~]]	+	[[Category: Hod EA]]
-	[[Category: Hollman, M]]	+	[[Category: Hollman M]]
-	[[Category: Perlstein, A]]	+	[[Category: Perlstein A]]
-	[[Category: Qiu, A]]	+	[[Category: Qiu A]]
-	[[Category: Rupert~~, P B~~]]	+	[[Category: Rupert PB]]
-	[[Category: Slavkovich, V]]	+	[[Category: Slavkovich V]]
-	[[Category: Spitalnik, S]]	+	[[Category: Spitalnik S]]
-	[[Category: Stauber, J]]	+	[[Category: Stauber J]]
-	[[Category: Strong~~, R K~~]]	+	[[Category: Strong RK]]
-	[[Category: Tekabe, Y]]	+	[[Category: Tekabe Y]]
-	[[Category: Xu, K]]	+	[[Category: Xu K]]
-	~~[[Category: Fe-siderophore binding protein mutant]]~~	+
-	~~[[Category: Siderophore binding protein~~]]	+

OCA at 11:34, 17 June 2020

OCA — Wed, 17 Jun 2020 11:34:36 GMT

←Older revision		Revision as of 11:34, 17 June 2020
Line 1:		Line 1:

	==Disposal of Iron by a Mutant form of Siderocalin NGAL==		==Disposal of Iron by a Mutant form of Siderocalin NGAL==
-	<StructureSection load='5jr8' size='340' side='right' caption='[[5jr8]], [[Resolution\|resolution]] 2.65Å' scene=''>	+	<StructureSection load='5jr8' size='340' side='right'caption='[[5jr8]], [[Resolution\|resolution]] 2.65Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5jr8]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5JR8 OCA]. For a <b>guided tour on the structure components</b> use [http://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=5JR8 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5jr8]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5JR8 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=5JR8 FirstGlance]. <br>
-	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></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=5jr8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jr8 OCA], [http://pdbe.org/5jr8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5jr8 RCSB], [http://www.ebi.ac.uk/pdbsum/5jr8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5jr8 ProSAT]</span></td></tr>	+	<tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">LCN2, HNL, NGAL ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=5jr8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jr8 OCA], [http://pdbe.org/5jr8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5jr8 RCSB], [http://www.ebi.ac.uk/pdbsum/5jr8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5jr8 ProSAT]</span></td></tr>
	</table>		</table>
	== Function ==		== Function ==
Line 18:		Line 19:
	</div>		</div>
	<div class="pdbe-citations 5jr8" style="background-color:#fffaf0;"></div>		<div class="pdbe-citations 5jr8" style="background-color:#fffaf0;"></div>
		+
		+	==See Also==
		+	*[[Neutrophil gelatinase-associated lipocalin\|Neutrophil gelatinase-associated lipocalin]]
		+	*[[Siderocalin\|Siderocalin]]
	== References ==		== References ==
	<references/>		<references/>
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Abergel, R]]		[[Category: Abergel, R]]
	[[Category: Allred, B]]		[[Category: Allred, B]]

OCA at 03:38, 10 December 2016

OCA — Sat, 10 Dec 2016 03:38:08 GMT

←Older revision		Revision as of 03:38, 10 December 2016
Line 9:		Line 9:
	== Function ==		== Function ==
	[[http://www.uniprot.org/uniprot/NGAL_HUMAN NGAL_HUMAN]] Iron-trafficking protein involved in multiple processes such as apoptosis, innate immunity and renal development. Binds iron through association with 2,5-dihydroxybenzoic acid (2,5-DHBA), a siderophore that shares structural similarities with bacterial enterobactin, and delivers or removes iron from the cell, depending on the context. Iron-bound form (holo-24p3) is internalized following binding to the SLC22A17 (24p3R) receptor, leading to release of iron and subsequent increase of intracellular iron concentration. In contrast, association of the iron-free form (apo-24p3) with the SLC22A17 (24p3R) receptor is followed by association with an intracellular siderophore, iron chelation and iron transfer to the extracellular medium, thereby reducing intracellular iron concentration. Involved in apoptosis due to interleukin-3 (IL3) deprivation: iron-loaded form increases intracellular iron concentration without promoting apoptosis, while iron-free form decreases intracellular iron levels, inducing expression of the proapoptotic protein BCL2L11/BIM, resulting in apoptosis. Involved in innate immunity, possibly by sequestrating iron, leading to limit bacterial growth.<ref>PMID:12453413</ref>		[[http://www.uniprot.org/uniprot/NGAL_HUMAN NGAL_HUMAN]] Iron-trafficking protein involved in multiple processes such as apoptosis, innate immunity and renal development. Binds iron through association with 2,5-dihydroxybenzoic acid (2,5-DHBA), a siderophore that shares structural similarities with bacterial enterobactin, and delivers or removes iron from the cell, depending on the context. Iron-bound form (holo-24p3) is internalized following binding to the SLC22A17 (24p3R) receptor, leading to release of iron and subsequent increase of intracellular iron concentration. In contrast, association of the iron-free form (apo-24p3) with the SLC22A17 (24p3R) receptor is followed by association with an intracellular siderophore, iron chelation and iron transfer to the extracellular medium, thereby reducing intracellular iron concentration. Involved in apoptosis due to interleukin-3 (IL3) deprivation: iron-loaded form increases intracellular iron concentration without promoting apoptosis, while iron-free form decreases intracellular iron levels, inducing expression of the proapoptotic protein BCL2L11/BIM, resulting in apoptosis. Involved in innate immunity, possibly by sequestrating iron, leading to limit bacterial growth.<ref>PMID:12453413</ref>
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Iron overload damages many organs. Unfortunately, therapeutic iron chelators also have undesired toxicity and may deliver iron to microbes. Here we show that a mutant form (K3Cys) of endogenous lipocalin 2 (LCN2) is filtered by the kidney but can bypass sites of megalin-dependent recapture, resulting in urinary excretion. Because K3Cys maintains recognition of its cognate ligand, the iron siderophore enterochelin, this protein can capture and transport iron even in the acidic conditions of urine. Mutant LCN2 strips iron from transferrin and citrate, and delivers it into the urine. In addition, it removes iron from iron overloaded mice, including models of acquired (iron-dextran or stored red blood cells) and primary (Hfe-/-) iron overload. In each case, the mutants reduce redox activity typical of non-transferrin-bound iron. In summary, we present a non-toxic strategy for iron chelation and urinary elimination, based on manipulating an endogenous protein:siderophore:iron clearance pathway.
		+
		+	Disposal of iron by a mutant form of lipocalin 2.,Barasch J, Hollmen M, Deng R, Hod EA, Rupert PB, Abergel RJ, Allred BE, Xu K, Darrah SF, Tekabe Y, Perlstein A, Wax R, Bruck E, Stauber J, Corbin KA, Buchen C, Slavkovich V, Graziano J, Spitalnik SL, Bao G, Strong RK, Qiu A Nat Commun. 2016 Oct 31;7:12973. doi: 10.1038/ncomms12973. PMID:27796299<ref>PMID:27796299</ref>
		+
		+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>
		+	<div class="pdbe-citations 5jr8" style="background-color:#fffaf0;"></div>
	== References ==		== References ==
	<references/>		<references/>

OCA at 17:09, 3 October 2016

OCA — Mon, 03 Oct 2016 17:09:04 GMT

←Older revision		Revision as of 17:09, 3 October 2016
Line 1:		Line 1:
-	'''Unreleased structure'''

-	~~The entry~~ 5jr8 ~~is ON HOLD until Paper Publication~~	+	==Disposal of Iron by a Mutant form of Siderocalin NGAL==
-		+	<StructureSection load='5jr8' size='340' side='right' caption='[[5jr8]], [[Resolution\|resolution]] 2.65Å' scene=''>
-	~~Authors~~: ~~Rupert, P~~.B.~~, Strong, R~~.K.~~, Barasch, J~~.~~, Hollman, M~~.~~, Deng, R~~.~~, Hod, E~~.A., ~~Abergel, R~~.~~, Allred, B~~., ~~Xu, K~~., ~~Darrah, S~~., ~~Tekabe, Y~~., ~~Perlstein, A~~., ~~Bruck, E~~., ~~Stauber, J~~., ~~Corbin~~, K., ~~Buchen~~, C., ~~Slavkovich~~, V., ~~Graziano~~, J., ~~Spitalnik~~, S., ~~Qiu~~, A.	+	== Structural highlights ==
-		+	<table><tr><td colspan='2'>[[5jr8]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5JR8 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5JR8 FirstGlance]. <br>
-	~~Description: Disposal of Iron by a Mutant form of Siderocalin NGAL~~	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>
-	~~[[Category: Unreleased Structures]]~~	+	<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=5jr8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jr8 OCA], [http://pdbe.org/5jr8 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5jr8 RCSB], [http://www.ebi.ac.uk/pdbsum/5jr8 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5jr8 ProSAT]</span></td></tr>
-	[[Category: ~~Tekabe~~, Y]]	+	</table>
		+	== Function ==
		+	[[http://www.uniprot.org/uniprot/NGAL_HUMAN NGAL_HUMAN]] Iron-trafficking protein involved in multiple processes such as apoptosis, innate immunity and renal development. Binds iron through association with 2,5-dihydroxybenzoic acid (2,5-DHBA), a siderophore that shares structural similarities with bacterial enterobactin, and delivers or removes iron from the cell, depending on the context. Iron-bound form (holo-24p3) is internalized following binding to the SLC22A17 (24p3R) receptor, leading to release of iron and subsequent increase of intracellular iron concentration. In contrast, association of the iron-free form (apo-24p3) with the SLC22A17 (24p3R) receptor is followed by association with an intracellular siderophore, iron chelation and iron transfer to the extracellular medium, thereby reducing intracellular iron concentration. Involved in apoptosis due to interleukin-3 (IL3) deprivation: iron-loaded form increases intracellular iron concentration without promoting apoptosis, while iron-free form decreases intracellular iron levels, inducing expression of the proapoptotic protein BCL2L11/BIM, resulting in apoptosis. Involved in innate immunity, possibly by sequestrating iron, leading to limit bacterial growth.<ref>PMID:12453413</ref>
		+	== References ==
		+	<references/>
		+	__TOC__
		+	</StructureSection>
		+	[[Category: Abergel, R]]
	[[Category: Allred, B]]		[[Category: Allred, B]]
-	[[Category: Hod, E.A]]
-	[[Category: Graziano, J]]
-	[[Category: Spitalnik, S]]
-	[[Category: Deng, R]]
-	[[Category: Strong, R.K]]
-	[[Category: Xu, K]]
-	[[Category: Darrah, S]]
	[[Category: Barasch, J]]		[[Category: Barasch, J]]
-	[[Category: ~~Abergel~~, R]]	+	[[Category: Bruck, E]]
-	[[Category: ~~Slavkovich~~, ~~V]]~~	+	[[Category: Buchen, C]]
-	~~[[Category: Stauber, J~~]]	+
	[[Category: Corbin, K]]		[[Category: Corbin, K]]
-	[[Category: ~~Rupert~~, ~~P.B~~]]	+	[[Category: Darrah, S]]
		+	[[Category: Deng, R]]
		+	[[Category: Graziano, J]]
		+	[[Category: Hod, E A]]
		+	[[Category: Hollman, M]]
	[[Category: Perlstein, A]]		[[Category: Perlstein, A]]
-	[[Category: Hollman, M]]
-	[[Category: Bruck, E]]
-	[[Category: Buchen, C]]
	[[Category: Qiu, A]]		[[Category: Qiu, A]]
		+	[[Category: Rupert, P B]]
		+	[[Category: Slavkovich, V]]
		+	[[Category: Spitalnik, S]]
		+	[[Category: Stauber, J]]
		+	[[Category: Strong, R K]]
		+	[[Category: Tekabe, Y]]
		+	[[Category: Xu, K]]
		+	[[Category: Fe-siderophore binding protein mutant]]
		+	[[Category: Siderophore binding protein]]

OCA at 13:43, 1 June 2016

OCA — Wed, 01 Jun 2016 13:43:28 GMT

←Older revision		Revision as of 13:43, 1 June 2016
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 5jr8 is ON HOLD	+	The entry 5jr8 is ON HOLD until Paper Publication

	Authors: Rupert, P.B., Strong, R.K., Barasch, J., Hollman, M., Deng, R., Hod, E.A., Abergel, R., Allred, B., Xu, K., Darrah, S., Tekabe, Y., Perlstein, A., Bruck, E., Stauber, J., Corbin, K., Buchen, C., Slavkovich, V., Graziano, J., Spitalnik, S., Qiu, A.		Authors: Rupert, P.B., Strong, R.K., Barasch, J., Hollman, M., Deng, R., Hod, E.A., Abergel, R., Allred, B., Xu, K., Darrah, S., Tekabe, Y., Perlstein, A., Bruck, E., Stauber, J., Corbin, K., Buchen, C., Slavkovich, V., Graziano, J., Spitalnik, S., Qiu, A.

OCA: Protected "5jr8" [edit=sysop:move=sysop]

OCA — Sun, 15 May 2016 15:47:56 GMT

Protected "5jr8" [edit=sysop:move=sysop]

←Older revision

Revision as of 15:47, 15 May 2016

OCA: New page: '''Unreleased structure''' The entry 5jr8 is ON HOLD Authors: Rupert, P.B., Strong, R.K., Barasch, J., Hollman, M., Deng, R., Hod, E.A., Abergel, R., Allred, B., Xu, K., Darrah, S., Tek...

OCA — Sun, 15 May 2016 15:47:54 GMT

New page: '''Unreleased structure''' The entry 5jr8 is ON HOLD Authors: Rupert, P.B., Strong, R.K., Barasch, J., Hollman, M., Deng, R., Hod, E.A., Abergel, R., Allred, B., Xu, K., Darrah, S., Tek...

New page

'''Unreleased structure'''

The entry 5jr8 is ON HOLD

Authors: Rupert, P.B., Strong, R.K., Barasch, J., Hollman, M., Deng, R., Hod, E.A., Abergel, R., Allred, B., Xu, K., Darrah, S., Tekabe, Y., Perlstein, A., Bruck, E., Stauber, J., Corbin, K., Buchen, C., Slavkovich, V., Graziano, J., Spitalnik, S., Qiu, A.

Description: Disposal of Iron by a Mutant form of Siderocalin NGAL
[[Category: Unreleased Structures]]
[[Category: Tekabe, Y]]
[[Category: Allred, B]]
[[Category: Hod, E.A]]
[[Category: Graziano, J]]
[[Category: Spitalnik, S]]
[[Category: Deng, R]]
[[Category: Strong, R.K]]
[[Category: Xu, K]]
[[Category: Darrah, S]]
[[Category: Barasch, J]]
[[Category: Abergel, R]]
[[Category: Slavkovich, V]]
[[Category: Stauber, J]]
[[Category: Corbin, K]]
[[Category: Rupert, P.B]]
[[Category: Perlstein, A]]
[[Category: Hollman, M]]
[[Category: Bruck, E]]
[[Category: Buchen, C]]
[[Category: Qiu, A]]