4bcz - Revision history

OCA at 11:48, 20 December 2023

OCA — Wed, 20 Dec 2023 11:48:10 GMT

←Older revision		Revision as of 11:48, 20 December 2023
Line 3:		Line 3:
	<StructureSection load='4bcz' size='340' side='right'caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>		<StructureSection load='4bcz' size='340' side='right'caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[4bcz]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/~~Human Human~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BCZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4BCZ FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[4bcz]] 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=4BCZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4BCZ FirstGlance]. <br>
-	</td></tr><tr id='~~related~~'><td class="sblockLbl"><b>[[~~Related_structure~~\|~~Related~~:]]</b></td><td class="sblockDat">~~<div style='overflow: auto; max~~-~~height: 3em;'>[[1azv\|1azv]]~~, [[~~1ba9~~\|~~1ba9~~]], [[1dsw\|1dsw]], [[1fun\|1fun]], [[1hl4\|1hl4]], [[1hl5\|1hl5]], [[1kmg\|1kmg]], [[1l3n\|1l3n]], [[1mfm\|1mfm]], [[1n18\|1n18]], [[1n19\|1n19]], [[1oez\|1oez]], [[1ozt\|1ozt]], [[1ozu\|1ozu]], [[1p1v\|1p1v]], [[1ptz\|1ptz]], [[1pu0\|1pu0]], [[1rk7\|1rk7]], [[1sos\|1sos]], [[1spd\|1spd]], [[1uxl\|1uxl]], [[1uxm\|1uxm]], [[2af2\|2af2]], [[2c9s\|2c9s]], [[2c9u\|2c9u]], [[2c9v\|2c9v]], [[2v0a\|2v0a]], [[2vr6\|2vr6]], [[2vr7\|2vr7]], [[2vr8\|2vr8]], [[2wko\|2wko]], [[2wyt\|2wyt]], [[2wyz\|2wyz]], [[2wz0\|2wz0]], [[2wz5\|2wz5]], [[2wz6\|2wz6]], [[2xjk\|2xjk]], [[2xjl\|2xjl]], [[4a7g\|4a7g]], [[4a7q\|4a7q]], [[4a7r\|4a7r]], [[4a7s\|4a7s]], [[4a7t\|4a7t]], [[4a7u\|4a7u]], [[4a7v\|4a7v]], [[4b3e\|4b3e]], [[4bcy\|4bcy]]</div></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]] 1.93Å</td></tr>
-	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.~~15.1.1 1.15.1.1] </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=4bcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bcz OCA], [https://pdbe.org/4bcz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4bcz RCSB], [https://www.ebi.ac.uk/pdbsum/4bcz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4bcz 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=4bcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bcz OCA], [https://pdbe.org/4bcz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4bcz RCSB], [https://www.ebi.ac.uk/pdbsum/4bcz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4bcz ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
-	[[https://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Defects in SOD1 are the cause of amyotrophic lateral sclerosis type 1 (ALS1) [MIM:[https://omim.org/entry/105400 105400]]. ALS1 is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of cases leading to familial forms.<ref>PMID:12963370</ref> <ref>PMID:19741096</ref> <ref>PMID:8528216</ref> <ref>PMID:8682505</ref> <ref>PMID:9541385</ref> <ref>PMID:12754496</ref> <ref>PMID:15056757</ref> <ref>PMID:18378676</ref> [:]<ref>PMID:8446170</ref> <ref>PMID:8351519</ref> <ref>PMID:8179602</ref> <ref>PMID:7980516</ref> <ref>PMID:8069312</ref> <ref>PMID:7951252</ref> <ref>PMID:7881433</ref> <ref>PMID:7836951</ref> <ref>PMID:7997024</ref> <ref>PMID:7870076</ref> <ref>PMID:7887412</ref> <ref>PMID:7795609</ref> <ref>PMID:7655468</ref> <ref>PMID:7655469</ref> <ref>PMID:7655471</ref> <ref>PMID:7700376</ref> <ref>PMID:7647793</ref> <ref>PMID:7501156</ref> <ref>PMID:7496169</ref> <ref>PMID:8938700</ref> <ref>PMID:8907321</ref> <ref>PMID:8990014</ref> <ref>PMID:9101297</ref> <ref>PMID:9455977</ref> <ref>PMID:10732812</ref> <ref>PMID:9131652</ref> <ref>PMID:10400992</ref> <ref>PMID:10430435</ref> <ref>PMID:11535232</ref> <ref>PMID:11369193</ref> <ref>PMID:12402272</ref> <ref>PMID:12145308</ref> <ref>PMID:14506936</ref> <ref>PMID:18552350</ref> <ref>PMID:18301754</ref> <ref>PMID:21247266</ref> <ref>PMID:21220647</ref>	+	[https://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN] Defects in SOD1 are the cause of amyotrophic lateral sclerosis type 1 (ALS1) [MIM:[https://omim.org/entry/105400 105400]. ALS1 is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of cases leading to familial forms.<ref>PMID:12963370</ref> <ref>PMID:19741096</ref> <ref>PMID:8528216</ref> <ref>PMID:8682505</ref> <ref>PMID:9541385</ref> <ref>PMID:12754496</ref> <ref>PMID:15056757</ref> <ref>PMID:18378676</ref> [:]<ref>PMID:8446170</ref> <ref>PMID:8351519</ref> <ref>PMID:8179602</ref> <ref>PMID:7980516</ref> <ref>PMID:8069312</ref> <ref>PMID:7951252</ref> <ref>PMID:7881433</ref> <ref>PMID:7836951</ref> <ref>PMID:7997024</ref> <ref>PMID:7870076</ref> <ref>PMID:7887412</ref> <ref>PMID:7795609</ref> <ref>PMID:7655468</ref> <ref>PMID:7655469</ref> <ref>PMID:7655471</ref> <ref>PMID:7700376</ref> <ref>PMID:7647793</ref> <ref>PMID:7501156</ref> <ref>PMID:7496169</ref> <ref>PMID:8938700</ref> <ref>PMID:8907321</ref> <ref>PMID:8990014</ref> <ref>PMID:9101297</ref> <ref>PMID:9455977</ref> <ref>PMID:10732812</ref> <ref>PMID:9131652</ref> <ref>PMID:10400992</ref> <ref>PMID:10430435</ref> <ref>PMID:11535232</ref> <ref>PMID:11369193</ref> <ref>PMID:12402272</ref> <ref>PMID:12145308</ref> <ref>PMID:14506936</ref> <ref>PMID:18552350</ref> <ref>PMID:18301754</ref> <ref>PMID:21247266</ref> <ref>PMID:21220647</ref>
	== Function ==		== Function ==
-	[[https://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Destroys radicals which are normally produced within the cells and which are toxic to biological systems.	+	[https://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN] Destroys radicals which are normally produced within the cells and which are toxic to biological systems.
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
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	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	~~[[Category: Superoxide dismutase]]~~	+	[[Category: Awad W]]
-	[[Category: Awad, W]]	+	[[Category: Danielsson J]]
-	[[Category: Danielsson, J]]	+	[[Category: Kurnik M]]
-	[[Category: Kurnik, M]]	+	[[Category: Lang L]]
-	[[Category: Lang, L]]	+	[[Category: Logan DT]]
-	[[Category: Logan~~, D T~~]]	+	[[Category: Marklund SL]]
-	[[Category: Marklund~~, S L~~]]	+	[[Category: Oliveberg M]]
-	[[Category: Oliveberg, M]]	+	[[Category: Saraboji K]]
-	[[Category: Saraboji, K]]	+
-	~~[[Category: Al]]~~	+
-	~~[[Category: Cu/zn sod1]]~~	+
-	~~[[Category: Disease mutation]]~~	+
-	~~[[Category: Metal binding]]~~	+
-	~~[[Category: Monomeric mutant]]~~	+
-	~~[[Category: Neurodegeneration]]~~	+
-	~~[[Category: Oxidoreductase~~]]	+

OCA at 07:08, 31 August 2022

OCA — Wed, 31 Aug 2022 07:08:41 GMT

←Older revision		Revision as of 07:08, 31 August 2022
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	<StructureSection load='4bcz' size='340' side='right'caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>		<StructureSection load='4bcz' size='340' side='right'caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[4bcz]] 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=4BCZ OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=4BCZ FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[4bcz]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BCZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4BCZ FirstGlance]. <br>
-	</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[1azv\|1azv]], [[1ba9\|1ba9]], [[1dsw\|1dsw]], [[1fun\|1fun]], [[1hl4\|1hl4]], [[1hl5\|1hl5]], [[1kmg\|1kmg]], [[1l3n\|1l3n]], [[1mfm\|1mfm]], [[1n18\|1n18]], [[1n19\|1n19]], [[1oez\|1oez]], [[1ozt\|1ozt]], [[1ozu\|1ozu]], [[1p1v\|1p1v]], [[1ptz\|1ptz]], [[1pu0\|1pu0]], [[1rk7\|1rk7]], [[1sos\|1sos]], [[1spd\|1spd]], [[1uxl\|1uxl]], [[1uxm\|1uxm]], [[2af2\|2af2]], [[2c9s\|2c9s]], [[2c9u\|2c9u]], [[2c9v\|2c9v]], [[2v0a\|2v0a]], [[2vr6\|2vr6]], [[2vr7\|2vr7]], [[2vr8\|2vr8]], [[2wko\|2wko]], [[2wyt\|2wyt]], [[2wyz\|2wyz]], [[2wz0\|2wz0]], [[2wz5\|2wz5]], [[2wz6\|2wz6]], [[2xjk\|2xjk]], [[2xjl\|2xjl]], [[4a7g\|4a7g]], [[4a7q\|4a7q]], [[4a7r\|4a7r]], [[4a7s\|4a7s]], [[4a7t\|4a7t]], [[4a7u\|4a7u]], [[4a7v\|4a7v]], [[4b3e\|4b3e]], [[4bcy\|4bcy]]</td></tr>	+	</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1azv\|1azv]], [[1ba9\|1ba9]], [[1dsw\|1dsw]], [[1fun\|1fun]], [[1hl4\|1hl4]], [[1hl5\|1hl5]], [[1kmg\|1kmg]], [[1l3n\|1l3n]], [[1mfm\|1mfm]], [[1n18\|1n18]], [[1n19\|1n19]], [[1oez\|1oez]], [[1ozt\|1ozt]], [[1ozu\|1ozu]], [[1p1v\|1p1v]], [[1ptz\|1ptz]], [[1pu0\|1pu0]], [[1rk7\|1rk7]], [[1sos\|1sos]], [[1spd\|1spd]], [[1uxl\|1uxl]], [[1uxm\|1uxm]], [[2af2\|2af2]], [[2c9s\|2c9s]], [[2c9u\|2c9u]], [[2c9v\|2c9v]], [[2v0a\|2v0a]], [[2vr6\|2vr6]], [[2vr7\|2vr7]], [[2vr8\|2vr8]], [[2wko\|2wko]], [[2wyt\|2wyt]], [[2wyz\|2wyz]], [[2wz0\|2wz0]], [[2wz5\|2wz5]], [[2wz6\|2wz6]], [[2xjk\|2xjk]], [[2xjl\|2xjl]], [[4a7g\|4a7g]], [[4a7q\|4a7q]], [[4a7r\|4a7r]], [[4a7s\|4a7s]], [[4a7t\|4a7t]], [[4a7u\|4a7u]], [[4a7v\|4a7v]], [[4b3e\|4b3e]], [[4bcy\|4bcy]]</div></td></tr>
-	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[~~http~~://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [~~http~~://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.1 1.15.1.1] </span></td></tr>	+	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.1 1.15.1.1] </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=4bcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bcz OCA], [~~http~~://pdbe.org/4bcz PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=4bcz RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/4bcz PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=4bcz 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=4bcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bcz OCA], [https://pdbe.org/4bcz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4bcz RCSB], [https://www.ebi.ac.uk/pdbsum/4bcz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4bcz ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
-	[[~~http~~://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Defects in SOD1 are the cause of amyotrophic lateral sclerosis type 1 (ALS1) [MIM:[~~http~~://omim.org/entry/105400 105400]]. ALS1 is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of cases leading to familial forms.<ref>PMID:12963370</ref> <ref>PMID:19741096</ref> <ref>PMID:8528216</ref> <ref>PMID:8682505</ref> <ref>PMID:9541385</ref> <ref>PMID:12754496</ref> <ref>PMID:15056757</ref> <ref>PMID:18378676</ref> [:]<ref>PMID:8446170</ref> <ref>PMID:8351519</ref> <ref>PMID:8179602</ref> <ref>PMID:7980516</ref> <ref>PMID:8069312</ref> <ref>PMID:7951252</ref> <ref>PMID:7881433</ref> <ref>PMID:7836951</ref> <ref>PMID:7997024</ref> <ref>PMID:7870076</ref> <ref>PMID:7887412</ref> <ref>PMID:7795609</ref> <ref>PMID:7655468</ref> <ref>PMID:7655469</ref> <ref>PMID:7655471</ref> <ref>PMID:7700376</ref> <ref>PMID:7647793</ref> <ref>PMID:7501156</ref> <ref>PMID:7496169</ref> <ref>PMID:8938700</ref> <ref>PMID:8907321</ref> <ref>PMID:8990014</ref> <ref>PMID:9101297</ref> <ref>PMID:9455977</ref> <ref>PMID:10732812</ref> <ref>PMID:9131652</ref> <ref>PMID:10400992</ref> <ref>PMID:10430435</ref> <ref>PMID:11535232</ref> <ref>PMID:11369193</ref> <ref>PMID:12402272</ref> <ref>PMID:12145308</ref> <ref>PMID:14506936</ref> <ref>PMID:18552350</ref> <ref>PMID:18301754</ref> <ref>PMID:21247266</ref> <ref>PMID:21220647</ref>	+	[[https://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Defects in SOD1 are the cause of amyotrophic lateral sclerosis type 1 (ALS1) [MIM:[https://omim.org/entry/105400 105400]]. ALS1 is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of cases leading to familial forms.<ref>PMID:12963370</ref> <ref>PMID:19741096</ref> <ref>PMID:8528216</ref> <ref>PMID:8682505</ref> <ref>PMID:9541385</ref> <ref>PMID:12754496</ref> <ref>PMID:15056757</ref> <ref>PMID:18378676</ref> [:]<ref>PMID:8446170</ref> <ref>PMID:8351519</ref> <ref>PMID:8179602</ref> <ref>PMID:7980516</ref> <ref>PMID:8069312</ref> <ref>PMID:7951252</ref> <ref>PMID:7881433</ref> <ref>PMID:7836951</ref> <ref>PMID:7997024</ref> <ref>PMID:7870076</ref> <ref>PMID:7887412</ref> <ref>PMID:7795609</ref> <ref>PMID:7655468</ref> <ref>PMID:7655469</ref> <ref>PMID:7655471</ref> <ref>PMID:7700376</ref> <ref>PMID:7647793</ref> <ref>PMID:7501156</ref> <ref>PMID:7496169</ref> <ref>PMID:8938700</ref> <ref>PMID:8907321</ref> <ref>PMID:8990014</ref> <ref>PMID:9101297</ref> <ref>PMID:9455977</ref> <ref>PMID:10732812</ref> <ref>PMID:9131652</ref> <ref>PMID:10400992</ref> <ref>PMID:10430435</ref> <ref>PMID:11535232</ref> <ref>PMID:11369193</ref> <ref>PMID:12402272</ref> <ref>PMID:12145308</ref> <ref>PMID:14506936</ref> <ref>PMID:18552350</ref> <ref>PMID:18301754</ref> <ref>PMID:21247266</ref> <ref>PMID:21220647</ref>
	== Function ==		== Function ==
-	[[~~http~~://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Destroys radicals which are normally produced within the cells and which are toxic to biological systems.	+	[[https://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Destroys radicals which are normally produced within the cells and which are toxic to biological systems.
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 23:		Line 23:

	==See Also==		==See Also==
-	*[[Superoxide ~~Dismutase~~\|Superoxide ~~Dismutase~~]]	+	*[[Superoxide dismutase 3D structures\|Superoxide dismutase 3D structures]]
	== References ==		== References ==
	<references/>		<references/>

OCA at 12:42, 10 May 2019

OCA — Fri, 10 May 2019 12:42:24 GMT

←Older revision		Revision as of 12:42, 10 May 2019
Line 1:		Line 1:

	==Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.==		==Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.==
-	<StructureSection load='4bcz' size='340' side='right' caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>	+	<StructureSection load='4bcz' size='340' side='right'caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4bcz]] 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=4BCZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4BCZ FirstGlance]. <br>		<table><tr><td colspan='2'>[[4bcz]] 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=4BCZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4BCZ FirstGlance]. <br>
Line 21:		Line 21:
	</div>		</div>
	<div class="pdbe-citations 4bcz" style="background-color:#fffaf0;"></div>		<div class="pdbe-citations 4bcz" style="background-color:#fffaf0;"></div>
		+
		+	==See Also==
		+	*[[Superoxide Dismutase\|Superoxide Dismutase]]
	== References ==		== References ==
	<references/>		<references/>
Line 26:		Line 29:
	</StructureSection>		</StructureSection>
	[[Category: Human]]		[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Superoxide dismutase]]		[[Category: Superoxide dismutase]]
	[[Category: Awad, W]]		[[Category: Awad, W]]

OCA at 07:43, 17 January 2018

OCA — Wed, 17 Jan 2018 07:43:57 GMT

←Older revision		Revision as of 07:43, 17 January 2018
Line 21:		Line 21:
	</div>		</div>
	<div class="pdbe-citations 4bcz" style="background-color:#fffaf0;"></div>		<div class="pdbe-citations 4bcz" style="background-color:#fffaf0;"></div>
-
-	==See Also==
-	*[[Superoxide Dismutase\|Superoxide Dismutase]]
	== References ==		== References ==
	<references/>		<references/>

OCA at 12:43, 11 August 2016

OCA — Thu, 11 Aug 2016 12:43:08 GMT

←Older revision		Revision as of 12:43, 11 August 2016
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		+
	==Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.==		==Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.==
	<StructureSection load='4bcz' size='340' side='right' caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>		<StructureSection load='4bcz' size='340' side='right' caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>
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	</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[1azv\|1azv]], [[1ba9\|1ba9]], [[1dsw\|1dsw]], [[1fun\|1fun]], [[1hl4\|1hl4]], [[1hl5\|1hl5]], [[1kmg\|1kmg]], [[1l3n\|1l3n]], [[1mfm\|1mfm]], [[1n18\|1n18]], [[1n19\|1n19]], [[1oez\|1oez]], [[1ozt\|1ozt]], [[1ozu\|1ozu]], [[1p1v\|1p1v]], [[1ptz\|1ptz]], [[1pu0\|1pu0]], [[1rk7\|1rk7]], [[1sos\|1sos]], [[1spd\|1spd]], [[1uxl\|1uxl]], [[1uxm\|1uxm]], [[2af2\|2af2]], [[2c9s\|2c9s]], [[2c9u\|2c9u]], [[2c9v\|2c9v]], [[2v0a\|2v0a]], [[2vr6\|2vr6]], [[2vr7\|2vr7]], [[2vr8\|2vr8]], [[2wko\|2wko]], [[2wyt\|2wyt]], [[2wyz\|2wyz]], [[2wz0\|2wz0]], [[2wz5\|2wz5]], [[2wz6\|2wz6]], [[2xjk\|2xjk]], [[2xjl\|2xjl]], [[4a7g\|4a7g]], [[4a7q\|4a7q]], [[4a7r\|4a7r]], [[4a7s\|4a7s]], [[4a7t\|4a7t]], [[4a7u\|4a7u]], [[4a7v\|4a7v]], [[4b3e\|4b3e]], [[4bcy\|4bcy]]</td></tr>		</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[1azv\|1azv]], [[1ba9\|1ba9]], [[1dsw\|1dsw]], [[1fun\|1fun]], [[1hl4\|1hl4]], [[1hl5\|1hl5]], [[1kmg\|1kmg]], [[1l3n\|1l3n]], [[1mfm\|1mfm]], [[1n18\|1n18]], [[1n19\|1n19]], [[1oez\|1oez]], [[1ozt\|1ozt]], [[1ozu\|1ozu]], [[1p1v\|1p1v]], [[1ptz\|1ptz]], [[1pu0\|1pu0]], [[1rk7\|1rk7]], [[1sos\|1sos]], [[1spd\|1spd]], [[1uxl\|1uxl]], [[1uxm\|1uxm]], [[2af2\|2af2]], [[2c9s\|2c9s]], [[2c9u\|2c9u]], [[2c9v\|2c9v]], [[2v0a\|2v0a]], [[2vr6\|2vr6]], [[2vr7\|2vr7]], [[2vr8\|2vr8]], [[2wko\|2wko]], [[2wyt\|2wyt]], [[2wyz\|2wyz]], [[2wz0\|2wz0]], [[2wz5\|2wz5]], [[2wz6\|2wz6]], [[2xjk\|2xjk]], [[2xjl\|2xjl]], [[4a7g\|4a7g]], [[4a7q\|4a7q]], [[4a7r\|4a7r]], [[4a7s\|4a7s]], [[4a7t\|4a7t]], [[4a7u\|4a7u]], [[4a7v\|4a7v]], [[4b3e\|4b3e]], [[4bcy\|4bcy]]</td></tr>
	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.1 1.15.1.1] </span></td></tr>		<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.1 1.15.1.1] </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=4bcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bcz OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4bcz RCSB], [http://www.ebi.ac.uk/pdbsum/4bcz 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=4bcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bcz OCA], [http://pdbe.org/4bcz PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4bcz RCSB], [http://www.ebi.ac.uk/pdbsum/4bcz PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4bcz ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
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	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 4bcz" style="background-color:#fffaf0;"></div>

	==See Also==		==See Also==

OCA at 12:44, 4 January 2015

OCA — Sun, 04 Jan 2015 12:44:04 GMT

←Older revision		Revision as of 12:44, 4 January 2015
Line 1:		Line 1:
-	[[~~Image:~~4bcz.~~jpg~~\|~~left~~\|~~200px~~]]	+	==Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.==
		+	<StructureSection load='4bcz' size='340' side='right' caption='[[4bcz]], [[Resolution\|resolution]] 1.93Å' scene=''>
		+	== Structural highlights ==
		+	<table><tr><td colspan='2'>[[4bcz]] 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=4BCZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4BCZ FirstGlance]. <br>
		+	</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[1azv\|1azv]], [[1ba9\|1ba9]], [[1dsw\|1dsw]], [[1fun\|1fun]], [[1hl4\|1hl4]], [[1hl5\|1hl5]], [[1kmg\|1kmg]], [[1l3n\|1l3n]], [[1mfm\|1mfm]], [[1n18\|1n18]], [[1n19\|1n19]], [[1oez\|1oez]], [[1ozt\|1ozt]], [[1ozu\|1ozu]], [[1p1v\|1p1v]], [[1ptz\|1ptz]], [[1pu0\|1pu0]], [[1rk7\|1rk7]], [[1sos\|1sos]], [[1spd\|1spd]], [[1uxl\|1uxl]], [[1uxm\|1uxm]], [[2af2\|2af2]], [[2c9s\|2c9s]], [[2c9u\|2c9u]], [[2c9v\|2c9v]], [[2v0a\|2v0a]], [[2vr6\|2vr6]], [[2vr7\|2vr7]], [[2vr8\|2vr8]], [[2wko\|2wko]], [[2wyt\|2wyt]], [[2wyz\|2wyz]], [[2wz0\|2wz0]], [[2wz5\|2wz5]], [[2wz6\|2wz6]], [[2xjk\|2xjk]], [[2xjl\|2xjl]], [[4a7g\|4a7g]], [[4a7q\|4a7q]], [[4a7r\|4a7r]], [[4a7s\|4a7s]], [[4a7t\|4a7t]], [[4a7u\|4a7u]], [[4a7v\|4a7v]], [[4b3e\|4b3e]], [[4bcy\|4bcy]]</td></tr>
		+	<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Superoxide_dismutase Superoxide dismutase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.15.1.1 1.15.1.1] </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=4bcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bcz OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4bcz RCSB], [http://www.ebi.ac.uk/pdbsum/4bcz PDBsum]</span></td></tr>
		+	</table>
		+	== Disease ==
		+	[[http://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Defects in SOD1 are the cause of amyotrophic lateral sclerosis type 1 (ALS1) [MIM:[http://omim.org/entry/105400 105400]]. ALS1 is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of cases leading to familial forms.<ref>PMID:12963370</ref> <ref>PMID:19741096</ref> <ref>PMID:8528216</ref> <ref>PMID:8682505</ref> <ref>PMID:9541385</ref> <ref>PMID:12754496</ref> <ref>PMID:15056757</ref> <ref>PMID:18378676</ref> [:]<ref>PMID:8446170</ref> <ref>PMID:8351519</ref> <ref>PMID:8179602</ref> <ref>PMID:7980516</ref> <ref>PMID:8069312</ref> <ref>PMID:7951252</ref> <ref>PMID:7881433</ref> <ref>PMID:7836951</ref> <ref>PMID:7997024</ref> <ref>PMID:7870076</ref> <ref>PMID:7887412</ref> <ref>PMID:7795609</ref> <ref>PMID:7655468</ref> <ref>PMID:7655469</ref> <ref>PMID:7655471</ref> <ref>PMID:7700376</ref> <ref>PMID:7647793</ref> <ref>PMID:7501156</ref> <ref>PMID:7496169</ref> <ref>PMID:8938700</ref> <ref>PMID:8907321</ref> <ref>PMID:8990014</ref> <ref>PMID:9101297</ref> <ref>PMID:9455977</ref> <ref>PMID:10732812</ref> <ref>PMID:9131652</ref> <ref>PMID:10400992</ref> <ref>PMID:10430435</ref> <ref>PMID:11535232</ref> <ref>PMID:11369193</ref> <ref>PMID:12402272</ref> <ref>PMID:12145308</ref> <ref>PMID:14506936</ref> <ref>PMID:18552350</ref> <ref>PMID:18301754</ref> <ref>PMID:21247266</ref> <ref>PMID:21220647</ref>
		+	== Function ==
		+	[[http://www.uniprot.org/uniprot/SODC_HUMAN SODC_HUMAN]] Destroys radicals which are normally produced within the cells and which are toxic to biological systems.
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	The origin and biological role of dynamic motions of folded enzymes is not yet fully understood. In this study, we examine the molecular determinants for the dynamic motions within the beta-barrel of superoxide dismutase 1 (SOD1), which previously were implicated in allosteric regulation of protein maturation and also pathological misfolding in the neurodegenerative disease amyotrophic lateral sclerosis. Relaxation-dispersion NMR, hydrogen/deuterium exchange, and crystallographic data show that the dynamic motions are induced by the buried H43 side chain, which connects the backbones of the Cu ligand H120 and T39 by a hydrogen-bond linkage through the hydrophobic core. The functional role of this highly conserved H120-H43-T39 linkage is to strain H120 into the correct geometry for Cu binding. Upon elimination of the strain by mutation H43F, the apo protein relaxes through hydrogen-bond swapping into a more stable structure and the dynamic motions freeze out completely. At the same time, the holo protein becomes energetically penalized because the twisting back of H120 into Cu-bound geometry leads to burial of an unmatched backbone carbonyl group. The question then is whether this coupling between metal binding and global structural motions in the SOD1 molecule is an adverse side effect of evolving viable Cu coordination or plays a key role in allosteric regulation of biological function, or both?

-	~~{{STRUCTURE_4bcz\| PDB=4bcz \| SCENE= }}~~	+	Global structural motions from the strain of a single hydrogen bond.,Danielsson J, Awad W, Saraboji K, Kurnik M, Lang L, Leinartaite L, Marklund SL, Logan DT, Oliveberg M Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):3829-34. doi:, 10.1073/pnas.1217306110. Epub 2013 Feb 19. PMID:23431167<ref>PMID:23431167</ref>

-	~~===Monomeric Human Cu~~,~~Zn Superoxide dismutase, loops IV and VII deleted, apo form~~.~~===~~	+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>

-		+	==See Also==
-	==~~About this Structure~~==	+	*[[Superoxide Dismutase\|Superoxide Dismutase]]
-	[[~~4bcz~~]] ~~is a 2 chain structure with sequence from [http:~~//~~en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BCZ OCA].~~	+	== References ==
-	[[Category: ~~Homo sapiens~~]]	+	<references/>
		+	__TOC__
		+	</StructureSection>
		+	[[Category: Human]]
	[[Category: Superoxide dismutase]]		[[Category: Superoxide dismutase]]
-	[[Category: Awad, W.]]	+	[[Category: Awad, W]]
-	[[Category: Danielsson, J.]]	+	[[Category: Danielsson, J]]
-	[[Category: Kurnik, M.]]	+	[[Category: Kurnik, M]]
-	[[Category: Lang, L.]]	+	[[Category: Lang, L]]
-	[[Category: Logan, D T.]]	+	[[Category: Logan, D T]]
-	[[Category: Marklund, S L.]]	+	[[Category: Marklund, S L]]
-	[[Category: Oliveberg, M.]]	+	[[Category: Oliveberg, M]]
-	[[Category: Saraboji, K.]]	+	[[Category: Saraboji, K]]
	[[Category: Al]]		[[Category: Al]]
	[[Category: Cu/zn sod1]]		[[Category: Cu/zn sod1]]

OCA at 14:53, 27 February 2013

OCA — Wed, 27 Feb 2013 14:53:56 GMT

←Older revision		Revision as of 14:53, 27 February 2013
Line 1:		Line 1:
-	~~'''Unreleased structure'''~~	+	[[Image:4bcz.jpg\|left\|200px]]

-	~~The entry~~ 4bcz ~~is ON HOLD~~ ~~until Paper Publication~~	+	{{STRUCTURE_4bcz\| PDB=4bcz \| SCENE= }}

-	~~Authors: Saraboji~~, K., ~~Awad~~, ~~W., Danielsson, J., Lang, L., Kurnik, M., Marklund, S.L., Oliveberg, M., Logan, D.T~~.	+	===Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.===

-	~~Description~~: ~~Monomeric Human Cu,Zn~~ Superoxide dismutase, ~~loops IV and VII deleted~~, ~~apo form~~.	+
		+	==About this Structure==
		+	[[4bcz]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BCZ OCA].
		+	[[Category: Homo sapiens]]
		+	[[Category: Superoxide dismutase]]
		+	[[Category: Awad, W.]]
		+	[[Category: Danielsson, J.]]
		+	[[Category: Kurnik, M.]]
		+	[[Category: Lang, L.]]
		+	[[Category: Logan, D T.]]
		+	[[Category: Marklund, S L.]]
		+	[[Category: Oliveberg, M.]]
		+	[[Category: Saraboji, K.]]
		+	[[Category: Al]]
		+	[[Category: Cu/zn sod1]]
		+	[[Category: Disease mutation]]
		+	[[Category: Metal binding]]
		+	[[Category: Monomeric mutant]]
		+	[[Category: Neurodegeneration]]
		+	[[Category: Oxidoreductase]]

OCA at 10:51, 19 December 2012

OCA — Wed, 19 Dec 2012 10:51:43 GMT

←Older revision		Revision as of 10:51, 19 December 2012
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 4bcz is ON HOLD	+	The entry 4bcz is ON HOLD until Paper Publication

	Authors: Saraboji, K., Awad, W., Danielsson, J., Lang, L., Kurnik, M., Marklund, S.L., Oliveberg, M., Logan, D.T.		Authors: Saraboji, K., Awad, W., Danielsson, J., Lang, L., Kurnik, M., Marklund, S.L., Oliveberg, M., Logan, D.T.

	Description: Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.		Description: Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.

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

OCA — Wed, 10 Oct 2012 06:44:45 GMT

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

←Older revision

Revision as of 06:44, 10 October 2012

OCA: New page: '''Unreleased structure''' The entry 4bcz is ON HOLD Authors: Saraboji, K., Awad, W., Danielsson, J., Lang, L., Kurnik, M., Marklund, S.L., Oliveberg, M., Logan, D.T. Description: Mono...

OCA — Wed, 10 Oct 2012 06:44:44 GMT

New page: '''Unreleased structure''' The entry 4bcz is ON HOLD Authors: Saraboji, K., Awad, W., Danielsson, J., Lang, L., Kurnik, M., Marklund, S.L., Oliveberg, M., Logan, D.T. Description: Mono...

New page

'''Unreleased structure'''

The entry 4bcz is ON HOLD

Authors: Saraboji, K., Awad, W., Danielsson, J., Lang, L., Kurnik, M., Marklund, S.L., Oliveberg, M., Logan, D.T.

Description: Monomeric Human Cu,Zn Superoxide dismutase, loops IV and VII deleted, apo form.