OCA at 13:02, 1 November 2023

2023-11-01T13:02:32Z

←Older revision		Revision as of 13:02, 1 November 2023
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-	'''Unreleased structure'''

-	The entry ~~8bd0~~ is ~~ON HOLD~~ ~~until Paper Publication~~	+	==Human Gamma-D crystallin R36S mutant with DTT-Cystein Protein modification==
-		+	<StructureSection load='8bd0' size='340' side='right'caption='[[8bd0]], [[Resolution\|resolution]] 2.00Å' scene=''>
-	~~Authors~~:	+	== Structural highlights ==
-		+	<table><tr><td colspan='2'>[[8bd0]] 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=8BD0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8BD0 FirstGlance]. <br>
-	~~Description~~:	+	</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>
-	[[Category: ~~Unreleased~~ Structures]]	+	<tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CSO:S-HYDROXYCYSTEINE'>CSO</scene>, <scene name='pdbligand=DTT:2,3-DIHYDROXY-1,4-DITHIOBUTANE'>DTT</scene></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=8bd0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8bd0 OCA], [https://pdbe.org/8bd0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8bd0 RCSB], [https://www.ebi.ac.uk/pdbsum/8bd0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8bd0 ProSAT]</span></td></tr>
		+	</table>
		+	== Disease ==
		+	[https://www.uniprot.org/uniprot/CRGD_HUMAN CRGD_HUMAN] Defects in CRYGD are a cause of cataract autosomal dominant (ADC) [MIM:[https://omim.org/entry/604219 604219]. Cataract is an opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. Cataract is the most common treatable cause of visual disability in childhood.<ref>PMID:9927684</ref> <ref>PMID:10688888</ref> <ref>PMID:21031598</ref> Defects in CRYGD are the cause of cataract congenital non-nuclear polymorphic autosomal dominant (CCP) [MIM:[https://omim.org/entry/601286 601286]; also known as polymorphic congenital cataract. A congenital cataract characterized by a non-progressive phenotype and partial opacity that has a variable location between the fetal nucleus of the lens and the equator. The fetal nucleus is normal. The opacities are irregular and look similar to a bunch of grapes and may be present simultaneously in different lens layers.<ref>PMID:16943771</ref> <ref>PMID:17564961</ref> Defects in CRYGD are the cause of cataract congenital cerulean type 3 (CCA3) [MIM:[https://omim.org/entry/608983 608983]; also known as congenital cataract blue dot type 3. A cerulean form of autosomal dominant congenital cataract. Cerulean cataract is characterized by peripheral bluish and white opacifications organized in concentric layers with occasional central lesions arranged radially. The opacities are observed in the superficial layers of the fetal nucleus as well as the adult nucleus of the lens. Involvement is usually bilateral. Visual acuity is only mildly reduced in childhood. In adulthood, the opacifications may progress, making lens extraction necessary. Histologically the lesions are described as fusiform cavities between lens fibers which contain a deeply staining granular material. Although the lesions may take on various colors, a dull blue is the most common appearance and is responsible for the designation cerulean cataract. Defects in CRYGD are the cause of cataract crystalline aculeiform (CACA) [MIM:[https://omim.org/entry/115700 115700]. A congenital crystalline cataract characterized by fiberglass-like or needle-like crystals projecting in different directions, through or close to the axial region of the lens. The opacity causes a variable degree of vision loss.<ref>PMID:10521291</ref>
		+	== Function ==
		+	[https://www.uniprot.org/uniprot/CRGD_HUMAN CRGD_HUMAN] Crystallins are the dominant structural components of the vertebrate eye lens.
		+	== References ==
		+	<references/>
		+	__TOC__
		+	</StructureSection>
		+	[[Category: Homo sapiens]]
		+	[[Category: Large Structures]]
		+	[[Category: Hill JA]]
		+	[[Category: Yorke BA]]

OCA at 05:55, 21 December 2022

2022-12-21T05:55:06Z

←Older revision		Revision as of 05:55, 21 December 2022
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	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 8bd0 is ON HOLD	+	The entry 8bd0 is ON HOLD until Paper Publication

	Authors:		Authors:

OCA: Protected "8bd0" [edit=sysop:move=sysop]

2022-10-26T03:53:28Z

Protected "8bd0" [edit=sysop:move=sysop]

←Older revision

Revision as of 03:53, 26 October 2022

OCA: New page: '''Unreleased structure''' The entry 8bd0 is ON HOLD Authors: Description: Category: Unreleased Structures

2022-10-26T03:53:26Z

New page: '''Unreleased structure''' The entry 8bd0 is ON HOLD Authors: Description: Category: Unreleased Structures

New page

'''Unreleased structure'''

The entry 8bd0 is ON HOLD

Authors:

Description:
[[Category: Unreleased Structures]]

8bd0 - Revision history

OCA at 13:02, 1 November 2023

OCA at 05:55, 21 December 2022

OCA: Protected "8bd0" [edit=sysop:move=sysop]

OCA: New page: '''Unreleased structure''' The entry 8bd0 is ON HOLD Authors: Description: Category: Unreleased Structures