4a04 - Revision history

OCA at 11:17, 20 December 2023

2023-12-20T11:17:11Z

←Older revision		Revision as of 11:17, 20 December 2023
Line 3:		Line 3:
	<StructureSection load='4a04' size='340' side='right'caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>		<StructureSection load='4a04' size='340' side='right'caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[4a04]] is a 4 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=4A04 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4A04 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[4a04]] is a 4 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=4A04 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4A04 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=4a04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a04 OCA], [https://pdbe.org/4a04 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4a04 RCSB], [https://www.ebi.ac.uk/pdbsum/4a04 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4a04 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]] 2.58Å</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=4a04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a04 OCA], [https://pdbe.org/4a04 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4a04 RCSB], [https://www.ebi.ac.uk/pdbsum/4a04 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4a04 ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
-	[[https://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] 22q11.2 microduplication syndrome;22q11.2 deletion syndrome. Haploinsufficiency of the TBX1 gene is responsible for most of the physical malformations present in DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). DGS is characterized by the association of several malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal cardiopathy, and a subtle but characteristic facial dysmorphology. VCFS is marked by the association of congenital conotruncal heart defects, cleft palate or velar insufficiency, facial dysmorpholgy and learning difficulties. It is now accepted that these two syndromes represent two forms of clinical expression of the same entity manifesting at different stages of life. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.	+	[https://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN] 22q11.2 microduplication syndrome;22q11.2 deletion syndrome. Haploinsufficiency of the TBX1 gene is responsible for most of the physical malformations present in DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). DGS is characterized by the association of several malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal cardiopathy, and a subtle but characteristic facial dysmorphology. VCFS is marked by the association of congenital conotruncal heart defects, cleft palate or velar insufficiency, facial dysmorpholgy and learning difficulties. It is now accepted that these two syndromes represent two forms of clinical expression of the same entity manifesting at different stages of life. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
	== Function ==		== Function ==
-	[[https://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] Probable transcriptional regulator involved in developmental processes. Is required for normal development of the pharyngeal arch arteries (By similarity).	+	[https://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN] Probable transcriptional regulator involved in developmental processes. Is required for normal development of the pharyngeal arch arteries (By similarity).

	==See Also==		==See Also==
Line 15:		Line 16:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: Bhattacharya, S]]	+	[[Category: Bhattacharya S]]
-	[[Category: ~~Ginn, H]]~~	+	[[Category: De Mesmaeker J]]
-	~~[[Category: Karia, D]]~~	+	[[Category: El Omari K]]
-	~~[[Category: Mancini, E J]]~~	+	[[Category: Ginn H]]
-	~~[[Category:~~ Mesmaeker, J De]]	+	[[Category: Karia D]]
-	[[Category: Omari, K El]]	+	[[Category: Mancini EJ]]
-	[[Category: ~~Protein-dna interaction~~]]	+
-	[[Category: ~~T-box protein~~]]	+
-	[[Category: ~~Transcription~~]]	+

OCA at 07:36, 18 August 2022

2022-08-18T07:36:07Z

←Older revision		Revision as of 07:36, 18 August 2022
Line 1:		Line 1:

	==Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome==		==Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome==
-	<StructureSection load='4a04' size='340' side='right' caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>	+	<StructureSection load='4a04' size='340' side='right'caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[4a04]] is a 4 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=4A04 OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=4A04 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[4a04]] is a 4 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=4A04 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4A04 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=4a04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a04 OCA], [~~http~~://pdbe.org/4a04 PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=4a04 RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/4a04 PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=4a04 ProSAT]</span></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=4a04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a04 OCA], [https://pdbe.org/4a04 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4a04 RCSB], [https://www.ebi.ac.uk/pdbsum/4a04 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4a04 ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
-	[[~~http~~://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] 22q11.2 microduplication syndrome;22q11.2 deletion syndrome. Haploinsufficiency of the TBX1 gene is responsible for most of the physical malformations present in DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). DGS is characterized by the association of several malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal cardiopathy, and a subtle but characteristic facial dysmorphology. VCFS is marked by the association of congenital conotruncal heart defects, cleft palate or velar insufficiency, facial dysmorpholgy and learning difficulties. It is now accepted that these two syndromes represent two forms of clinical expression of the same entity manifesting at different stages of life. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.	+	[[https://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] 22q11.2 microduplication syndrome;22q11.2 deletion syndrome. Haploinsufficiency of the TBX1 gene is responsible for most of the physical malformations present in DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). DGS is characterized by the association of several malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal cardiopathy, and a subtle but characteristic facial dysmorphology. VCFS is marked by the association of congenital conotruncal heart defects, cleft palate or velar insufficiency, facial dysmorpholgy and learning difficulties. It is now accepted that these two syndromes represent two forms of clinical expression of the same entity manifesting at different stages of life. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
	== Function ==		== Function ==
-	[[~~http~~://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] Probable transcriptional regulator involved in developmental processes. Is required for normal development of the pharyngeal arch arteries (By similarity).	+	[[https://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] Probable transcriptional regulator involved in developmental processes. Is required for normal development of the pharyngeal arch arteries (By similarity).

	==See Also==		==See Also==
Line 16:		Line 16:
	</StructureSection>		</StructureSection>
	[[Category: Human]]		[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Bhattacharya, S]]		[[Category: Bhattacharya, S]]
	[[Category: Ginn, H]]		[[Category: Ginn, H]]

OCA at 17:10, 27 February 2019

2019-02-27T17:10:41Z

←Older revision		Revision as of 17:10, 27 February 2019
Line 1:		Line 1:

-	==Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.==	+	==Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome==
	<StructureSection load='4a04' size='340' side='right' caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>		<StructureSection load='4a04' size='340' side='right' caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>
	== Structural highlights ==		== Structural highlights ==

OCA at 03:48, 5 August 2016

2016-08-05T03:48:39Z

←Older revision		Revision as of 03:48, 5 August 2016
Line 1:		Line 1:
		+
	==Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.==		==Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.==
	<StructureSection load='4a04' size='340' side='right' caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>		<StructureSection load='4a04' size='340' side='right' caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[4a04]] is a 4 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=4A04 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4A04 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[4a04]] is a 4 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=4A04 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4A04 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=4a04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a04 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4a04 RCSB], [http://www.ebi.ac.uk/pdbsum/4a04 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=4a04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a04 OCA], [http://pdbe.org/4a04 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4a04 RCSB], [http://www.ebi.ac.uk/pdbsum/4a04 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4a04 ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
Line 14:		Line 15:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Homo sapiens~~]]	+	[[Category: Human]]
	[[Category: Bhattacharya, S]]		[[Category: Bhattacharya, S]]
	[[Category: Ginn, H]]		[[Category: Ginn, H]]

OCA at 08:46, 18 December 2014

2014-12-18T08:46:16Z

←Older revision		Revision as of 08:46, 18 December 2014
Line 1:		Line 1:
-	~~{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}~~	+	==Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.==
-	===Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.===	+	<StructureSection load='4a04' size='340' side='right' caption='[[4a04]], [[Resolution\|resolution]] 2.58Å' scene=''>
-		+	== Structural highlights ==
-	==~~About this Structure~~==	+	<table><tr><td colspan='2'>[[4a04]] is a 4 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=4A04 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4A04 FirstGlance]. <br>
-	[[4a04]] is a 4 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=4A04 OCA].	+	</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=4a04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a04 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4a04 RCSB], [http://www.ebi.ac.uk/pdbsum/4a04 PDBsum]</span></td></tr>
		+	</table>
		+	== Disease ==
		+	[[http://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] 22q11.2 microduplication syndrome;22q11.2 deletion syndrome. Haploinsufficiency of the TBX1 gene is responsible for most of the physical malformations present in DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). DGS is characterized by the association of several malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal cardiopathy, and a subtle but characteristic facial dysmorphology. VCFS is marked by the association of congenital conotruncal heart defects, cleft palate or velar insufficiency, facial dysmorpholgy and learning difficulties. It is now accepted that these two syndromes represent two forms of clinical expression of the same entity manifesting at different stages of life. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
		+	== Function ==
		+	[[http://www.uniprot.org/uniprot/TBX1_HUMAN TBX1_HUMAN]] Probable transcriptional regulator involved in developmental processes. Is required for normal development of the pharyngeal arch arteries (By similarity).

	==See Also==		==See Also==
	*[[T-box proteins\|T-box proteins]]		*[[T-box proteins\|T-box proteins]]
-		+	__TOC__
-	~~==Reference==~~	+	</StructureSection>
-	~~<ref group="xtra">PMID:022095455</ref>~~<~~references group="xtra"~~/>	+
	[[Category: Homo sapiens]]		[[Category: Homo sapiens]]
-	[[Category: Bhattacharya, S.]]	+	[[Category: Bhattacharya, S]]
-	[[Category: Ginn, H.]]	+	[[Category: Ginn, H]]
-	[[Category: Karia, D.]]	+	[[Category: Karia, D]]
-	[[Category: Mancini, E J.]]	+	[[Category: Mancini, E J]]
-	[[Category: Mesmaeker, J De.]]	+	[[Category: Mesmaeker, J De]]
-	[[Category: Omari, K El.]]	+	[[Category: Omari, K El]]
	[[Category: Protein-dna interaction]]		[[Category: Protein-dna interaction]]
	[[Category: T-box protein]]		[[Category: T-box protein]]
	[[Category: Transcription]]		[[Category: Transcription]]

OCA at 09:37, 11 March 2013

2013-03-11T09:37:40Z

←Older revision		Revision as of 09:37, 11 March 2013
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-	[[Image:4a04.png\|left\|200px]]
-
	{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}		{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}
-
	===Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.===		===Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.===
-

	==About this Structure==		==About this Structure==

OCA at 05:26, 12 September 2012

2012-09-12T05:26:58Z

←Older revision		Revision as of 05:26, 12 September 2012
Line 1:		Line 1:
	[[Image:4a04.png\|left\|200px]]		[[Image:4a04.png\|left\|200px]]

-	<!--
-	The line below this paragraph, containing "STRUCTURE_4a04", creates the "Structure Box" on the page.
-	You may change the PDB parameter (which sets the PDB file loaded into the applet)
-	or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-	or leave the SCENE parameter empty for the default display.
-	-->
	{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}		{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}

-	===~~TBC~~===	+	===Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome.===

OCA at 07:09, 18 April 2012

2012-04-18T07:09:12Z

←Older revision		Revision as of 07:09, 18 April 2012
Line 9:		Line 9:
	{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}		{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}

-	===~~STRUCTURE OF THE DNA-BOUND T-BOX DOMAIN OF HUMAN TBX1, A TRANSCRIPTION FACTOR ASSOCIATED WITH THE DIGEORGE SYNDROME~~===	+	===TBC===


	==About this Structure==		==About this Structure==
	[[4a04]] is a 4 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=4A04 OCA].		[[4a04]] is a 4 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=4A04 OCA].
		+
		+	==See Also==
		+	*[[T-box proteins\|T-box proteins]]

	==Reference==		==Reference==

OCA at 05:38, 30 November 2011

2011-11-30T05:38:12Z

←Older revision		Revision as of 05:38, 30 November 2011
Line 14:		Line 14:
	==About this Structure==		==About this Structure==
	[[4a04]] is a 4 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=4A04 OCA].		[[4a04]] is a 4 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=4A04 OCA].
		+
		+	==Reference==
		+	<ref group="xtra">PMID:022095455</ref><references group="xtra"/>
	[[Category: Homo sapiens]]		[[Category: Homo sapiens]]
	[[Category: Bhattacharya, S.]]		[[Category: Bhattacharya, S.]]

OCA at 08:21, 30 October 2011

2011-10-30T08:21:32Z

←Older revision		Revision as of 08:21, 30 October 2011
Line 1:		Line 1:
-	~~'''Unreleased structure'''~~	+	[[Image:4a04.png\|left\|200px]]

-	The ~~entry 4a04~~ is ~~ON HOLD~~ ~~until Paper Publication~~	+	<!--
		+	The line below this paragraph, containing "STRUCTURE_4a04", creates the "Structure Box" on the page.
		+	You may change the PDB parameter (which sets the PDB file loaded into the applet)
		+	or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
		+	or leave the SCENE parameter empty for the default display.
		+	-->
		+	{{STRUCTURE_4a04\| PDB=4a04 \| SCENE= }}

-	~~Authors: El Omari~~, ~~K., De Mesmaeker, J., Karia, D., Ginn, H., Bhattacharya, S., Mancini, E.J.~~	+	===STRUCTURE OF THE DNA-BOUND T-BOX DOMAIN OF HUMAN TBX1, A TRANSCRIPTION FACTOR ASSOCIATED WITH THE DIGEORGE SYNDROME===

-	~~Description~~:	+
		+	==About this Structure==
		+	[[4a04]] is a 4 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=4A04 OCA].
		+	[[Category: Homo sapiens]]
		+	[[Category: Bhattacharya, S.]]
		+	[[Category: Ginn, H.]]
		+	[[Category: Karia, D.]]
		+	[[Category: Mancini, E J.]]
		+	[[Category: Mesmaeker, J De.]]
		+	[[Category: Omari, K El.]]
		+	[[Category: Protein-dna interaction]]
		+	[[Category: T-box protein]]
		+	[[Category: Transcription]]