4a04

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Current revision (11:17, 20 December 2023) (edit) (undo)
 
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<StructureSection load='4a04' size='340' side='right'caption='[[4a04]], [[Resolution|resolution]] 2.58&Aring;' scene=''>
<StructureSection load='4a04' size='340' side='right'caption='[[4a04]], [[Resolution|resolution]] 2.58&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<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>
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<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>
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</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>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.58&#8491;</td></tr>
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<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 ==
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[[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.
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[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 ==
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[[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).
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[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==
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Human]]
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[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Bhattacharya, S]]
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[[Category: Bhattacharya S]]
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[[Category: Ginn, H]]
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[[Category: De Mesmaeker J]]
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[[Category: Karia, D]]
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[[Category: El Omari K]]
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[[Category: Mancini, E J]]
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[[Category: Ginn H]]
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[[Category: Mesmaeker, J De]]
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[[Category: Karia D]]
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[[Category: Omari, K El]]
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[[Category: Mancini EJ]]
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[[Category: Protein-dna interaction]]
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[[Category: T-box protein]]
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[[Category: Transcription]]
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Current revision

Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome

PDB ID 4a04

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