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1f62
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1f62]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1F62 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1F62 FirstGlance]. <br> | <table><tr><td colspan='2'>[[1f62]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1F62 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1F62 FirstGlance]. <br> | ||
| - | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>< | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> |
| - | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1f62 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1f62 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1f62 RCSB], [http://www.ebi.ac.uk/pdbsum/1f62 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=1f62 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1f62 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1f62 RCSB], [http://www.ebi.ac.uk/pdbsum/1f62 PDBsum]</span></td></tr> |
| - | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/BAZ1B_HUMAN BAZ1B_HUMAN]] Note=BAZ1B is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of BAZ1B may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease.<ref>PMID:9828126</ref> | [[http://www.uniprot.org/uniprot/BAZ1B_HUMAN BAZ1B_HUMAN]] Note=BAZ1B is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of BAZ1B may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease.<ref>PMID:9828126</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Dyson, H J | + | [[Category: Dyson, H J]] |
| - | [[Category: Martinez-Yamout, M | + | [[Category: Martinez-Yamout, M]] |
| - | [[Category: Pascual, J | + | [[Category: Pascual, J]] |
| - | [[Category: Wright, P E | + | [[Category: Wright, P E]] |
[[Category: Transcription]] | [[Category: Transcription]] | ||
[[Category: Zn-finger]] | [[Category: Zn-finger]] | ||
Revision as of 19:37, 22 December 2014
WSTF-PHD
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