2wwu
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2wwu]] is a 1 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=2WWU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2WWU FirstGlance]. <br> | <table><tr><td colspan='2'>[[2wwu]] is a 1 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=2WWU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2WWU FirstGlance]. <br> | ||
- | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=BGC:BETA-D-GLUCOSE'>BGC</scene>, <scene name='pdbligand=NI:NICKEL+(II)+ION'>NI</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>< | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=BGC:BETA-D-GLUCOSE'>BGC</scene>, <scene name='pdbligand=NI:NICKEL+(II)+ION'>NI</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</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=2wwu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wwu OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2wwu RCSB], [http://www.ebi.ac.uk/pdbsum/2wwu 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=2wwu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2wwu OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2wwu RCSB], [http://www.ebi.ac.uk/pdbsum/2wwu PDBsum]</span></td></tr> |
- | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/PHF8_HUMAN PHF8_HUMAN]] Defects in PHF8 are the cause of mental retardation syndromic X-linked Siderius type (MRXSSD) [MIM:[http://omim.org/entry/300263 300263]]. A disorder characterized by mild to borderline mental retardation with or without cleft lip/cleft palate.<ref>PMID:20548336</ref> <ref>PMID:20346720</ref> <ref>PMID:20421419</ref> <ref>PMID:20208542</ref> <ref>PMID:20622853</ref> <ref>PMID:20622854</ref> <ref>PMID:20101266</ref> <ref>PMID:16199551</ref> <ref>PMID:17661819</ref> | [[http://www.uniprot.org/uniprot/PHF8_HUMAN PHF8_HUMAN]] Defects in PHF8 are the cause of mental retardation syndromic X-linked Siderius type (MRXSSD) [MIM:[http://omim.org/entry/300263 300263]]. A disorder characterized by mild to borderline mental retardation with or without cleft lip/cleft palate.<ref>PMID:20548336</ref> <ref>PMID:20346720</ref> <ref>PMID:20421419</ref> <ref>PMID:20208542</ref> <ref>PMID:20622853</ref> <ref>PMID:20622854</ref> <ref>PMID:20101266</ref> <ref>PMID:16199551</ref> <ref>PMID:17661819</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Allerston, C | + | [[Category: Allerston, C]] |
- | [[Category: Arrowsmith, C | + | [[Category: Arrowsmith, C]] |
- | [[Category: Bountra, C | + | [[Category: Bountra, C]] |
- | [[Category: Cooper, C | + | [[Category: Cooper, C]] |
- | [[Category: Delft, F Von | + | [[Category: Delft, F Von]] |
- | [[Category: Edwards, A | + | [[Category: Edwards, A]] |
- | [[Category: Hozjan, V | + | [[Category: Hozjan, V]] |
- | [[Category: Kavanagh, K L | + | [[Category: Kavanagh, K L]] |
- | [[Category: Krojer, T | + | [[Category: Krojer, T]] |
- | [[Category: Mcdonough, M A | + | [[Category: Mcdonough, M A]] |
- | [[Category: Muniz, J | + | [[Category: Muniz, J]] |
- | [[Category: Oppermann, U | + | [[Category: Oppermann, U]] |
- | [[Category: Salah, E | + | [[Category: Salah, E]] |
- | [[Category: Schofield, C J | + | [[Category: Schofield, C J]] |
- | [[Category: Tumber, A | + | [[Category: Tumber, A]] |
- | [[Category: Weigelt, J | + | [[Category: Weigelt, J]] |
- | [[Category: Yue, W W | + | [[Category: Yue, W W]] |
[[Category: Epigenetic]] | [[Category: Epigenetic]] | ||
[[Category: Histone demethylase]] | [[Category: Histone demethylase]] | ||
[[Category: Jmjc domain]] | [[Category: Jmjc domain]] | ||
[[Category: Metal-binding protein]] | [[Category: Metal-binding protein]] |
Revision as of 07:57, 20 January 2015
Crystal structure of the catalytic domain of PHD finger protein 8
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Categories: Homo sapiens | Allerston, C | Arrowsmith, C | Bountra, C | Cooper, C | Delft, F Von | Edwards, A | Hozjan, V | Kavanagh, K L | Krojer, T | Mcdonough, M A | Muniz, J | Oppermann, U | Salah, E | Schofield, C J | Tumber, A | Weigelt, J | Yue, W W | Epigenetic | Histone demethylase | Jmjc domain | Metal-binding protein