1nfi: Difference between revisions
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1nfi]] is a 6 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=1NFI OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1NFI FirstGlance]. <br> | <table><tr><td colspan='2'>[[1nfi]] is a 6 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=1NFI OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1NFI FirstGlance]. <br> | ||
</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=1nfi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1nfi OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1nfi RCSB], [http://www.ebi.ac.uk/pdbsum/1nfi 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=1nfi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1nfi OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1nfi RCSB], [http://www.ebi.ac.uk/pdbsum/1nfi PDBsum]</span></td></tr> | ||
<table> | </table> | ||
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/IKBA_HUMAN IKBA_HUMAN]] Defects in NFKBIA are the cause of ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant (ADEDAID) [MIM:[http://omim.org/entry/612132 612132]]. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. ADEDAID is an ectodermal dysplasia associated with decreased production of pro-inflammatory cytokines and certain interferons, rendering patients susceptible to infection.<ref>PMID:14523047</ref> <ref>PMID:18412279</ref> | [[http://www.uniprot.org/uniprot/IKBA_HUMAN IKBA_HUMAN]] Defects in NFKBIA are the cause of ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant (ADEDAID) [MIM:[http://omim.org/entry/612132 612132]]. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. ADEDAID is an ectodermal dysplasia associated with decreased production of pro-inflammatory cytokines and certain interferons, rendering patients susceptible to infection.<ref>PMID:14523047</ref> <ref>PMID:18412279</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Harrison, S C | [[Category: Harrison, S C]] | ||
[[Category: Jacobs, M D | [[Category: Jacobs, M D]] | ||
[[Category: Ankyrin repeat]] | [[Category: Ankyrin repeat]] | ||
