1wqj
From Proteopedia
(Difference between revisions)
Line 3: | Line 3: | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1wqj]] is a 2 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=1WQJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1WQJ FirstGlance]. <br> | <table><tr><td colspan='2'>[[1wqj]] is a 2 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=1WQJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1WQJ FirstGlance]. <br> | ||
- | </td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1h59|1h59]]</td></tr> | + | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1h59|1h59]]</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=1wqj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wqj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1wqj RCSB], [http://www.ebi.ac.uk/pdbsum/1wqj 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=1wqj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wqj OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1wqj RCSB], [http://www.ebi.ac.uk/pdbsum/1wqj PDBsum]</span></td></tr> |
- | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/IGF1B_HUMAN IGF1B_HUMAN]] Defects in IGF1 are the cause of insulin-like growth factor I deficiency (IGF1 deficiency) [MIM:[http://omim.org/entry/608747 608747]]. IGF1 deficiency is an autosomal recessive disorder characterized by growth retardation, sensorineural deafness and mental retardation. | [[http://www.uniprot.org/uniprot/IGF1B_HUMAN IGF1B_HUMAN]] Defects in IGF1 are the cause of insulin-like growth factor I deficiency (IGF1 deficiency) [MIM:[http://omim.org/entry/608747 608747]]. IGF1 deficiency is an autosomal recessive disorder characterized by growth retardation, sensorineural deafness and mental retardation. | ||
Line 36: | Line 36: | ||
</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Engh, R A | + | [[Category: Engh, R A]] |
- | [[Category: Holak, T A | + | [[Category: Holak, T A]] |
- | [[Category: Huber, R | + | [[Category: Huber, R]] |
- | [[Category: Kuenkele, K P | + | [[Category: Kuenkele, K P]] |
- | [[Category: Lang, K | + | [[Category: Lang, K]] |
- | [[Category: Popowicz, G M | + | [[Category: Popowicz, G M]] |
- | [[Category: Siwanowicz, I | + | [[Category: Siwanowicz, I]] |
- | [[Category: Wisniewska, M | + | [[Category: Wisniewska, M]] |
[[Category: Disulfide bond ladder]] | [[Category: Disulfide bond ladder]] | ||
[[Category: Disulfide rich]] | [[Category: Disulfide rich]] | ||
[[Category: Protein binding-hormone-growth factor complex]] | [[Category: Protein binding-hormone-growth factor complex]] | ||
[[Category: Protein-protein complex]] | [[Category: Protein-protein complex]] |
Revision as of 13:32, 6 January 2015
Structural Basis for the Regulation of Insulin-Like Growth Factors (IGFs) by IGF Binding Proteins (IGFBPs)
|