1wqj
From Proteopedia
(Difference between revisions)
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<StructureSection load='1wqj' size='340' side='right'caption='[[1wqj]], [[Resolution|resolution]] 1.60Å' scene=''> | <StructureSection load='1wqj' size='340' side='right'caption='[[1wqj]], [[Resolution|resolution]] 1.60Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[1wqj]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[1wqj]] is a 2 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=1WQJ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1WQJ FirstGlance]. <br> |
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.6Å</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=1wqj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wqj OCA], [https://pdbe.org/1wqj PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1wqj RCSB], [https://www.ebi.ac.uk/pdbsum/1wqj PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1wqj ProSAT]</span></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=1wqj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wqj OCA], [https://pdbe.org/1wqj PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1wqj RCSB], [https://www.ebi.ac.uk/pdbsum/1wqj PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1wqj ProSAT]</span></td></tr> | ||
</table> | </table> | ||
- | == Disease == | ||
- | [[https://www.uniprot.org/uniprot/IGF1_HUMAN IGF1_HUMAN]] Defects in IGF1 are the cause of insulin-like growth factor I deficiency (IGF1 deficiency) [MIM:[https://omim.org/entry/608747 608747]]. IGF1 deficiency is an autosomal recessive disorder characterized by growth retardation, sensorineural deafness and mental retardation. | ||
== Function == | == Function == | ||
- | + | [https://www.uniprot.org/uniprot/IBP4_HUMAN IBP4_HUMAN] IGF-binding proteins prolong the half-life of the IGFs and have been shown to either inhibit or stimulate the growth promoting effects of the IGFs on cell culture. They alter the interaction of IGFs with their cell surface receptors. | |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Engh | + | [[Category: Engh RA]] |
- | [[Category: Holak | + | [[Category: Holak TA]] |
- | [[Category: Huber | + | [[Category: Huber R]] |
- | [[Category: Kuenkele | + | [[Category: Kuenkele KP]] |
- | [[Category: Lang | + | [[Category: Lang K]] |
- | [[Category: Popowicz | + | [[Category: Popowicz GM]] |
- | [[Category: Siwanowicz | + | [[Category: Siwanowicz I]] |
- | [[Category: Wisniewska | + | [[Category: Wisniewska M]] |
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Revision as of 07:58, 25 October 2023
Structural Basis for the Regulation of Insulin-Like Growth Factors (IGFs) by IGF Binding Proteins (IGFBPs)
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Categories: Homo sapiens | Large Structures | Engh RA | Holak TA | Huber R | Kuenkele KP | Lang K | Popowicz GM | Siwanowicz I | Wisniewska M