2gf1: Difference between revisions
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{{STRUCTURE_2gf1| PDB=2gf1 | SCENE= }} | {{STRUCTURE_2gf1| PDB=2gf1 | SCENE= }} | ||
===SOLUTION STRUCTURE OF HUMAN INSULIN-LIKE GROWTH FACTOR 1: A NUCLEAR MAGNETIC RESONANCE AND RESTRAINED MOLECULAR DYNAMICS STUDY=== | |||
{{ABSTRACT_PUBMED_2036417}} | |||
=== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/IGF1A_HUMAN IGF1A_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. | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/IGF1A_HUMAN IGF1A_HUMAN]] The insulin-like growth factors, isolated from plasma, are structurally and functionally related to insulin but have a much higher growth-promoting activity. May be a physiological regulator of [1-14C]-2-deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblasts. Stimulates glucose transport in rat bone-derived osteoblastic (PyMS) cells and is effective at much lower concentrations than insulin, not only regarding glycogen and DNA synthesis but also with regard to enhancing glucose uptake.<ref>PMID:21076856</ref> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:002036417</ref><references group="xtra"/> | <ref group="xtra">PMID:002036417</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Campbell, I D.]] | [[Category: Campbell, I D.]] | ||
