2l29: Difference between revisions

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~~[[Image:2l29.png|left|200px]]~~

===Complex structure of E4 mutant human IGF2R domain 11 bound to IGF-II===

===~~Complex structure~~ of ~~E4 mutant human IGF2R domain 11 bound to IGF~~-~~II===~~

==Disease==

[[http://www.uniprot.org/uniprot/IGF2_HUMAN IGF2_HUMAN]] Epigenetic changes of DNA hypomethylation in IGF2 are a cause of Silver-Russell syndrome (SRS) [MIM:[http://omim.org/entry/180860 180860]]. A clinically heterogeneous condition characterized by severe intrauterine growth retardation, poor postnatal growth, craniofacial features such as a triangular shaped face and a broad forehead, body asymmetry, and a variety of minor malformations. The phenotypic expression changes during childhood and adolescence, with the facial features and asymmetry usually becoming more subtle with age.<ref>PMID:19066168</ref>

~~{{ABSTRACT_PUBMED_23197533}}~~

==Function==

[[http://www.uniprot.org/uniprot/IGF2_HUMAN IGF2_HUMAN]] The insulin-like growth factors possess growth-promoting activity. In vitro, they are potent mitogens for cultured cells. IGF-II is influenced by placental lactogen and may play a role in fetal development.<ref>PMID:16912056</ref> Preptin undergoes glucose-mediated co-secretion with insulin, and acts as physiological amplifier of glucose-mediated insulin secretion. Exhibits osteogenic properties by increasing osteoblast mitogenic activity through phosphoactivation of MAPK1 and MAPK3.<ref>PMID:16912056</ref>

==About this Structure==

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==See Also==

*[[Insulin-like growth factor receptor|Insulin-like growth factor receptor]]

==Reference==

[[Category: Homo sapiens]]

[[Category: Crump, M P.]]

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@@ Line 1: / Line 1: @@
-[[Image:2l29.png|left|200px]]
 {{STRUCTURE_2l29|  PDB=2l29  |  SCENE=  }}
+===Complex structure of E4 mutant human IGF2R domain 11 bound to IGF-II===
+{{ABSTRACT_PUBMED_23197533}}
-===Complex structure of E4 mutant human IGF2R domain 11 bound to IGF-II===
+==Disease==
+[[http://www.uniprot.org/uniprot/IGF2_HUMAN IGF2_HUMAN]] Epigenetic changes of DNA hypomethylation in IGF2 are a cause of Silver-Russell syndrome (SRS) [MIM:[http://omim.org/entry/180860 180860]]. A clinically heterogeneous condition characterized by severe intrauterine growth retardation, poor postnatal growth, craniofacial features such as a triangular shaped face and a broad forehead, body asymmetry, and a variety of minor malformations. The phenotypic expression changes during childhood and adolescence, with the facial features and asymmetry usually becoming more subtle with age.<ref>PMID:19066168</ref>
-{{ABSTRACT_PUBMED_23197533}}
+==Function==
+[[http://www.uniprot.org/uniprot/IGF2_HUMAN IGF2_HUMAN]] The insulin-like growth factors possess growth-promoting activity. In vitro, they are potent mitogens for cultured cells. IGF-II is influenced by placental lactogen and may play a role in fetal development.<ref>PMID:16912056</ref>  Preptin undergoes glucose-mediated co-secretion with insulin, and acts as physiological amplifier of glucose-mediated insulin secretion. Exhibits osteogenic properties by increasing osteoblast mitogenic activity through phosphoactivation of MAPK1 and MAPK3.<ref>PMID:16912056</ref>
 ==About this Structure==
@@ Line 12: / Line 14: @@
 ==See Also==
 *[[Insulin-like growth factor receptor|Insulin-like growth factor receptor]]
+==Reference==
+<references group="xtra"/><references/>
 [[Category: Homo sapiens]]
 [[Category: Crump, M P.]]