This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


5l3m

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
m (Protected "5l3m" [edit=sysop:move=sysop])
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 5l3m is ON HOLD
+
==D11 bound [S39_PQ]-IGF-II==
-
 
+
<StructureSection load='5l3m' size='340' side='right' caption='[[5l3m]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
-
Authors: Hexnerova, R.
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[5l3m]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5L3M OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5L3M FirstGlance]. <br>
-
Description: D11 bound [S39_PQ]-IGF-II
+
</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=5l3m FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5l3m OCA], [http://pdbe.org/5l3m PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5l3m RCSB], [http://www.ebi.ac.uk/pdbsum/5l3m PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5l3m ProSAT]</span></td></tr>
-
[[Category: Unreleased Structures]]
+
</table>
 +
== 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>
 +
== 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>
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
[[Category: Hexnerova, R]]
[[Category: Hexnerova, R]]
 +
[[Category: Cell cycle]]
 +
[[Category: Igf-ii]]

Revision as of 16:31, 10 August 2016

D11 bound [S39_PQ]-IGF-II

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools