2h8b
From Proteopedia
(Difference between revisions)
m (Protected "2h8b" [edit=sysop:move=sysop]) |
|||
Line 1: | Line 1: | ||
- | [[Image:2h8b.png|left|200px]] | ||
- | |||
{{STRUCTURE_2h8b| PDB=2h8b | SCENE= }} | {{STRUCTURE_2h8b| PDB=2h8b | SCENE= }} | ||
- | |||
===Solution structure of INSL3=== | ===Solution structure of INSL3=== | ||
+ | {{ABSTRACT_PUBMED_16867980}} | ||
- | + | ==Disease== | |
+ | [[http://www.uniprot.org/uniprot/INSL3_HUMAN INSL3_HUMAN]] Defects in INSL3 seems to be a cause of cryptorchidism (CRYPTO) [MIM:[http://omim.org/entry/219050 219050]]; also known as impaired testicular descent. It is one of the most frequent congenital abnormalities in humans, involving 2-5% of male births. Cryptorchidism is associated with increased risk of infertility and testicular cancer. The frequency of INSL3 gene mutations as a cause of cryptorchidism is low.<ref>PMID:11095425</ref><ref>PMID:11746019</ref><ref>PMID:12601553</ref> | ||
+ | |||
+ | ==Function== | ||
+ | [[http://www.uniprot.org/uniprot/INSL3_HUMAN INSL3_HUMAN]] Seems to play a role in testicular function. May be a trophic hormone with a role in testicular descent in fetal life. Is a ligand for LGR8 receptor. | ||
==About this Structure== | ==About this Structure== | ||
Line 11: | Line 13: | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID:016867980</ref><references group="xtra"/> | + | <ref group="xtra">PMID:016867980</ref><references group="xtra"/><references/> |
[[Category: Craik, D J.]] | [[Category: Craik, D J.]] | ||
[[Category: Daly, N L.]] | [[Category: Daly, N L.]] |
Revision as of 11:49, 24 March 2013
Contents |
Solution structure of INSL3
Template:ABSTRACT PUBMED 16867980
Disease
[INSL3_HUMAN] Defects in INSL3 seems to be a cause of cryptorchidism (CRYPTO) [MIM:219050]; also known as impaired testicular descent. It is one of the most frequent congenital abnormalities in humans, involving 2-5% of male births. Cryptorchidism is associated with increased risk of infertility and testicular cancer. The frequency of INSL3 gene mutations as a cause of cryptorchidism is low.[1][2][3]
Function
[INSL3_HUMAN] Seems to play a role in testicular function. May be a trophic hormone with a role in testicular descent in fetal life. Is a ligand for LGR8 receptor.
About this Structure
2h8b is a 2 chain structure. Full experimental information is available from OCA.
Reference
- Rosengren KJ, Zhang S, Lin F, Daly NL, Scott DJ, Hughes RA, Bathgate RA, Craik DJ, Wade JD. Solution structure and characterization of the LGR8 receptor binding surface of insulin-like peptide 3. J Biol Chem. 2006 Sep 22;281(38):28287-95. Epub 2006 Jul 25. PMID:16867980 doi:10.1074/jbc.M603829200
- ↑ Tomboc M, Lee PA, Mitwally MF, Schneck FX, Bellinger M, Witchel SF. Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism. J Clin Endocrinol Metab. 2000 Nov;85(11):4013-8. PMID:11095425
- ↑ Marin P, Ferlin A, Moro E, Rossi A, Bartoloni L, Rossato M, Foresta C. Novel insulin-like 3 (INSL3) gene mutation associated with human cryptorchidism. Am J Med Genet. 2001 Nov 1;103(4):348-9. PMID:11746019
- ↑ Canto P, Escudero I, Soderlund D, Nishimura E, Carranza-Lira S, Gutierrez J, Nava A, Mendez JP. A novel mutation of the insulin-like 3 gene in patients with cryptorchidism. J Hum Genet. 2003;48(2):86-90. PMID:12601553 doi:10.1007/s100380300012