2wr6
From Proteopedia
(Difference between revisions)
m (Protected "2wr6" [edit=sysop:move=sysop]) |
|||
Line 1: | Line 1: | ||
- | [[Image:2wr6.png|left|200px]] | ||
- | |||
{{STRUCTURE_2wr6| PDB=2wr6 | SCENE= }} | {{STRUCTURE_2wr6| PDB=2wr6 | SCENE= }} | ||
+ | ===STRUCTURE OF THE COMPLEX OF RBP4 WITH LINOLEIC ACID=== | ||
- | === | + | ==Disease== |
+ | [[http://www.uniprot.org/uniprot/RET4_HUMAN RET4_HUMAN]] Defects in RBP4 are a cause of retinol-binding protein deficiency (RBP deficiency) [MIM:[http://omim.org/entry/180250 180250]]. This condition causes night vision problems. It produces a typical 'fundus xerophthalmicus', featuring a progressed atrophy of the retinal pigment epithelium. | ||
+ | ==Function== | ||
+ | [[http://www.uniprot.org/uniprot/RET4_HUMAN RET4_HUMAN]] Delivers retinol from the liver stores to the peripheral tissues. In plasma, the RBP-retinol complex interacts with transthyretin, this prevents its loss by filtration through the kidney glomeruli. | ||
==About this Structure== | ==About this Structure== |
Revision as of 06:03, 25 March 2013
Contents |
STRUCTURE OF THE COMPLEX OF RBP4 WITH LINOLEIC ACID
Disease
[RET4_HUMAN] Defects in RBP4 are a cause of retinol-binding protein deficiency (RBP deficiency) [MIM:180250]. This condition causes night vision problems. It produces a typical 'fundus xerophthalmicus', featuring a progressed atrophy of the retinal pigment epithelium.
Function
[RET4_HUMAN] Delivers retinol from the liver stores to the peripheral tissues. In plasma, the RBP-retinol complex interacts with transthyretin, this prevents its loss by filtration through the kidney glomeruli.
About this Structure
2wr6 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.