4iy3: Difference between revisions

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'''Unreleased structure'''
==Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4==
 
<StructureSection load='4iy3' size='340' side='right' caption='[[4iy3]], [[Resolution|resolution]] 3.60&Aring;' scene=''>
The entry 4iy3 is ON HOLD  until Paper Publication
== Structural highlights ==
 
<table><tr><td colspan='2'>[[4iy3]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4IY3 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4IY3 FirstGlance]. <br>
Authors: Corral-Rodriguez, M.A., Stuiver, M., Encinar, J.A., Spiwok, V., Gomez-Garcia, I., Oyenarte, I., Ereno-Orbea, J., Terashima, H., Accardi, A., Diercks, T., Muller, D., Martinez-Cruz, L.A.
</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4iy0|4iy0]], [[4iy2|4iy2]], [[4iy4|4iy4]]</td></tr>
 
<tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CNNM4 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
Description: Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4
<tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4iy3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4iy3 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4iy3 RCSB], [http://www.ebi.ac.uk/pdbsum/4iy3 PDBsum]</span></td></tr>
<table>
== Disease ==
[[http://www.uniprot.org/uniprot/CNNM4_HUMAN CNNM4_HUMAN]] Jalili syndrome. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[[http://www.uniprot.org/uniprot/CNNM4_HUMAN CNNM4_HUMAN]] Probable metal transporter. The interaction with the metal ion chaperone COX11 suggests that it may play a role in sensory neuron functions (By similarity). May play a role in biomineralization and retinal function.<ref>PMID:19200527</ref> <ref>PMID:19200525</ref> 
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Human]]
[[Category: Accardi, A.]]
[[Category: Corral-Rodriguez, M A.]]
[[Category: Diercks, T.]]
[[Category: Encinar, J A.]]
[[Category: Ereno-Orbea, J.]]
[[Category: Gomez-Garcia, I.]]
[[Category: Martinez-Cruz, L A.]]
[[Category: Muller, D.]]
[[Category: Oyenarte, I.]]
[[Category: Spiwok, V.]]
[[Category: Stuiver, M.]]
[[Category: Terashima, H.]]
[[Category: Cbs domain]]
[[Category: Cytosol]]
[[Category: Magnesium transport]]
[[Category: Metal transport]]

Revision as of 15:05, 18 May 2014

Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4Structural and ligand binding properties of the Bateman domain of human magnesium transporters CNNM2 and CNNM4

Structural highlights

4iy3 is a 4 chain structure with sequence from Human. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Related:4iy0, 4iy2, 4iy4
Gene:CNNM4 (HUMAN)
Resources:FirstGlance, OCA, RCSB, PDBsum

Disease

[CNNM4_HUMAN] Jalili syndrome. The disease is caused by mutations affecting the gene represented in this entry.

Function

[CNNM4_HUMAN] Probable metal transporter. The interaction with the metal ion chaperone COX11 suggests that it may play a role in sensory neuron functions (By similarity). May play a role in biomineralization and retinal function.[1] [2]

References

  1. ↑ Polok B, Escher P, Ambresin A, Chouery E, Bolay S, Meunier I, Nan F, Hamel C, Munier FL, Thilo B, Megarbane A, Schorderet DF. Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta. Am J Hum Genet. 2009 Feb;84(2):259-65. doi: 10.1016/j.ajhg.2009.01.006. Epub 2009, Feb 5. PMID:19200527 doi:http://dx.doi.org/10.1016/j.ajhg.2009.01.006
  2. ↑ Parry DA, Mighell AJ, El-Sayed W, Shore RC, Jalili IK, Dollfus H, Bloch-Zupan A, Carlos R, Carr IM, Downey LM, Blain KM, Mansfield DC, Shahrabi M, Heidari M, Aref P, Abbasi M, Michaelides M, Moore AT, Kirkham J, Inglehearn CF. Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. Am J Hum Genet. 2009 Feb;84(2):266-73. doi: 10.1016/j.ajhg.2009.01.009. Epub 2009, Feb 5. PMID:19200525 doi:http://dx.doi.org/10.1016/j.ajhg.2009.01.009

4iy3, resolution 3.60Å

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