4lrh: Difference between revisions
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==Crystal structure of human folate receptor alpha in complex with folic acid== | ==Crystal structure of human folate receptor alpha in complex with folic acid== | ||
<StructureSection load='4lrh' size='340' side='right' caption='[[4lrh]], [[Resolution|resolution]] 2.80Å' scene=''> | <StructureSection load='4lrh' size='340' side='right'caption='[[4lrh]], [[Resolution|resolution]] 2.80Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4lrh]] is a 8 chain structure with sequence from [ | <table><tr><td colspan='2'>[[4lrh]] is a 8 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=4keo 4keo]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LRH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4LRH FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=FOL:FOLIC+ACID'>FOL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FOL:FOLIC+ACID'>FOL</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4lrh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4lrh OCA], [https://pdbe.org/4lrh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4lrh RCSB], [https://www.ebi.ac.uk/pdbsum/4lrh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4lrh ProSAT]</span></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/FOLR1_HUMAN FOLR1_HUMAN] Neurodegenerative syndrome due to cerebral folate transport deficiency. Neurodegeneration due to cerebral folate transport deficiency (NCFTD) [MIM:[https://omim.org/entry/613068 613068]: A neurodegenerative disorder resulting from brain-specific folate deficiency early in life. Onset is apparent in late infancy with severe developmental regression, movement disturbances, epilepsy and leukodystrophy. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/FOLR1_HUMAN FOLR1_HUMAN] Binds to folate and reduced folic acid derivatives and mediates delivery of 5-methyltetrahydrofolate to the interior of cells. | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Brunzelle | [[Category: Large Structures]] | ||
[[Category: Chen | [[Category: Brunzelle JS]] | ||
[[Category: Ke | [[Category: Chen C]] | ||
[[Category: Li | [[Category: Ke J]] | ||
[[Category: Melcher | [[Category: Li J]] | ||
[[Category: Xu | [[Category: Melcher K]] | ||
[[Category: Yi | [[Category: Xu HE]] | ||
[[Category: Young | [[Category: Yi W]] | ||
[[Category: Zhou | [[Category: Young E-L]] | ||
[[Category: Zhou XE]] | |||