6q90
From Proteopedia
(Difference between revisions)
m (Protected "6q90" [edit=sysop:move=sysop]) |
|||
Line 1: | Line 1: | ||
- | '''Unreleased structure''' | ||
- | + | ==Structure of human galactokinase 1 bound with 1-(4-Methoxyphenyl)-3-(4-pyridinyl)urea== | |
+ | <StructureSection load='6q90' size='340' side='right'caption='[[6q90]], [[Resolution|resolution]] 2.40Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[6q90]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6Q90 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6Q90 FirstGlance]. <br> | ||
+ | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.4Å</td></tr> | ||
+ | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GAL:BETA-D-GALACTOSE'>GAL</scene>, <scene name='pdbligand=HFK:2-(1,3-benzoxazol-2-ylamino)spiro[1,6,7,8-tetrahydroquinazoline-4,1-cyclohexane]-5-one'>HFK</scene>, <scene name='pdbligand=JHJ:N-(4-methoxyphenyl)-N-pyridin-4-ylurea'>JHJ</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=6q90 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6q90 OCA], [https://pdbe.org/6q90 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6q90 RCSB], [https://www.ebi.ac.uk/pdbsum/6q90 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6q90 ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Disease == | ||
+ | [https://www.uniprot.org/uniprot/GALK1_HUMAN GALK1_HUMAN] Defects in GALK1 are the cause of galactosemia II (GALCT2) [MIM:[https://omim.org/entry/230200 230200]. Galactosemia II is an autosomal recessive deficiency characterized by congenital cataracts during infancy and presenile cataracts in the adult population. The cataracts are secondary to accumulation of galactitol in the lenses.<ref>PMID:10521295</ref> <ref>PMID:10790206</ref> <ref>PMID:11231902</ref> <ref>PMID:11139256</ref> <ref>PMID:12694189</ref> <ref>PMID:15024738</ref> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/GALK1_HUMAN GALK1_HUMAN] Major enzyme for galactose metabolism. | ||
- | + | ==See Also== | |
- | + | *[[Galactokinase|Galactokinase]] | |
- | + | == References == | |
- | [[Category: | + | <references/> |
- | [[Category: | + | __TOC__ |
- | [[Category: | + | </StructureSection> |
- | [[Category: | + | [[Category: Homo sapiens]] |
- | [[Category: | + | [[Category: Large Structures]] |
- | [[Category: | + | [[Category: Arrowsmith C]] |
- | [[Category: | + | [[Category: Bezerra GA]] |
- | [[Category: | + | [[Category: Bountra C]] |
- | [[Category: Edwards | + | [[Category: Brandao-Neto J]] |
- | [[Category: | + | [[Category: Brennan P]] |
- | [[Category: | + | [[Category: Douangamath A]] |
- | [[Category: | + | [[Category: Edwards A]] |
- | [[Category: | + | [[Category: Foster W]] |
- | [[Category: | + | [[Category: Krojer T]] |
+ | [[Category: Lai K]] | ||
+ | [[Category: Mackinnon SR]] | ||
+ | [[Category: Yue WW]] | ||
+ | [[Category: Zhang M]] |
Revision as of 11:55, 24 January 2024
Structure of human galactokinase 1 bound with 1-(4-Methoxyphenyl)-3-(4-pyridinyl)urea
|
Categories: Homo sapiens | Large Structures | Arrowsmith C | Bezerra GA | Bountra C | Brandao-Neto J | Brennan P | Douangamath A | Edwards A | Foster W | Krojer T | Lai K | Mackinnon SR | Yue WW | Zhang M