6gr2
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Structure of human galactokinase in complex with galactose and ADP== | |
- | + | <StructureSection load='6gr2' size='340' side='right'caption='[[6gr2]], [[Resolution|resolution]] 2.49Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[6gr2]] is a 8 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6GR2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6GR2 FirstGlance]. <br> | |
- | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ADP:ADENOSINE-5-DIPHOSPHATE'>ADP</scene>, <scene name='pdbligand=GAL:BETA-D-GALACTOSE'>GAL</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | |
- | [[Category: | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1wuu|1wuu]]</td></tr> |
- | [[Category: | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Galactokinase Galactokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.6 2.7.1.6] </span></td></tr> |
+ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6gr2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6gr2 OCA], [http://pdbe.org/6gr2 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6gr2 RCSB], [http://www.ebi.ac.uk/pdbsum/6gr2 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6gr2 ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Disease == | ||
+ | [[http://www.uniprot.org/uniprot/GALK1_HUMAN GALK1_HUMAN]] Defects in GALK1 are the cause of galactosemia II (GALCT2) [MIM:[http://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 == | ||
+ | [[http://www.uniprot.org/uniprot/GALK1_HUMAN GALK1_HUMAN]] Major enzyme for galactose metabolism. | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Galactokinase]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Arrowsmith, C]] | ||
+ | [[Category: Bezerra, G A]] | ||
+ | [[Category: Bountra, C]] | ||
+ | [[Category: Edwards, A]] | ||
+ | [[Category: Lai, K]] | ||
[[Category: Mackinnon, S]] | [[Category: Mackinnon, S]] | ||
- | + | [[Category: Structural genomic]] | |
- | + | ||
- | [[Category: Structural | + | |
- | + | ||
[[Category: Williams, E]] | [[Category: Williams, E]] | ||
- | [[Category: Yue, W | + | [[Category: Yue, W W]] |
- | [[Category: | + | [[Category: Zhang, M]] |
- | [[Category: | + | [[Category: Adp]] |
+ | [[Category: Galactose]] | ||
+ | [[Category: Ghmp kinase]] | ||
+ | [[Category: Leloir pathway]] | ||
+ | [[Category: Sgc]] | ||
+ | [[Category: Transferase]] |
Revision as of 05:54, 19 June 2019
Structure of human galactokinase in complex with galactose and ADP
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Categories: Galactokinase | Large Structures | Arrowsmith, C | Bezerra, G A | Bountra, C | Edwards, A | Lai, K | Mackinnon, S | Structural genomic | Williams, E | Yue, W W | Zhang, M | Adp | Galactose | Ghmp kinase | Leloir pathway | Sgc | Transferase