4f9o
From Proteopedia
(Difference between revisions)
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| - | + | ==Crystal Structure of recombinant human Hexokinase type I with 2-deoxy-Glucose 6-Phosphate== | |
| - | + | <StructureSection load='4f9o' size='340' side='right' caption='[[4f9o]], [[Resolution|resolution]] 2.65Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | ==Disease== | + | <table><tr><td colspan='2'>[[4f9o]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4F9O OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4F9O FirstGlance]. <br> |
| + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=0NZ:2-DEOXY-6-O-PHOSPHONO-BETA-D-ARABINO-HEXOPYRANOSE'>0NZ</scene>, <scene name='pdbligand=BGC:BETA-D-GLUCOSE'>BGC</scene>, <scene name='pdbligand=CIT:CITRIC+ACID'>CIT</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr> | ||
| + | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">HK1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr> | ||
| + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Hexokinase Hexokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.1 2.7.1.1] </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=4f9o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4f9o OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4f9o RCSB], [http://www.ebi.ac.uk/pdbsum/4f9o PDBsum]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
[[http://www.uniprot.org/uniprot/HXK1_HUMAN HXK1_HUMAN]] Defects in HK1 are the cause of hexokinase deficiency (HK deficiency) [MIM:[http://omim.org/entry/235700 235700]]. HK deficiency is a rare autosomal recessive disease with nonspherocytic hemolytic anemia as the predominant clinical feature. | [[http://www.uniprot.org/uniprot/HXK1_HUMAN HXK1_HUMAN]] Defects in HK1 are the cause of hexokinase deficiency (HK deficiency) [MIM:[http://omim.org/entry/235700 235700]]. HK deficiency is a rare autosomal recessive disease with nonspherocytic hemolytic anemia as the predominant clinical feature. | ||
| + | == Function == | ||
| - | == | + | |
| - | [[ | + | ==See Also== |
| + | *[[Hexokinase|Hexokinase]] | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
[[Category: Hexokinase]] | [[Category: Hexokinase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Honzatko, R B | + | [[Category: Honzatko, R B]] |
| - | [[Category: Shen, L | + | [[Category: Shen, L]] |
[[Category: 2-deoxy glucose-6-phosphate]] | [[Category: 2-deoxy glucose-6-phosphate]] | ||
| - | [[Category: Hexokinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
Revision as of 11:43, 21 December 2014
Crystal Structure of recombinant human Hexokinase type I with 2-deoxy-Glucose 6-Phosphate
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