4f9o

<StructureSection load='4f9o' size='340' side='right'caption='[[4f9o]], [[Resolution|resolution]] 2.65&Aring;' scene=''>

<table><tr><td colspan='2'>[[4f9o]] is a 2 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=4F9O OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4F9O FirstGlance]. <br>

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><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='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4f9o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4f9o OCA], [https://pdbe.org/4f9o PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4f9o RCSB], [https://www.ebi.ac.uk/pdbsum/4f9o PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4f9o ProSAT]</span></td></tr>

[https://www.uniprot.org/uniprot/HXK1_HUMAN HXK1_HUMAN] Defects in HK1 are the cause of hexokinase deficiency (HK deficiency) [MIM:[https://omim.org/entry/235700 235700]. HK deficiency is a rare autosomal recessive disease with nonspherocytic hemolytic anemia as the predominant clinical feature.

*[[Hexokinase 3D structures|Hexokinase 3D structures]]

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Honzatko RB]]

[[Category: Shen L]]