4fpa: Difference between revisions

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'''Unreleased structure'''
{{STRUCTURE_4fpa|  PDB=4fpa  |  SCENE=  }}
===Crystal Structure of recombinant human Hexokinase type I mutant D413N Glucose 6-Phosphate===


The entry 4fpa is ON HOLD  until Paper Publication
==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.


Authors: Shen, L., Honzatko, R.B.
==About this Structure==
 
[[4fpa]] 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=4FPA OCA].  
Description: Crystal Structure of recombinant human Hexokinase type I mutant D413N Glucose 6-Phosphate
[[Category: Hexokinase]]
[[Category: Homo sapiens]]
[[Category: Honzatko, R B.]]
[[Category: Shen, L.]]
[[Category: Glucose-6-phosphate]]
[[Category: Hexokinase]]
[[Category: Transferase]]