4foi: Difference between revisions
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{{STRUCTURE_4foi| PDB=4foi | SCENE= }} | |||
===Crystal Structure of recombinant human Hexokinase type I mutant D413N with Glucose 1,6-bisphosphate=== | |||
==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. | |||
==About this Structure== | |||
[[4foi]] 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=4FOI OCA]. | |||
[[Category: Hexokinase]] | |||
[[Category: Homo sapiens]] | |||
[[Category: Honzatko, R B.]] | |||
[[Category: Shen, L.]] | |||
[[Category: 6-bisphosphate]] | |||
[[Category: Glucose 1]] | |||
[[Category: Hexokinase]] | |||
[[Category: Transferase]] | |||
Revision as of 14:15, 3 July 2013
Crystal Structure of recombinant human Hexokinase type I mutant D413N with Glucose 1,6-bisphosphate
Disease
[HXK1_HUMAN] Defects in HK1 are the cause of hexokinase deficiency (HK deficiency) [MIM:235700]. HK deficiency is a rare autosomal recessive disease with nonspherocytic hemolytic anemia as the predominant clinical feature.
About this Structure
4foi is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
