4f9o

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'''Unreleased structure'''
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{{STRUCTURE_4f9o| PDB=4f9o | SCENE= }}
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===Crystal Structure of recombinant human Hexokinase type I with 2-deoxy-Glucose 6-Phosphate===
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The entry 4f9o is ON HOLD until Paper Publication
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==Disease==
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[[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.
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Authors: Shen, L., Honzatko, R.B.
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==About this Structure==
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[[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].
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Description: Crystal Structure of recombinant human Hexokinase type I with 2-deoxy-Glucose 6-Phosphate
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[[Category: Hexokinase]]
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[[Category: Homo sapiens]]
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[[Category: Honzatko, R B.]]
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[[Category: Shen, L.]]
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[[Category: 2-deoxy glucose-6-phosphate]]
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[[Category: Hexokinase]]
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[[Category: Transferase]]

Revision as of 21:02, 19 June 2013

Template:STRUCTURE 4f9o

Crystal Structure of recombinant human Hexokinase type I with 2-deoxy-Glucose 6-Phosphate

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

4f9o is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Proteopedia Page Contributors and Editors (what is this?)

OCA

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