4fpb: Difference between revisions

Revision as of 17:15, 3 July 2013

Crystal Structure of Recombinant Human Hexokinase Type I with 1,5-Anhydroglucitol 6-PhosphateCrystal Structure of Recombinant Human Hexokinase Type I with 1,5-Anhydroglucitol 6-Phosphate

DiseaseDisease

[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 StructureAbout this Structure

4fpb 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?)Proteopedia Page Contributors and Editors (what is this?)

OCA

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{STRUCTURE_4fpb|  PDB=4fpb  |  SCENE=  }}
+===Crystal Structure of Recombinant Human Hexokinase Type I with 1,5-Anhydroglucitol 6-Phosphate===
-The entry 4fpb 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==
+[[4fpb]] 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=4FPB OCA].
-Description: Crystal Structure of Recombinant Human Hexokinase Type I with 1,5-Anhydroglucitol 6-Phosphate
+[[Category: Hexokinase]]
+[[Category: Homo sapiens]]
+[[Category: Honzatko, R B.]]
+[[Category: Shen, L.]]
+[[Category: 5-anhydroglucitol 6-phosphate]]
+[[Category: Hexokinase]]
+[[Category: Transferase]]