4fpb

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
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]]

Revision as of 14:15, 3 July 2013

Template:STRUCTURE 4fpb

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

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?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/4fpb"
Personal tools