This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
4fpa
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | + | {{STRUCTURE_4fpa| PDB=4fpa | SCENE= }} | |
| + | ===Crystal Structure of recombinant human Hexokinase type I mutant D413N Glucose 6-Phosphate=== | ||
| - | + | ==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== | |
| - | + | [[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]. | |
| - | + | [[Category: Hexokinase]] | |
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Honzatko, R B.]] | ||
| + | [[Category: Shen, L.]] | ||
| + | [[Category: Glucose-6-phosphate]] | ||
| + | [[Category: Hexokinase]] | ||
| + | [[Category: Transferase]] | ||
Revision as of 14:15, 3 July 2013
Crystal Structure of recombinant human Hexokinase type I mutant D413N 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
4fpa is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
