3zoz: Difference between revisions

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-'''Unreleased structure'''
+{{STRUCTURE_3zoz|  PDB=3zoz  |  SCENE=  }}
+===The structure of human phosphoglycerate kinase with bound bromide, a stimulating anion.===
-The entry 3zoz is ON HOLD  until Paper Publication
+==Disease==
+[[http://www.uniprot.org/uniprot/PGK1_HUMAN PGK1_HUMAN]] Defects in PGK1 are the cause of phosphoglycerate kinase 1 deficiency (PGK1D) [MIM:[http://omim.org/entry/300653 300653]]. It is a condition with a highly variable clinical phenotype that includes hemolytic anemia, rhabdomyolysis, myopathy and neurologic involvement. Patients can express one or more of these manifestations.<ref>PMID:8673469</ref> <ref>PMID:8043870</ref> <ref>PMID:8615693</ref> <ref>PMID:9744480</ref> <ref>PMID:2001457</ref> <ref>PMID:1586722</ref> <ref>PMID:1547346</ref> <ref>PMID:6941312</ref> <ref>PMID:6933565</ref>
-Authors: Bowler, M.W.
+==Function==
+[[http://www.uniprot.org/uniprot/PGK1_HUMAN PGK1_HUMAN]] In addition to its role as a glycolytic enzyme, it seems that PGK-1 acts as a polymerase alpha cofactor protein (primer recognition protein).
-Description: The structure of human phosphoglycerate kinase with bound bromide, a stimulating anion.
+==About this Structure==
+[[3zoz]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3ZOZ OCA].
+==Reference==
+<references group="xtra"/><references/>
+[[Category: Phosphoglycerate kinase]]
+[[Category: Bowler, M W.]]
+[[Category: Allosteric]]
+[[Category: Anion stimulation]]
+[[Category: Phosphoryl transfer]]
+[[Category: Transferase]]