Function 
Glycerol kinase (GK) phosphorylates glycerol forming glycerol 3-phosphate (G3P) using Mg-ATP as phosphate source.   GK is a key enzyme in glycerol uptake and metabolism.  Mutations of GK gene cause GK deficiency syndrome.  PK is a multi-subunit allosteric enzyme.  Its activity can be inhibited by fructose 1,6-bisphosphate (FBP) and by the glucose-specific phosphocarrier IIA(Glc).  PK cofactor is a Zn atom which binds to the dimer[1].
  Disease 
GK Deficiency is an X-linked disease which has 3 forms: infantile, juvenile and adult[2]
  Structural highlights 
 is located in a cleft between two domains[3].