Yagami, T <br/><br/>
Adenosine di-, tri- and tetraphosphopyridoxals modify the same lysyl residue at the ATP-binding site in adenylate kinase.  [electronic resource] 

 -  FEBS letters  Mar 1988 
 - 261-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0014-5793 
<br/><br/><label>Standard No.: </label>10.1016/0014-5793(88)81137-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenine Nucleotides--pharmacology<br/>Adenosine Diphosphate--analogs & derivatives<br/>Adenosine Triphosphate--analogs & derivatives<br/>Adenylate Kinase--antagonists & inhibitors<br/>Amino Acids--analysis<br/>Animals<br/>Binding Sites<br/>Kinetics<br/>Muscles--enzymology<br/>Peptide Fragments--analysis<br/>Phosphotransferases--antagonists & inhibitors<br/>Protein Binding<br/>Pyridoxal--analogs & derivatives<br/>Pyridoxal Phosphate--analogs & derivatives<br/>Rabbits