Two crystal structures of human ornithine transcarbamylase (OTCase) complexed with the substrate carbamoyl phosphate (CP) have been solved. One structure, whose crystals were prepared by substituting N-phosphonacetyl--ornithine (PALO) liganded crystals with CP, has been refined at 2.4 A / (1 A / l 0.1 nm) resolution to a crystallographic R factor of 18.4 %. The second structure, whose crystals were prepared by co-crystallization with CP, has been refined at 2.6 A / resolution to a crystallographic R factor of 20.2 %. These structures provide important new insights into substrate recognition and ligandinduced conformational changes. Comparison of these structures with the structures of OTCase complexed with the bisubstrate