PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 12675602-9 2003 The most stable CPA-glyoxyl derivative could be efficiently used in the hydrolysis of long-chain peptides at high temperature (e.g., 60 degrees C), being able to release 2-fold more aromatic amino acids (Tyr, Phe, and Trp) than the soluble enzyme, under the same operational conditions. Phenylalanine 209-212 carboxypeptidase A1 Homo sapiens 16-19 3718539-2 1986 However, both CPB and CPA degraded the des-Arg derivatives to remove the C-terminal phenylalanine. Phenylalanine 84-97 carboxypeptidase A1 Homo sapiens 22-25 3718539-3 1986 The inhibitory effect of phosphate ions upon this activity of CPB (but not CPA) suggests that CPA may be responsible for the formation of free phenylalanine seen upon degradation of kinins in plasma or serum. Phenylalanine 143-156 carboxypeptidase A1 Homo sapiens 94-97 7082637-4 1982 The CPA-catalyzed hydrolysis of Z-Glys-Phe was shown to involve only C-N bond cleavage, to give carbobenzoxythioglycine and phenylalanine. Phenylalanine 124-137 carboxypeptidase A1 Homo sapiens 4-7 27841396-8 2016 However, for the substrate mutant that contains Asp instead of Phe at the C-terminus, one CPA mutant exhibits a reasonable activity, as predicted across the theoretical methods. Phenylalanine 63-66 carboxypeptidase A1 Homo sapiens 90-93 9840967-3 1998 BSA contains several electrostatic, hydrogen bonding and hydrophobic binding sites for potential interaction with the metal complexes, and CPA contains a specific phenylalanine binding site. Phenylalanine 163-176 carboxypeptidase A1 Homo sapiens 139-142 7834611-4 1995 When the lung tumor cells were treated with CPA conjugated to KS1/4 (a mAb targeted to these cells) and excess conjugate removed by extensive washing, the ID50 for MTX-Phe improved from 2.2 x 10(-6) M (no enzyme present) to 6.3 x 10(-8) M; the latter value was comparable to that of the parent drug MTX (4.5 x 10(-8) M). Phenylalanine 168-171 carboxypeptidase A1 Homo sapiens 44-47