Lau E P, Haley B E, Barden R E
Biochemistry. 1977 Jun 14;16(12):2581-5. doi: 10.1021/bi00631a001.
A photolabile reagent, p-azidobenzoyl-CoA, has been synthesized and tested as a photoaffinity label for acyl-CoA:glycine N-acyltransferase (EC 2.3.1.13) from beef liver. p-Azidobenzoyl-CoA is an active-site-directed reagent for this N-acyltransferase, since it is an alternate substrate (Km = 26 micronM, when [glycine] = 100 mM). Ultraviolet irradiation of a mixture of p-azidobenzoyl-CoA and the N-acyltransferase produces irreversible inhibition. Benzoyl-CoA protects the enzyme from inhibition by photoactivated p-azidobenzoyl-CoA. Acyl-CoA:glycine N-acyltransferase is composed of a single polypeptide with a molecular weight of about 35 000. Photolabeling experiments show that there is one active site per molecule of enzyme.
一种光不稳定试剂,对叠氮苯甲酰辅酶A,已被合成并作为来自牛肝的酰基辅酶A:甘氨酸N - 酰基转移酶(EC 2.3.1.13)的光亲和标记物进行了测试。对叠氮苯甲酰辅酶A是这种N - 酰基转移酶的活性位点导向试剂,因为它是一种替代底物(当[甘氨酸] = 100 mM时,Km = 26 μM)。对叠氮苯甲酰辅酶A和N - 酰基转移酶混合物的紫外线照射会产生不可逆抑制。苯甲酰辅酶A可保护该酶免受光活化的对叠氮苯甲酰辅酶A的抑制。酰基辅酶A:甘氨酸N - 酰基转移酶由一条分子量约为35000的单一多肽组成。光标记实验表明,每个酶分子有一个活性位点。