Preferred hydrolysis of methyl d-pyroglutamates (5-carbomethoxy-2-pyrrolidones) by α-chymotrypsin

Bioorganic Chemistry

Volumn 6, Issue 3, 1977, Pages 329-340

  Gillan, Thomas ^a   Mor, Gideon ^a   Pepper, Frederick W ^a   Cohen, Saul G ^a  

^a BRANDEIS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHYMOTRYPSIN A;

IN VITRO STUDY; PYROGLUTAMIC ACID METHYL ESTER; THEORETICAL STUDY;

EID: 0017378947     PISSN: 00452068     EISSN: 10902120     Source Type: Journal    
DOI: 10.1016/0045-2068(77)90033-5     Document Type: Article

References (34)

1. .alpha.-Chymotrypsin. Use of substrates of restricted geometry to define the reactive conformation of methyl N-acetyl-L-phenylalaninate
2. Structure and Substrate Specificity in the Serine Enzymes
3. THE ACTIVE SITE IN -CHYMOTRYPSIN: METHYL 3,4-DIHYDROISOCOUMARIN-3-CARBOXYLATE I
4. The Crystal Structure and the Absolute Configuration of (+)-2-Benzylglutamic Acid Hydrobromide Dihydrate