Authors: HONG L HARTSUCK JA FOUNDLING S ERMOLIEFF J TANG J

Citation: L. Hong et al., ACTIVE-SITE MOBILITY IN HUMAN-IMMUNODEFICIENCY-VIRUS, TYPE-1, PROTEASE AS DEMONSTRATED BY CRYSTAL-STRUCTURE OF A28S MUTANT, Protein science, 7(2), 1998, pp. 300-305

Authors: HONG L ZHANG XJ FOUNDLING S HARTSUCK JA TANG J

Citation: L. Hong et al., STRUCTURE OF A G48H MUTANT OF HIV-1 PROTEASE EXPLAINS HOW GLYCINE-48 REPLACEMENTS PRODUCE MUTANTS RESISTANT TO INHIBITOR DRUGS, FEBS letters, 420(1), 1997, pp. 11-16

Authors: HONG L TREHARNE A HARTSUCK JA FOUNDLING S TANG J

Citation: L. Hong et al., CRYSTAL-STRUCTURES OF COMPLEXES OF A PEPTIDIC INHIBITOR WITH WILD-TYPE AND 2 MUTANT HIV-1 PROTEASES, Biochemistry, 35(33), 1996, pp. 10627-10633

Authors: HONG L HARTSUCK JA TANG J TREHARNE A FOUNDLING S

Citation: L. Hong et al., CRYSTALLOGRAPHIC STUDY OF HIV PROTEASE RESISTANCE TO INHIBITORS, The FASEB journal, 9(6), 1995, pp. 1343-1343

Authors: TANG J HARTSUCK JA

Citation: J. Tang et Ja. Hartsuck, A KINETIC-MODEL FOR COMPARING PROTEOLYTIC PROCESSING ACTIVITY AND INHIBITOR RESISTANCE POTENTIAL OF MUTANT HIV-1 PROTEASES, FEBS letters, 367(2), 1995, pp. 112-116

Authors: CO E KOELSCH G LIN YZ IDO E HARTSUCK JA TANG J

Citation: E. Co et al., PROTEOLYTIC PROCESSING MECHANISMS OF A MINIPRECURSOR OF THE ASPARTIC PROTEASE OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1, Biochemistry, 33(5), 1994, pp. 1248-1254