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3. Possible role for water dissociation in the slow binding of phosphorus-containing transition-state-analogue inhibitors of thermolysin. Bartlett PA; Marlowe CK Biochemistry; 1987 Dec; 26(26):8553-61. PubMed ID: 3442676 [TBL] [Abstract][Full Text] [Related]
4. A theoretical investigation of tight-binding thermolysin inhibitors. Shen J J Med Chem; 1997 Aug; 40(18):2953-8. PubMed ID: 9288178 [TBL] [Abstract][Full Text] [Related]
5. Crystallographic structural analysis of phosphoramidates as inhibitors and transition-state analogs of thermolysin. Tronrud DE; Monzingo AF; Matthews BW Eur J Biochem; 1986 Jun; 157(2):261-8. PubMed ID: 3709536 [TBL] [Abstract][Full Text] [Related]
6. Binding of N-carboxymethyl dipeptide inhibitors to thermolysin determined by X-ray crystallography: a novel class of transition-state analogues for zinc peptidases. Monzingo AF; Matthews BW Biochemistry; 1984 Nov; 23(24):5724-9. PubMed ID: 6395881 [TBL] [Abstract][Full Text] [Related]
7. Evaluation of intrinsic binding energy from a hydrogen bonding group in an enzyme inhibitor. Bartlett PA; Marlowe CK Science; 1987 Jan; 235(4788):569-71. PubMed ID: 3810155 [TBL] [Abstract][Full Text] [Related]
9. The binding of L-valyl-L-tryptophan to crystalline thermolysin illustrates the mode of interaction of a product of peptide hydrolysis. Holden HM; Matthews BW J Biol Chem; 1988 Mar; 263(7):3256-60. PubMed ID: 3343246 [TBL] [Abstract][Full Text] [Related]
10. Phosphonate analogues of carboxypeptidase A substrates are potent transition-state analogue inhibitors. Hanson JE; Kaplan AP; Bartlett PA Biochemistry; 1989 Jul; 28(15):6294-305. PubMed ID: 2790000 [TBL] [Abstract][Full Text] [Related]
11. X-ray structures of human neutrophil collagenase complexed with peptide hydroxamate and peptide thiol inhibitors. Implications for substrate binding and rational drug design. Grams F; Reinemer P; Powers JC; Kleine T; Pieper M; Tschesche H; Huber R; Bode W Eur J Biochem; 1995 Mar; 228(3):830-41. PubMed ID: 7737183 [TBL] [Abstract][Full Text] [Related]
12. Structural analysis of silanediols as transition-state-analogue inhibitors of the benchmark metalloprotease thermolysin. Juers DH; Kim J; Matthews BW; Sieburth SM Biochemistry; 2005 Dec; 44(50):16524-8. PubMed ID: 16342943 [TBL] [Abstract][Full Text] [Related]
13. An interactive computer graphics study of thermolysin-catalyzed peptide cleavage and inhibition by N-carboxymethyl dipeptides. Hangauer DG; Monzingo AF; Matthews BW Biochemistry; 1984 Nov; 23(24):5730-41. PubMed ID: 6525336 [TBL] [Abstract][Full Text] [Related]
14. Binding of phosphorus-containing inhibitors to thermolysin studied by the Poisson-Boltzmann method. Shen J; Wendoloski J Protein Sci; 1995 Mar; 4(3):373-81. PubMed ID: 7795520 [TBL] [Abstract][Full Text] [Related]
15. Phosphonamidates as transition-state analogue inhibitors of thermolysin. Bartlett PA; Marlowe CK Biochemistry; 1983 Sep; 22(20):4618-24. PubMed ID: 6626519 [TBL] [Abstract][Full Text] [Related]
16. Binding energetics of phosphorus-containing inhibitors of thermolysin. Grobelny D; Goli UB; Galardy RE Biochemistry; 1989 Jun; 28(12):4948-51. PubMed ID: 2765520 [TBL] [Abstract][Full Text] [Related]
17. Structural basis for the action of thermolysin. Tronrud DE; Roderick SL; Matthews BW Matrix Suppl; 1992; 1():107-11. PubMed ID: 1480010 [TBL] [Abstract][Full Text] [Related]
18. Crystal structure of the complex of carboxypeptidase A with a strongly bound phosphonate in a new crystalline form: comparison with structures of other complexes. Kim H; Lipscomb WN Biochemistry; 1990 Jun; 29(23):5546-55. PubMed ID: 2386784 [TBL] [Abstract][Full Text] [Related]