58 related articles for article (PubMed ID: 1480035)
1. Inhibition of human skin fibroblast collagenase by phosphorus-containing peptides.
Galardy RE; Grobelny D; Kortylewicz ZP; Poncz L
Matrix Suppl; 1992; 1():259-62. PubMed ID: 1480035
[TBL] [Abstract][Full Text] [Related]
2. Inhibition of human skin fibroblast collagenase, thermolysin, and Pseudomonas aeruginosa elastase by peptide hydroxamic acids.
Grobelny D; Poncz L; Galardy RE
Biochemistry; 1992 Aug; 31(31):7152-4. PubMed ID: 1322694
[TBL] [Abstract][Full Text] [Related]
3. A new class of potent reversible inhibitors of metallo-proteinases: C-terminal thiol-peptides as zinc-coordinating ligands.
Peters K; Jahreis G; Kotters EM
J Enzyme Inhib; 2001 Oct; 16(4):339-50. PubMed ID: 11916139
[TBL] [Abstract][Full Text] [Related]
4. Purification and characterization of a neutral zinc endopeptidase secreted by Flavobacterium meningosepticum.
Grimwood BG; Plummer TH; Tarentino AL
Arch Biochem Biophys; 1994 May; 311(1):127-32. PubMed ID: 8185308
[TBL] [Abstract][Full Text] [Related]
5. Inhibition of matrix metalloproteinases by peptidyl hydroxamic acids.
Odake S; Morita Y; Morikawa T; Yoshida N; Hori H; Nagai Y
Biochem Biophys Res Commun; 1994 Mar; 199(3):1442-6. PubMed ID: 8147888
[TBL] [Abstract][Full Text] [Related]
6. Inactivation of human fibroblast collagenase by chloroacetyl N-hydroxypeptide derivatives.
Lin TY; Kuo DW
J Enzyme Inhib; 1991; 5(1):33-40. PubMed ID: 1669436
[TBL] [Abstract][Full Text] [Related]
7. Inhibition of human fibroblast collagenase by phthaloyl-glycylP-isoleucyl-tryptophan benzylamide (PP607).
Lin TY; Kuo D; Chang B; Walakovits L; Lark MW
Matrix Suppl; 1992; 1():311-2. PubMed ID: 1480045
[No Abstract] [Full Text] [Related]
8. 1.56 A structure of mature truncated human fibroblast collagenase.
Spurlino JC; Smallwood AM; Carlton DD; Banks TM; Vavra KJ; Johnson JS; Cook ER; Falvo J; Wahl RC; Pulvino TA
Proteins; 1994 Jun; 19(2):98-109. PubMed ID: 8090713
[TBL] [Abstract][Full Text] [Related]
9. An internally quenched fluorescent substrate for collagenase.
Saikumari YK; Balaram P
Biopolymers; 2008; 90(2):131-7. PubMed ID: 18260138
[TBL] [Abstract][Full Text] [Related]
10. Inhibition of bacterial collagenase by phosphonamide peptides.
Dive V; Nikolaou A; Yioatakis A; Labadie J; Toma F
Matrix Suppl; 1992; 1():136-7. PubMed ID: 1480014
[No Abstract] [Full Text] [Related]
11. Interaction of peptide substrates of fibroblast collagenase with divalent cations: Ca2+ binding by substrate as a suggested recognition signal for collagenase action.
Upadhye S; Ananthanarayanan VS
Biochem Biophys Res Commun; 1995 Oct; 215(2):474-82. PubMed ID: 7487980
[TBL] [Abstract][Full Text] [Related]
12. Inhibition of human stromelysin by peptides based on the N-terminal domain of tissue inhibitor of metalloproteinases-1.
Hanglow AC; Lugo A; Walsky R; Visnick M; Coffey JW; Fotouhi N
Biochem Biophys Res Commun; 1994 Dec; 205(2):1156-63. PubMed ID: 7802645
[TBL] [Abstract][Full Text] [Related]
13. Potent cyclic monomeric and dimeric peptide inhibitors of VLA-4 (alpha4beta1 integrin)-mediated cell adhesion based on the Ile-Leu-Asp-Val tetrapeptide.
Dutta AS; Crowther M; Gormley JJ; Hassall L; Hayward CF; Gellert PR; Kittlety RS; Alcock PJ; Jamieson A; Moores JM; Rees A; Wood LJ; Reilly CF; Haworth D
J Pept Sci; 2000 Jul; 6(7):321-41. PubMed ID: 10946997
[TBL] [Abstract][Full Text] [Related]
14. [Inhibition of the binding and activation of the first component of human complement. The effect of synthetic peptides, immunoglobulin fragments and various proteins].
Kozlov LV; Sizoĭ MN; Zinchenko AA; Levkovskiĭ AV
Biokhimiia; 1986 May; 51(5):707-18. PubMed ID: 3486677
[TBL] [Abstract][Full Text] [Related]
15. Sequence specificities of human fibroblast and neutrophil collagenases.
Netzel-Arnett S; Fields GB; Birkedal-Hansen H; Van Wart HE
J Biol Chem; 1991 Apr; 266(11):6747-55. PubMed ID: 1849891
[TBL] [Abstract][Full Text] [Related]
16. Slow- and fast-binding inhibitors of thermolysin display different modes of binding: crystallographic analysis of extended phosphonamidate transition-state analogues.
Holden HM; Tronrud DE; Monzingo AF; Weaver LH; Matthews BW
Biochemistry; 1987 Dec; 26(26):8542-53. PubMed ID: 3442675
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The most potent organophosphorus inhibitors of leucine aminopeptidase. Structure-based design, chemistry, and activity.
Grembecka J; Mucha A; Cierpicki T; Kafarski P
J Med Chem; 2003 Jun; 46(13):2641-55. PubMed ID: 12801228
[TBL] [Abstract][Full Text] [Related]
19. Bradykinin analogs as inhibitors of angiotensin-converting enzyme.
Chaturvedi D; Huelar E; Gunthorpe M; Gofman M; Krapf DS; Apostol E; Lewis WS
Pept Res; 1993; 6(6):308-12. PubMed ID: 8292848
[TBL] [Abstract][Full Text] [Related]
20. Inhibition of Clostridium histolyticum collagenases by phosphonamide peptide inhibitors.
Dive V; Yiotakis A; Nicolaou A; Toma F
Eur J Biochem; 1990 Aug; 191(3):685-93. PubMed ID: 2167850
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]