메뉴 건너뛰기




Volumn 48, Issue 3, 2008, Pages 202-206

Peptide inhibitors of MurD and MurE, essential enzymes of bacterial cell wall biosynthesis

Author keywords

Cell wall biosynthesis; Mur ligase; Peptide inhibitor; Peptidoglycan; Phage display

Indexed keywords

BACTERIA (MICROORGANISMS);

EID: 47649112998     PISSN: 0233111X     EISSN: 15214028     Source Type: Journal    
DOI: 10.1002/jobm.200700133     Document Type: Article
Times cited : (22)

References (19)
  • 1
    • 0036791627 scopus 로고    scopus 로고
    • New (and not so new) antibacterial targets - from where and when will the novel drugs come?
    • Projan, S.J., 2002. New (and not so new) antibacterial targets - from where and when will the novel drugs come? Curr. Opin. Pharmacol., 2, 513-522.
    • (2002) Curr. Opin. Pharmacol , vol.2 , pp. 513-522
    • Projan, S.J.1
  • 2
    • 33947309695 scopus 로고    scopus 로고
    • Emerging bacterial enzyme targets
    • Su, Z. and Honek, J.F., 2007. Emerging bacterial enzyme targets. Curr. Opin. Invest. Drugs, 8(2), 140-149.
    • (2007) Curr. Opin. Invest. Drugs , vol.8 , Issue.2 , pp. 140-149
    • Su, Z.1    Honek, J.F.2
  • 3
    • 0142126675 scopus 로고    scopus 로고
    • Bacterial wall as target for attack: Past, present, and future research
    • Koch, A.L., 2003. Bacterial wall as target for attack: past, present, and future research. Clin. Microbiol. Rev., 16(4), 673-687.
    • (2003) Clin. Microbiol. Rev , vol.16 , Issue.4 , pp. 673-687
    • Koch, A.L.1
  • 4
    • 0035933529 scopus 로고    scopus 로고
    • Bernhardt, T.G., Wang, I.N., Struck and D.K., Young, R., 2001. A protein antibiotic in the phage Qbeta virion: diversity in lysis targets. Science, 292, 2326-2329.
    • Bernhardt, T.G., Wang, I.N., Struck and D.K., Young, R., 2001. A protein antibiotic in the phage Qbeta virion: diversity in lysis targets. Science, 292, 2326-2329.
  • 5
    • 0032428375 scopus 로고    scopus 로고
    • Selective inhibition of the bacterial peptidoglycan synthesis by the new types of liposidomycins
    • Kimura, K., Ikeda, Y., Kagami, S, Yoshihama, M. et al., 1998. Selective inhibition of the bacterial peptidoglycan synthesis by the new types of liposidomycins. J. Antibiot., 51, 1099-1104.
    • (1998) J. Antibiot , vol.51 , pp. 1099-1104
    • Kimura, K.1    Ikeda, Y.2    Kagami, S.3    Yoshihama, M.4
  • 6
    • 0037223505 scopus 로고    scopus 로고
    • Structure and function of the Mur enzymes: Development of novel inhibitors
    • El Zoeiby, A., Sanschagrin, F. and Levesque, R.C., 2003. Structure and function of the Mur enzymes: development of novel inhibitors. Mol. Microbiol., 47(1), 1-12.
    • (2003) Mol. Microbiol , vol.47 , Issue.1 , pp. 1-12
    • El Zoeiby, A.1    Sanschagrin, F.2    Levesque, R.C.3
  • 7
    • 0036480755 scopus 로고    scopus 로고
    • The bacterial cell wall as a source of antibacterial targets
    • Green, D.W., 2002. The bacterial cell wall as a source of antibacterial targets. Expert Opin. Ther. Targets, 6(1), 1-19.
    • (2002) Expert Opin. Ther. Targets , vol.6 , Issue.1 , pp. 1-19
    • Green, D.W.1
  • 8
    • 0037241238 scopus 로고    scopus 로고
    • Structure-based design approaches to cell wall biosynthesis inhibitors
    • Katz, A.H. and Caufield, C.E., 2003. Structure-based design approaches to cell wall biosynthesis inhibitors. Curr. Pharm. Des., 9, 857-866.
    • (2003) Curr. Pharm. Des , vol.9 , pp. 857-866
    • Katz, A.H.1    Caufield, C.E.2
  • 9
    • 33644558385 scopus 로고    scopus 로고
    • Does the cell wall of bacteria remain a viable source of targets for novel antibiotics?
    • Silver, L.L., 2006. Does the cell wall of bacteria remain a viable source of targets for novel antibiotics? Biochem. Pharmacol., 71, 996-1005.
    • (2006) Biochem. Pharmacol , vol.71 , pp. 996-1005
    • Silver, L.L.1
  • 10
    • 0037339206 scopus 로고    scopus 로고
    • Identification of novel inhibitors of Pseudomonas aeruginosa MurC enzyme derived from phage-displayed peptide libraries
    • El Zoeiby, A., Sanschagrin, F., Darveau, A., Brisson, J.-R. and Levesque, R.C., 2003. Identification of novel inhibitors of Pseudomonas aeruginosa MurC enzyme derived from phage-displayed peptide libraries. J. Antimicrob. Chemother., 51, 531-543.
    • (2003) J. Antimicrob. Chemother , vol.51 , pp. 531-543
    • El Zoeiby, A.1    Sanschagrin, F.2    Darveau, A.3    Brisson, J.-R.4    Levesque, R.C.5
  • 11
    • 33744983912 scopus 로고    scopus 로고
    • Selection of peptide inhibitors against the Pseudomonas aeruginosa MurD cell wall enzyme
    • Paradis-Bleau, C., Beaumont, M., Boudreault, L., Lloyd, A. et al., 2006. Selection of peptide inhibitors against the Pseudomonas aeruginosa MurD cell wall enzyme. Peptides, 27(7), 1693-1700.
    • (2006) Peptides , vol.27 , Issue.7 , pp. 1693-1700
    • Paradis-Bleau, C.1    Beaumont, M.2    Boudreault, L.3    Lloyd, A.4
  • 13
    • 33748324503 scopus 로고    scopus 로고
    • Structure, function and dynamics in the mur family of bacterial cell wall ligases
    • Smith, C.A., 2006. Structure, function and dynamics in the mur family of bacterial cell wall ligases. J. Mol. Biol., 362, 640-655.
    • (2006) J. Mol. Biol , vol.362 , pp. 640-655
    • Smith, C.A.1
  • 14
    • 0034283162 scopus 로고    scopus 로고
    • Open' structures of MurD: Domain movements and structural similarities with folylpolyglutamate synthetase
    • Bertrand, J.A., Fanchon, E., Martin, L., Chantalat, L. et al., 2000. 'Open' structures of MurD: Domain movements and structural similarities with folylpolyglutamate synthetase. J. Mol. Biol., 301, 1257-1266.
    • (2000) J. Mol. Biol , vol.301 , pp. 1257-1266
    • Bertrand, J.A.1    Fanchon, E.2    Martin, L.3    Chantalat, L.4
  • 16
    • 0030976150 scopus 로고    scopus 로고
    • Bacteriophage display and discovery of peptide leads for drug development
    • Lowman, H.B., 1997. Bacteriophage display and discovery of peptide leads for drug development. Annu. Rev. Biomol. Struct., 26, 401-424.
    • (1997) Annu. Rev. Biomol. Struct , vol.26 , pp. 401-424
    • Lowman, H.B.1
  • 17
    • 3543143166 scopus 로고    scopus 로고
    • Identification of Pseudomonas aeruginosa FtsZ peptide inhibitors as a tool for the development of novel antimicrobials
    • Paradis-Bleau, C., Sanschagrin, F. and Levesque, R.C., 2004. Identification of Pseudomonas aeruginosa FtsZ peptide inhibitors as a tool for the development of novel antimicrobials. J. Antimicrob. Chemother., 54(1), 278-280.
    • (2004) J. Antimicrob. Chemother , vol.54 , Issue.1 , pp. 278-280
    • Paradis-Bleau, C.1    Sanschagrin, F.2    Levesque, R.C.3
  • 18
    • 17644401295 scopus 로고    scopus 로고
    • Paradis-Bleau, C., Sanschagrin, F. and Levesque, R.C., 2005. Peptide inhibitors of the essential cell division protein FtsA. Protein Eng. Des. Select., 18(2), 85-91.
    • Paradis-Bleau, C., Sanschagrin, F. and Levesque, R.C., 2005. Peptide inhibitors of the essential cell division protein FtsA. Protein Eng. Des. Select., 18(2), 85-91.
  • 19


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.