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Volumn 3, Issue 3, 2004, Pages 221-231

Inhibitors of mycothiol-S-conjugate amidase and related genes

Author keywords

Antituberculars; Marine natural products; Mycobacterium smegmatis; Myobacterium tuberculosis; Structural studies; Substrate based inhibitors

Indexed keywords

ACETYLCYSTEINE; AMIDASE; AMIDE; DISULFIDE; ENZYME INHIBITOR; ERYTHROMYCIN; GLIOTOXIN; GLUCOPYRANOSIDE; GLUCOSAMINE; GLUCOSAMINE DERIVATIVE; GLYCOSPHINGOLIPID; HALIFULFATE; INOSITOL; ISOXAZOLINE DERIVATIVE; OCEANAPISIDE; OCEANAPISIDE AGLYCON; PENICILLIN G; PHYSCION; PSAMMAPLIN DERIVATIVE; PSAMMAPLYSIN A; PSAMMAPLYSIN B; PYRIDINIUM DERIVATIVE; RIFAMPICIN; RIFAMYCIN; SESTERTERPENE; SUVANINE; THIOGLYCOSIDE; THIOL; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 4344601606     PISSN: 15680126     EISSN: None     Source Type: Journal    
DOI: 10.2174/1568012043353865     Document Type: Review
Times cited : (6)

References (59)
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  • 2
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    • WHO Fact Sheet No. 104, August
    • WHO Fact Sheet No. 104, August 2002.
    • (2002)
  • 3
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    • For additional information, see and http://www,who.int/health⊤pics/tuberculosis/en/
    • For additional information, see http://www.tballiance.org/ and http://www,who.int/health⊤pics/tuberculosis/en/.
  • 5
    • 0003881692 scopus 로고    scopus 로고
    • What is Dots? A Guide to Understanding the WHO-recommended TB Control Strategy Known as DOTS
    • World Health Organization. WHO/CDS/CPC/TB/99.270. Geneva, Switzerland: World Health Organization
    • World Health Organization. What is Dots? A Guide to Understanding the WHO-recommended TB Control Strategy Known as DOTS. WHO Report 1999: WHO/CDS/CPC/TB/99.270. Geneva, Switzerland: World Health Organization, 1999.
    • (1999) WHO Report 1999
  • 49
    • 0042123525 scopus 로고    scopus 로고
    • Although lacking any sequence homology to TT1542, MCA or other homologs, the recent MMR and X-ray structures of the metalloenzyme LpxC, which also hydrolyzes the C2 amide bond or glucosamine during biosynthesis of lipid A, reatures three histidines and one aspartate in the active site. See
    • Although lacking any sequence homology to TT1542, MCA or other homologs, the recent MMR and X-ray structures of the metalloenzyme LpxC, which also hydrolyzes the C2 amide bond or glucosamine during biosynthesis of lipid A, reatures three histidines and one aspartate in the active site. See Coggins B. E., Li, X.; McClerren, A. L.; Hindsgaul, O.; Raetz, C. R. H.; Zhou, P. Nature Struc. Biol. 2003, 10, 645;
    • (2003) Nature Struc. Biol. , vol.10 , pp. 645
    • Coggins, B.E.1    Li, X.2    McClerren, A.L.3    Hindsgaul, O.4    Raetz, C.R.H.5    Zhou, P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.