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4FF6

Mycobacterium tuberculosis DprE1 in complex with CT325 - monoclinic crystal form

Summary for 4FF6
Entry DOI10.2210/pdb4ff6/pdb
Related4FDN 4FDO 4FDP 4FEH
DescriptorProbable decaprenylphosphoryl-beta-D-ribose oxidase, FLAVIN-ADENINE DINUCLEOTIDE, 3-(hydroxyamino)-N-[(1R)-1-phenylethyl]-5-(trifluoromethyl)benzamide, ... (5 entities in total)
Functional Keywordsalpha+beta, oxidoreductase, decaprenylphosphoryl-beta-d-ribose, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor
Biological sourceMycobacterium tuberculosis
Total number of polymer chains2
Total formula weight107209.62
Authors
Batt, S.M.,Besra, G.S.,Futterer, K. (deposition date: 2012-05-31, release date: 2012-07-04, Last modification date: 2023-09-13)
Primary citationBatt, S.M.,Jabeen, T.,Bhowruth, V.,Quill, L.,Lund, P.A.,Eggeling, L.,Alderwick, L.J.,Futterer, K.,Besra, G.S.
Structural basis of inhibition of Mycobacterium tuberculosis DprE1 by benzothiazinone inhibitors.
Proc.Natl.Acad.Sci.USA, 109:11354-11359, 2012
Cited by
PubMed: 22733761
DOI: 10.1073/pnas.1205735109
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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