about
Potential anti-bacterial drug target: structural characterization of 3,4-dihydroxy-2-butanone-4-phosphate synthase from Salmonella typhimurium LT2Crystal structure analysis of icosahedral lumazine synthase from Salmonella typhimurium, an antibacterial drug targetStructural insight into the inactivation of Mycobacterium tuberculosis non-classical transpeptidase LdtMt2 by biapenem and tebipenem.Non-classical transpeptidases yield insight into new antibacterialsRole of a non-canonical surface of Rad6 in ubiquitin conjugating activity.LdtMav2, a nonclassical transpeptidase and susceptibility of Mycobacterium avium to carbapenems.Mutation in an Unannotated Protein Confers Carbapenem Resistance in Mycobacterium tuberculosis.Inhibition of innate immune cytosolic surveillance by an M. tuberculosis phosphodiesterase.Structure of the yeast Bre1 RING domain.The crystal structure reveals the molecular mechanism of bifunctional 3,4-dihydroxy-2-butanone 4-phosphate synthase/GTP cyclohydrolase II (Rv1415) from Mycobacterium tuberculosis.Mycobacterium abscessus l,d-Transpeptidases Are Susceptible to Inactivation by Carbapenems and Cephalosporins but Not Penicillins.
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P50
description
researcher ORCID ID = 0000-0001-8650-5250
@en
name
Pankaj Kumar
@ast
Pankaj Kumar
@en
Pankaj Kumar
@es
Pankaj Kumar
@nl
type
label
Pankaj Kumar
@ast
Pankaj Kumar
@en
Pankaj Kumar
@es
Pankaj Kumar
@nl
prefLabel
Pankaj Kumar
@ast
Pankaj Kumar
@en
Pankaj Kumar
@es
Pankaj Kumar
@nl
P31
P496
0000-0001-8650-5250