201 results on '"Bashiri, Ghader"'
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2. F420-dependent transformations in biosynthesis of secondary metabolites
3. DprE2 is a molecular target of the anti-tubercular nitroimidazole compounds pretomanid and delamanid
4. AvmM catalyses macrocyclization through dehydration/Michael-type addition in alchivemycin A biosynthesis
5. Flavin-enabled reductive and oxidative epoxide ring opening reactions
6. -NAD as a building block in natural product biosynthesis
7. β-NAD as a building block in natural product biosynthesis
8. F420-dependent glucose-6-phosphate dehydrogenase: A comprehensive review
9. Iran: a biochemist on torment and hope
10. Mechanistic insights into F420-dependent glucose-6-phosphate dehydrogenase using isotope effects and substrate inhibition studies
11. Abstract 1821 Investigating the catalytic mechanism of F420-dependent glucose-6-phosphate dehydrogenase through kinetic and thermodynamic analyses
12. Abstract 1445 Kinetic Studies on the catalytic mechanism of F420-dependent glucose-6-phosphate dehydrogenase
13. Abstract 1398 A very cool and novel phosphofructokinase sheds light on the evolution of substrate specificity and on the metabolic networks in our closest prokaryotic relatives
14. Mycobacterium tuberculosis Rv1916 is an Acetyl‐CoA‐Binding Protein
15. Targeting isocitrate lyase for the treatment of latent tuberculosis
16. Acetyl-CoA-mediated activation of Mycobacterium tuberculosis isocitrate lyase 2
17. Allosteric inhibition of Staphylococcus aureus MenD by 1,4-dihydroxy naphthoic acid: a feedback inhibition mechanism of the menaquinone biosynthesis pathway
18. Abstract 2214: Evidence of a Catalytic Dyad in F420-Dependent Glucose-6-Phosphate Dehydrogenase Using Steady-State and Pre Steady-State Kinetic Methods
19. A NADH-accepting imine reductase variant: Immobilization and cofactor regeneration by oxidative deamination
20. A revised biosynthetic pathway for the cofactor F420 in prokaryotes
21. Regulation and Quality Control of Adiponectin Assembly by Endoplasmic Reticulum Chaperone ERp44
22. A functional role of Rv1738 in Mycobacterium tuberculosis persistence suggested by racemic protein crystallography
23. Allosteric inhibition of Staphylococcus aureus MenD by 1,4-dihydroxy naphthoic acid: A feedback inhibition mechanism of the menaquinone biosynthesis pathway
24. Supplemental Material for 'Allosteric inhibition of Staphylococcus aureus MenD by 1,4-dihydroxy naphthoic acid: A feedback inhibition mechanism of the menaquinone biosynthesis pathway'
25. Cofactor F420, an emerging redox power in biosynthesis of secondary metabolites
26. Clusterin is involved in mediating the metabolic function of adipose SIRT1
27. Lipid transport across the mycobacterial cell envelope
28. Production of recombinant proteins in Mycobacterium smegmatis for structural and functional studies
29. Crystallographic Studies of F 420 ‐dependent Glucose‐6‐phosphate Dehydrogenase from M. tuberculosis
30. Accumulation of F 420 Cofactor‐based Intermediates within F 420 ‐Dependent Glucose‐6‐Phosphate Dehydrogenase using pH Dependence Profiling, Pre‐Steady State Kinetics and Global Analysis
31. Mechanistic studies on F 420 ‐dependent glucose‐6‐phosphate dehydrogenase using kinetic isotope effect methods and pH profiles
32. Redox Modifications in the Biosynthesis of Alchivemycin A Enable the Formation of Its Key Pharmacophore
33. Discovery and biosynthesis of guanipiperazine from a NRPS-like pathway
34. Itaconate is a covalent inhibitor of the Mycobacterium tuberculosis isocitrate lyase
35. Development of NMR and thermal shift assays for the evaluation of Mycobacterium tuberculosis isocitrate lyase inhibitors† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7md00456g
36. Mutations in fbiD ( Rv2983 ) as a Novel Determinant of Resistance to Pretomanid and Delamanid in Mycobacterium tuberculosis
37. Convergent pathways to biosynthesis of the versatile cofactor F420
38. Cofactor F420, an emerging redox power in biosynthesis of secondary metabolites.
39. Functional Genome Mining Reveals a Class V Lanthipeptide Containing ad‐Amino Acid Introduced by an F420H2‐Dependent Reductase
40. Allosteric regulation of menaquinone (vitamin K2) biosynthesis in the human pathogen Mycobacterium tuberculosis
41. Different Reaction Specificities of F420H2-Dependent Reductases Facilitate Pyrrolobenzodiazepines and Lincomycin To Fit Their Biological Targets
42. Allosteric Regulation of Vitamin K2 Biosynthesis in a Human Pathogen
43. The active site of the Mycobacterium tuberculosis branched-chain amino acid biosynthesis enzyme dihydroxyacid dehydratase contains a 2Fe–2S cluster
44. A revised biosynthetic pathway for the cofactor F420in bacteria
45. Mutations in Rv2983 as a novel determinant of resistance to nitroimidazole drugs in Mycobacterium tuberculosis
46. Functional Genome Mining Reveals a Class V Lanthipeptide Containing a d‐Amino Acid Introduced by an F420H2‐Dependent Reductase.
47. Allosteric regulation of menaquinone (vitamin K2) biosynthesis in the human pathogen Mycobacterium tuberculosis.
48. Biosynthesis of the Thiopeptins and Identification of an F420H2-Dependent Dehydropiperidine Reductase
49. Determining the active site base and order of substrate addition within F 420 ‐dependent glucose‐6‐phosphate using steady‐state and pre steady‐state kinetics and isotope effects methods
50. Mechanistic insights into F 420 -dependent glucose-6-phosphate dehydrogenase using isotope effects and substrate inhibition studies
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