151 results on '"Villeret V"'
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2. Crystal structure of the SARS-CoV-2 Main Protease complexed with N-(pyridin-3-ylmethyl)thioformamide
3. Crystallographic structure of human Tsg101 UEV domain in complex with a HEV ORF3 peptide
4. Crystal structure of the SARS-CoV-2 Main Protease
5. Crystal structure of the SARS-CoV-2 Main Protease with a Zinc ion coordinated in the active site
6. Crystal structure of the SARS-CoV-2 Main Protease with oxidized C145
7. Structure–based Mechanism of Ligand Binding for Periplasmic Solute-binding Protein of the Bug Family
8. Structure of the PAS domain from Bordetella pertussis BvgS
9. Crystal structure of human Mediator subunit MED23
10. HUMAN MED26 N-TERMINAL DOMAIN (1-92)
11. Human Med26 N-Terminal Domain (1-92)
12. Structure of a complex between hemopexin and hemopexin binding protein
13. Crystal structure of Hemopexin Binding Protein
14. The DivJ, CbrA and PleC system controls DivK phosphorylation and symbiosis in Sinorhizobium meliloti
15. Crystal Structure Analysis of the Membrane Transporter FhaC (double mutant V169T, I176N)
16. 3.1 A resolution crystal structure of the B. pertussis BvgS periplasmic domain
17. Crystal Structure Analysis of the Membrane Transporter FhaC
18. Rapid and efficient design of new inhibitors of Mycobacterium tuberculosis transcriptional repressor EthR using fragment growing, merging and linking approaches
19. Crystal structures of a psychrophilic metalloprotease reveal new insights into catalysis by cold-adapted proteases
20. The crystal structure of the Haemophilus influenzae HxuA secretion domain involved in the two-partner secretion pathway
21. Novel N-phenyl-phenoxyacetamide derivatives as potential EthR inhibitors and ethionamide boosters. Discovery and optimization using High-Throughput Synthesis.
22. Bacterial phosphotransferase
23. EthR from Mycobacterium tuberculosis in complex with compound BDM5683
24. ETHR From mycobacterium tuberculosis in complex with compound bdm31369
25. G106W mutant of EthR from Mycobacterium tuberculosis
26. Structural activation of the transcriptional repressor EthR from M. tuberculosis by single amino-acid change mimicking natural and synthetic ligands
27. ETHR From mycobacterium tuberculosis in complex with compound BDM33066
28. Ethionamide Boosters Part 2: Combining Bioisosteric Replacement and Structure-Based Drug Design to Solve Pharmacokinetic Issues in a Series of Potent 1,2,4-Oxadiazole EthR Inhibitors.
29. NMR structure of the ACID (ACtivator Interacting Domain) of the human mediator Med25 protein
30. Crystal structure of the R450A mutant of the membrane protein FhaC
31. Crystal Structure of Bordetella pertussis BvgS VFT2 domain (Double Mutant F375E/Q461E)
32. Crystal Structure of Bordetella pertussis BvgS periplasmic VFT2 domain
33. EthR from Mycobacterium tuberculosis in complex with compound BDM14950
34. EthR from Mycobacterium tuberculosis in complex with compound BDM14500
35. Structure of the FhaC translocation pore: insights into transport across the bacterial membrane
36. Crystal Structure of GH family 19 chitinase from Carica papaya
37. Structure of the membrane protein fhac: a member of the omp85/tpsb transporter family
38. Structure of a periplasmic transporter
39. crystal structure of papaya glutaminyl cyclase
40. CRYSTAL STRUCTURE OF E.COLI ISOPENTENYL DIPHOSPHATE:DIMETHYLALLYL DIPHOSPHATE ISOMERASE
41. CRYSTAL STRUCTURE OF A D-AMINOPEPTIDASE FROM OCHROBACTRUM ANTHROPI
42. Structural analysis of the allosteric transition ofPseudomonas putidacatabolic ornithine carbamoyltransferase
43. Allosteric regulation in Pseudomonas aeruginosa catabolic ornithine carbamoyltransferase revisited: association of concerted homotropic cooperative interactions and local heterotropic effects
44. ORNITHINE CARBAMOYLTRANSFERASE FROM PYROCOCCUS FURIOSUS
45. ORNITHINE TRANSCARBAMOYLASE FROM PSEUDOMONAS AERUGINOSA
46. FRUCTOSE-1,6-BISPHOSPHATASE (D-FRUCTOSE-1,6-BISPHOSPHATE 1-PHOSPHOHYDROLASE) COMPLEXED WITH THALLIUM IONS (10 MM)
47. Crystal structure of Pseudomonas aeruginosa catabolic ornithine transcarbamoylase at 3.0-A resolution: a different oligomeric organization in the transcarbamoylase family.
48. Crystallographic evidence for the action of potassium, thallium, and lithium ions on fructose-1,6-bisphosphatase.
49. STRUCTURAL ASPECTS OF THE ALLOSTERIC INHIBITION OF FRUCTOSE-1,6-BISPHOSPHATASE BY AMP: THE BINDING OF BOTH THE SUBSTRATE ANALOGUE 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE AND CATALYTIC METAL IONS MONITORED BY X-RAY CRYSTALLOGRAPHY
50. Glycine 122 is essential for cooperativity and binding of Mg2+ to porcine fructose-1,6-bisphosphatase.
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