about
Baulamycins A and B, broad-spectrum antibiotics identified as inhibitors of siderophore biosynthesis in Staphylococcus aureus and Bacillus anthracis.Structural basis of substrate specificity and regiochemistry in the MycF/TylF family of sugar O-methyltransferases.Evolution of Efficient Modular Polyketide Synthases by Homologous RecombinationDiscovery of cahuitamycins as biofilm inhibitors derived from a convergent biosynthetic pathwayBiochemical studies of the lagunamides, potent cytotoxic cyclic depsipeptides from the marine cyanobacterium Lyngbya majuscula.Structural Basis for Cyclopropanation by a Unique Enoyl-Acyl Carrier Protein ReductaseThioesterase domain swapping of a linear polyketide tautomycetin with a macrocyclic polyketide pikromycin in Streptomyces sp. CK4412.Lagunamides A and B: cytotoxic and antimalarial cyclodepsipeptides from the marine cyanobacterium Lyngbya majuscula.Borrelidin Induces the Unfolded Protein Response in Oral Cancer Cells and Chop-Dependent Apoptosis.Aspernolides A and B, butenolides from a marine-derived fungus Aspergillus terreus.Function and Structure of MalA/MalA', Iterative Halogenases for Late-Stage C-H Functionalization of Indole Alkaloids.Discovery of nicoyamycin A, an inhibitor of uropathogenic Escherichia coli growth in low iron environments.Hantupeptin A, a cytotoxic cyclic depsipeptide from a Singapore collection of Lyngbya majuscula.Correction to “Baulamycins A and B, Broad-Spectrum Antibiotics Identified as Inhibitors of Siderophore Biosynthesis in Staphylococcus aureus and Bacillus anthracis”.Chemoenzymatic Dissection of Polyketide β-Branching in the Bryostatin PathwayA Defined and Flexible Pocket Explains Aryl Substrate Promiscuity of the Cahuitamycin Starter Unit-Activating Enzyme CahJDDAP: docking domain affinity and biosynthetic pathway prediction tool for type I polyketide synthases
P50
Q33641697-22946876-38DB-4580-B025-B9AD4C2F6CC0Q35612402-5D6C030A-7013-4046-9DC0-F59EC17CC25EQ35730099-69C29C8A-34A3-40D8-A39B-6F6D3B9B6F23Q35924624-C3D696E8-5755-4648-B3D8-601758B8F0C0Q36096741-5278F78E-912A-4967-8186-22830218E8ECQ36348813-0CB412DC-C356-4E95-BFFB-EFB5A7B23AA2Q37080940-7FFA5D46-54C0-4854-AD01-10058FBA553EQ41934762-5F30C426-34A7-4220-84EC-DE5B771D5722Q42138303-808FA7EF-29F8-49A6-8A86-65A8B7E7FDC6Q46199120-3882A79D-35EB-4BD1-B1E2-0CF635CDF895Q46408284-0647E628-1283-474C-A1BE-FCA1447757A2Q50006927-B9FF8F50-A5EA-4576-AC3E-3D77464335B9Q51672610-A21BAEEA-4A88-439E-AAFE-F5C319DF947EQ55362836-B8CE5F3E-F164-43DB-A526-BC923A07E782Q57255660-25F448FA-EA4B-41E5-AC0B-5225A96A5D65Q88615328-F40185FA-1E6B-44E8-B976-E3147FFA3903Q90025245-A518EED7-6ACD-4C45-8725-AC4A83DFA409
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Ashootosh Tripathi
@ast
Ashootosh Tripathi
@en
Ashootosh Tripathi
@es
Ashootosh Tripathi
@nl
Ashootosh Tripathi
@sl
আশুতোষ ত্রিপাঠী
@bn
type
label
Ashootosh Tripathi
@ast
Ashootosh Tripathi
@en
Ashootosh Tripathi
@es
Ashootosh Tripathi
@nl
Ashootosh Tripathi
@sl
আশুতোষ ত্রিপাঠী
@bn
prefLabel
Ashootosh Tripathi
@ast
Ashootosh Tripathi
@en
Ashootosh Tripathi
@es
Ashootosh Tripathi
@nl
Ashootosh Tripathi
@sl
আশুতোষ ত্রিপাঠী
@bn
P106
P1153
25824084300
P31
P496
0000-0003-2297-8088