146 related articles for article (PubMed ID: 28422240)
1. Zwitterionic pyrrolidene-phosphonates: inhibitors of the glycoside hydrolase-like phosphorylase Streptomyces coelicolor GlgEI-V279S.
Veleti SK; Petit C; Lindenberger JJ; Ronning DR; Sucheck SJ
Org Biomol Chem; 2017 May; 15(18):3884-3891. PubMed ID: 28422240
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of 2-deoxy-2,2-difluoro-α-maltosyl fluoride and its X-ray structure in complex with Streptomyces coelicolor GlgEI-V279S.
Thanna S; Lindenberger JJ; Gaitonde VV; Ronning DR; Sucheck SJ
Org Biomol Chem; 2015 Jul; 13(27):7542-50. PubMed ID: 26072729
[TBL] [Abstract][Full Text] [Related]
3. Correction: Zwitterionic pyrrolidene-phosphonates: inhibitors of the glycoside hydrolase-like phosphorylase Streptomyces coelicolor GlgEI-V279S.
Veleti SK; Petit C; Lindenberger JJ; Ronning DR; Sucheck SJ
Org Biomol Chem; 2017 Aug; 15(31):6679. PubMed ID: 28752886
[TBL] [Abstract][Full Text] [Related]
4. Crystal structures of Mycobacterium tuberculosis GlgE and complexes with non-covalent inhibitors.
Lindenberger JJ; Veleti SK; Wilson BN; Sucheck SJ; Ronning DR
Sci Rep; 2015 Aug; 5():12830. PubMed ID: 26245983
[TBL] [Abstract][Full Text] [Related]
5. Synthesis of a poly-hydroxypyrolidine-based inhibitor of Mycobacterium tuberculosis GlgE.
Veleti SK; Lindenberger JJ; Thanna S; Ronning DR; Sucheck SJ
J Org Chem; 2014 Oct; 79(20):9444-50. PubMed ID: 25137149
[TBL] [Abstract][Full Text] [Related]
6. Stereoselective synthesis of a 4-⍺-glucoside of valienamine and its X-ray structure in complex with Streptomyces coelicolor GlgE1-V279S.
Si A; Jayasinghe TD; Thanvi R; Kapil S; Ronning DR; Sucheck SJ
Sci Rep; 2021 Jun; 11(1):13413. PubMed ID: 34183716
[TBL] [Abstract][Full Text] [Related]
7. Synthesis of C
Thanvi R; Jayasinghe TD; Kapil S; Obadawo BS; Ronning DR; Sucheck SJ
Front Chem; 2022; 10():950433. PubMed ID: 36157042
[TBL] [Abstract][Full Text] [Related]
8. Structural insight into how Streptomyces coelicolor maltosyl transferase GlgE binds α-maltose 1-phosphate and forms a maltosyl-enzyme intermediate.
Syson K; Stevenson CE; Rashid AM; Saalbach G; Tang M; Tuukkanen A; Svergun DI; Withers SG; Lawson DM; Bornemann S
Biochemistry; 2014 Apr; 53(15):2494-504. PubMed ID: 24689960
[TBL] [Abstract][Full Text] [Related]
9. Synthesis of a C-phosphonate mimic of maltose-1-phosphate and inhibition studies on Mycobacterium tuberculosis GlgE.
Veleti SK; Lindenberger JJ; Ronning DR; Sucheck SJ
Bioorg Med Chem; 2014 Feb; 22(4):1404-11. PubMed ID: 24461562
[TBL] [Abstract][Full Text] [Related]
10. Ligand-bound Structures and Site-directed Mutagenesis Identify the Acceptor and Secondary Binding Sites of Streptomyces coelicolor Maltosyltransferase GlgE.
Syson K; Stevenson CE; Miah F; Barclay JE; Tang M; Gorelik A; Rashid AM; Lawson DM; Bornemann S
J Biol Chem; 2016 Oct; 291(41):21531-21540. PubMed ID: 27531751
[TBL] [Abstract][Full Text] [Related]
11. Structure of Streptomyces maltosyltransferase GlgE, a homologue of a genetically validated anti-tuberculosis target.
Syson K; Stevenson CEM; Rejzek M; Fairhurst SA; Nair A; Bruton CJ; Field RA; Chater KF; Lawson DM; Bornemann S
J Biol Chem; 2011 Nov; 286(44):38298-38310. PubMed ID: 21914799
[TBL] [Abstract][Full Text] [Related]
12. Correction: Synthesis of 2-deoxy-2,2-difluoro-α-maltosyl fluoride and its X-ray structure in complex with Streptomyces coelicolor GlgEI-V279S.
Thanna S; Lindenberger JJ; Gaitonde VV; Ronning DR; Sucheck SJ
Org Biomol Chem; 2015 Aug; 13(29):8080. PubMed ID: 26134153
[TBL] [Abstract][Full Text] [Related]
13. Structure of a 6-pyruvoyltetrahydropterin synthase homolog from Streptomyces coelicolor.
Spoonamore JE; Roberts SA; Heroux A; Bandarian V
Acta Crystallogr Sect F Struct Biol Cryst Commun; 2008 Oct; 64(Pt 10):875-9. PubMed ID: 18931427
[TBL] [Abstract][Full Text] [Related]
14. Nanomolar competitive inhibitors of Mycobacterium tuberculosis and Streptomyces coelicolor type II dehydroquinase.
Prazeres VF; Sánchez-Sixto C; Castedo L; Lamb H; Hawkins AR; Riboldi-Tunnicliffe A; Coggins JR; Lapthorn AJ; González-Bello C
ChemMedChem; 2007 Feb; 2(2):194-207. PubMed ID: 17245805
[TBL] [Abstract][Full Text] [Related]
15. Rational design of new bifunctional inhibitors of type II dehydroquinase.
Toscano MD; Stewart KA; Coggins JR; Lapthorn AJ; Abell C
Org Biomol Chem; 2005 Sep; 3(17):3102-4. PubMed ID: 16106291
[TBL] [Abstract][Full Text] [Related]
16. Stereoselective synthesis and glycosidase inhibitory activity of 3,4-dihydroxy-pyrrolidin-2-one, 3,4-dihydroxy-piperidin-2-one and 1,2-dihydroxy-pyrrolizidin-3-one.
Coutrot P; Claudel S; Didierjean C; Grison C
Bioorg Med Chem Lett; 2006 Jan; 16(2):417-20. PubMed ID: 16271473
[TBL] [Abstract][Full Text] [Related]
17. Design, synthesis, and structural studies on potent biaryl inhibitors of type II dehydroquinases.
Payne RJ; Riboldi-Tunnicliffe A; Kerbarh O; Abell AD; Lapthorn AJ; Abell C
ChemMedChem; 2007 Jul; 2(7):1010-3. PubMed ID: 17487901
[No Abstract] [Full Text] [Related]
18. Modeling of a new tubercular maltosyl transferase, GlgE, study of its binding sites and virtual screening.
Sengupta S; Roy D; Bandyopadhyay S
Mol Biol Rep; 2014 Jun; 41(6):3549-60. PubMed ID: 24820953
[TBL] [Abstract][Full Text] [Related]
19. Human liver glycogen phosphorylase inhibitors bind at a new allosteric site.
Rath VL; Ammirati M; Danley DE; Ekstrom JL; Gibbs EM; Hynes TR; Mathiowetz AM; McPherson RK; Olson TV; Treadway JL; Hoover DJ
Chem Biol; 2000 Sep; 7(9):677-82. PubMed ID: 10980448
[TBL] [Abstract][Full Text] [Related]
20. NgcE
Iinuma C; Saito A; Ohnuma T; Tenconi E; Rosu A; Colson S; Mizutani Y; Liu F; Świątek-Połatyńska M; van Wezel GP; Rigali S; Fujii T; Miyashita K
Microbes Environ; 2018 Sep; 33(3):272-281. PubMed ID: 30089751
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]