A Second, Druggable Binding Site in UDP-Galactopyranose Mutase from Mycobacterium tuberculosis?

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Solution NMR Studies of Mycobacterium tuberculosis Proteins for Antibiotic Target Discovery.Natural and Synthetic Flavonoids as Potent Mycobacterium tuberculosis UGM Inhibitors.Conformational Control of UDP-Galactopyranose Mutase Inhibition.

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A Second, Druggable Binding Site in UDP-Galactopyranose Mutase from Mycobacterium tuberculosis?

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2016 nî lūn-bûn

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A Second, Druggable Binding Si ...... om Mycobacterium tuberculosis?

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A Second, Druggable Binding Si ...... om Mycobacterium tuberculosis?

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A Second, Druggable Binding Si ...... om Mycobacterium tuberculosis?

@en

A Second, Druggable Binding Si ...... om Mycobacterium tuberculosis?

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A Second, Druggable Binding Si ...... om Mycobacterium tuberculosis?

@en

A Second, Druggable Binding Si ...... om Mycobacterium tuberculosis?

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P1476

A Second, Druggable Binding Si ...... om Mycobacterium tuberculosis?

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B Mario Pinto

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David A R Sanders

http://www.w3.org/2001/XMLSchema#string

Jijin R A Kuttiyatveetil

http://www.w3.org/2001/XMLSchema#string

Karin E van Straaten

http://www.w3.org/2001/XMLSchema#string

Nataliya Zalatar

http://www.w3.org/2001/XMLSchema#string

Sankar Mohan

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P2860

The Envelope of Mycobacteria

Comparison of simple potential functions for simulating liquid water

Ligand Binding and Substrate Discrimination by UDP-Galactopyranose Mutase

X-ray crystallography reveals a reduced substrate complex of UDP-galactopyranose mutase poised for covalent catalysis by flavin

Virtual Screening for UDP-Galactopyranose Mutase Ligands Identifies a New Class of Antimycobacterial Agents

Structural basis of substrate binding to UDP-galactopyranose mutase: crystal structures in the reduced and oxidized state complexed with UDP-galactopyranose and UDP

Chemoenzymatic synthesis, inhibition studies, and X-ray crystallographic analysis of the phosphono analog of UDP-Galp as an inhibitor and mechanistic probe for UDP-galactopyranose mutase

Specificity of a UDP-GalNAc pyranose-furanose mutase: a potential therapeutic target for Campylobacter jejuni infections

Structural basis of ligand binding to UDP-galactopyranose mutase from Mycobacterium tuberculosis using substrate and tetrafluorinated substrate analogues

The Amber biomolecular simulation programs

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2264-2273

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scholarly article

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10.1002/CBIC.201600469

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http://www.w3.org/2001/XMLSchema#string

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Cinzia Colombo

Yun Shi

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2016-11-07T00:00:00Z

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27653508

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P921

Mycobacterium tuberculosis

A Second, Druggable Binding Site in UDP-Galactopyranose Mutase from Mycobacterium tuberculosis?

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P2860

P2860

A Second, Druggable Binding Site in UDP-Galactopyranose Mutase from Mycobacterium tuberculosis?

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P1476

P2093

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P31

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P433

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P50

P577

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P921