α-Glucan biosynthesis and the GlgE pathway in Mycobacterium tuberculosis

S Bornemann - Biochemical society transactions, 2016 - portlandpress.com
It has long been reported that Mycobacterium tuberculosis is capable of synthesizing the α-
glucan glycogen. However, what makes this bacterium stand out is that it coats itself in a …

In silico discovery and in vitro activity of inhibitors against Mycobacterium tuberculosis 7,8-diaminopelargonic acid synthase (Mtb BioA)

JB Billones, MCO Carrillo, VG Organo… - Drug design …, 2017 - Taylor & Francis
Computer-aided drug discovery and development approaches such as virtual screening,
molecular docking, and in silico drug property calculations have been utilized in this effort to …

Structure-based in silico and in vitro analysis reveals asiatic acid as novel potential inhibitor of Mycobacterium tuberculosis maltosyl transferase

K Singh, A Sharma, TK Upadhyay… - … -Aided Drug Design, 2022 - ingentaconnect.com
Aims: The present study aimed to search for novel potent inhibitor (s) against the recently
discovered maltosyltransferase (GlgE) target of M. tb. Background: GlgE belongs to an α …

In ovo and in silico evaluation of the anti-angiogenic potential of syringin

CA Aventurado, JB Billones, RD Vasquez… - Drug Design …, 2020 - Taylor & Francis
Introduction Cancer is considered as one of the deadliest human diseases today.
Angiogenesis, the propagation of new blood vessels from pre-existing vasculature, is a …

[PDF][PDF] Structure-based discovery of inhibitors against MurE in methicillin-resistant Staphylococcus aureus

JB Billones, MAT Bangalan - Oriental Journal of Chemistry, 2019 - academia.edu
The rise of superbugs is a serious public health concern. It is estimated to kill around 10
million people a year by 2050 and will overtake cancer as the number one cause of death …

Ligand-bound structures and site-directed mutagenesis identify the acceptor and secondary binding sites of Streptomyces coelicolor maltosyltransferase GlgE

K Syson, CEM Stevenson, F Miah, JE Barclay… - Journal of Biological …, 2016 - ASBMB
GlgE is a maltosyltransferase involved in α-glucan biosynthesis in bacteria that has been
genetically validated as a target for tuberculosis therapies. Crystals of the Mycobacterium …

In silico discovery of natural products against dengue rna-dependent rna polymerase drug target

JB Billones, NAB Clavio - Chem-Bio Informatics Journal, 2021 - jstage.jst.go.jp
The viral infection caused by the dengue virus (DENV) is one of the most challenging
diseases in the tropical regions of the world. The absence of drugs for dengue to this date …

[PDF][PDF] Retusenol Potentially Inhibits Putative Drug Targets for Tuberculosis, Cardiovascular Diseases, Cancer and HIV: A Reverse Docking Study

PD Rariza, JB Billones - Oriental Journal of Chemistry, 2018 - researchgate.net
Retusenol is a new triterpene discovered from the leaf extracts of Atalantia retusa Merr., a
Philippine endemic shrub. With the emergence of drug resistance and drug tolerance in …

Glycoconjugate-Based Inhibitors of Mycobacterium Tuberculosis GlgE

SK Veleti, SJ Sucheck - Coupling and Decoupling of Diverse Molecular …, 2018 - Springer
Tuberculosis (TB) is the leading cause of death globally as a result of a single infectious
disease. A staggering 6 million new cases were reported in the 2014. In order to eradicate …

[PDF][PDF] Karl Syson, Clare EM Stevenson, Farzana Miah, J. Elaine Barclay, Minhong Tang, Andrii

AMR Gorelik, DM Lawson, S Bornemann - 2016 - researchgate.net
GlgE is a maltosyltransferase involved in αglucan biosynthesis in bacteria that has been
genetically validated as a target for tuberculosis therapies. Crystals of the Mycobacterium …