相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Role of non-active site residues in maintaining New Delhi metallo-β-lactamase-1(NDM-1) function: an approach of site-directed mutagenesis and docking
Abid Ali et al.
FEMS MICROBIOLOGY LETTERS (2021)
Drug repurposing against arabinosyl transferase (EmbC) of Mycobacterium tuberculosis: Essential dynamics and free energy minima based binding mechanics analysis
Aditi Singh et al.
GENE (2019)
Pyrazinamide drug resistance in RpsA mutant ( increment 438A) of Mycobacterium tuberculosis: Dynamics of essential motions and free-energy landscape analysis
Aditi Singh et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2019)
PubChem 2019 update: improved access to chemical data
Sunghwan Kim et al.
NUCLEIC ACIDS RESEARCH (2019)
Designing of inhibitors against CTX-M-15 type beta-lactamase: potential drug candidate against -lactamases-producing multi-drug-resistant bacteria
Abid Ali et al.
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2018)
Simulation Based Investigation of Deleterious nsSNPs in ATXN2 Gene and Its Structural Consequence Toward Spinocerebellar Ataxia
Siddharth Sinha et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2018)
Active-Site Conformational Fluctuations Promote the Enzymatic Activity of NDM-1
Hongmin Zhang et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2018)
Metallo-β-lactamase inhibitors by bioisosteric replacement: Preparation, activity and binding
Susann Skagseth et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2017)
Mechanistic Principles Behind Molecular Mechanism of Rifampicin Resistance in Mutant RNA Polymerase Beta Subunit of Mycobacterium tuberculosis
Aditi Singh et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2017)
Potential inhibitors designed against NDM-1 type metallo-β-actamases: an attempt to enhance efficacies of antibiotics against multi-drug-resistant bacteria
Asad U. Khan et al.
SCIENTIFIC REPORTS (2017)
Fragment based G-QSAR and molecular dynamics based mechanistic simulations into hydroxamic-based HDAC inhibitors against spinocerebellar ataxia
Siddharth Sinha et al.
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2016)
4,5-Disubstituted 6-Aryloxy-1,3-dihydrobenzo[c][1,2]oxaboroles Are Broad-Spectrum Serine β-Lactarnase Inhibitors
David C. McKinney et al.
ACS INFECTIOUS DISEASES (2015)
Understanding the fate of an anesthetic, nalorphine upon interaction with human serum albumin: a photophysical and mass-spectroscopy approach
Zhengyan Chen et al.
RSC ADVANCES (2014)
Structural Insight into Potent Broad-Spectrum Inhibition with Reversible Recyclization Mechanism: Avibactam in Complex with CTX-M-15 and Pseudomonas aeruginosa AmpC β-Lactamases
Sushmita D. Lahiri et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2013)
Study on the interaction of the epilepsy drug, zonisamide with human serum albumin (HSA) by spectroscopic and molecular docking techniques
Nahid Shahabadi et al.
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY (2013)
Crystal structure of NDM-1 reveals a common β-lactam hydrolysis mechanism
HongMin Zhang et al.
FASEB JOURNAL (2011)
Structure of Apo- and Monometalated Forms of NDM-1-A Highly Potent Carbapenem-Hydrolyzing Metallo-β-Lactamase
Youngchang Kim et al.
PLOS ONE (2011)
Updated Functional Classification of beta-Lactamases
Karen Bush et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2010)
Mechanistic Studies of the Inactivation of TEM-1 and P99 by NXL104, a Novel Non-β-Lactam β-Lactamase Inhibitor
Therese Stachyra et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2010)
Three Decades of beta-Lactamase Inhibitors
Sarah M. Drawz et al.
CLINICAL MICROBIOLOGY REVIEWS (2010)
Software News and Update AutoDock Vina: Improving the Speed and Accuracy of Docking with a New Scoring Function, Efficient Optimization, and Multithreading
Oleg Trott et al.
JOURNAL OF COMPUTATIONAL CHEMISTRY (2010)
Genetic and structural insights into the dissemination potential of the extremely broad-spectrum class A β-lactamase KPC-2 identified in an Escherichia coli strain and an Enterobacter cloacae strain isolated from the same patient in France
Stephanie Petrella et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2008)
PRODRG:: a tool for high-throughput crystallography of protein-ligand complexes
AW Schüttelkopf et al.
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY (2004)
Determination of minimum inhibitory concentrations
JM Andrews
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY (2001)