Artur Mucha - Concepedia

Author

Artur Mucha

Wrocław University of Science and Technology ORCID

Also Known As

A. MUCHA, A. Mucha, Abel Moises Castro Mucha, Arthur Mucha, Artur Mucha, Mucha, A., Mucha, Artur

101

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Wrocław University of Science and Technology University of Opole University of Wrocław National and Kapodistrian University of Athens AGH University of Krakow

About

Artur Mucha is an author at Wrocław University of Science and Technology specializing in biochemistry, natural sciences, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	21	32	1.8K
2	Natural Sciences	18	25	1.7K
3	Medicine	17	22	1.6K
4	Engineering	8	8	300
5	Biomolecular Engineering	7	7	272

Artur Mucha

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Remarkable Potential of the α-Aminophosphonate/Phosphinate Structural Motif in Medicinal Chemistry Artur Mucha, Paweł Kafarski, Łukasz Berlicki Journal of Medicinal Chemistry Molecular RecognitionMedicinal ChemistryRemarkable PotentialBioorganic ChemistryBiochemistry	2011	643
The Most Potent Organophosphorus Inhibitors of Leucine Aminopeptidase. Structure-Based Design, Chemistry, and Activity Jolanta Grembecka, Artur Mucha, Tomasz Cierpicki, Journal of Medicinal Chemistry	2003	219
Structural basis for the inhibition of the essential <i>Plasmodium falciparum</i> M1 neutral aminopeptidase Sheena McGowan, Corrine J. Porter, Jonathan Lowther, Proceedings of the National Academy of Sciences Protein FunctionAmino AcidsBiochemistryProtein AssemblyProtease Active Site	2009	152
Characterization of the Plasmodium falciparum M17 Leucyl Aminopeptidase Colin M. Stack, Jonathan Lowther, Eithne Cunningham, Journal of Biological Chemistry Protein ChemistryAmino AcidsBiochemistryAntiparasitic AgentNatural Sciences	2006	121
Crystal Structures of Active LytM Małgorzata Firczuk, Artur Mucha, Matthias Bochtler Journal of Molecular Biology Materials ScienceCrystal StructureEngineeringCrystal MaterialChemistry	2005	112
Phosphinic Pseudo-Tripeptides as Potent Inhibitors of Matrix Metalloproteinases: A Structure−Activity Study Stamatia Vassiliou, Artur Mucha, Philippe Cuniasse, Journal of Medicinal Chemistry Protein ChemistryInhibitory ActivityMedicinal ChemistryBiochemistryNatural Sciences	1999	111
Identification of Phosphinate Dipeptide Analog Inhibitors Directed against the <i>Plasmodium </i><i>falciparum</i> M17 Leucine Aminopeptidase as Lead Antimalarial Compounds Tina S. Skinner‐Adams, Jonathan Lowther, Franka Teuscher, Journal of Medicinal Chemistry	2007	99
Structure of the <i>Plasmodium falciparum</i> M17 aminopeptidase and significance for the design of drugs targeting the neutral exopeptidases Sheena McGowan, Christine A. Oellig, Woldeamanuel A. Birru, Proceedings of the National Academy of Sciences Protein AssemblyBiomolecular Structure PredictionAntiparasitic AgentMalariaActive Sites	2010	98
Structural Insights into Substrate Selectivity and Activity of Bacterial Polyphosphate Kinases B. Nocek, Anna N. Khusnutdinova, M. Ruszkowski, ACS Catalysis Substrate SelectivityBiochemistryBiomolecular Structure PredictionNatural SciencesPolyp Kinases	2018	82
Membrane Type-1 Matrix Metalloprotease and Stromelysin-3 Cleave More Efficiently Synthetic Substrates Containing Unusual Amino Acids in Their P1′ Positions Artur Mucha, Philippe Cuniasse, Rama Kannan, Journal of Biological Chemistry	1998	61

Page 1