Chemical Mimics of Aspartate-Directed Proteases: Predictive and Strictly Specific Hydrolysis of a Globular Protein at Asp-X Sequence Promoted by Polyoxometalate Complexes Rationalized by a Combined Experimental and Theoretical Approach.
Amino Acid Sequence
Aspartic Acid
/ chemistry
Binding Sites
Biomimetic Materials
/ chemistry
Catalysis
Coordination Complexes
/ chemistry
Hemoglobins
/ chemistry
Hydrolysis
Magnetic Resonance Spectroscopy
Molecular Conformation
Molecular Docking Simulation
Peptide Hydrolases
/ chemistry
Thermodynamics
Tungsten Compounds
/ chemistry
Zirconium
/ chemistry
catalysis
hemoglobin
hydrolysis
metaloproteases
polyoxometalates
Journal
Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783
Informations de publication
Date de publication:
13 Nov 2019
13 Nov 2019
Historique:
received:
11
06
2019
revised:
13
08
2019
pubmed:
31
8
2019
medline:
21
11
2019
entrez:
31
8
2019
Statut:
ppublish
Résumé
Creating efficient and residue-directed artificial proteases is a challenging task due to the extreme inertness of the peptide bond, combined with the difficulty of achieving specific interactions between the catalysts and the protein side chains. Herein we report strictly site-selective hydrolysis of a multi-subunit globular protein, hemoglobin (Hb) from bovine blood, by a range of Zr
Identifiants
pubmed: 31469197
doi: 10.1002/chem.201902675
doi:
Substances chimiques
Coordination Complexes
0
Hemoglobins
0
Tungsten Compounds
0
polyoxometalate I
0
Aspartic Acid
30KYC7MIAI
Zirconium
C6V6S92N3C
Peptide Hydrolases
EC 3.4.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
14370-14381Subventions
Organisme : KU Leuven
ID : OT/13/060
Informations de copyright
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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