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Please use this identifier to cite or link to this item: http://repository.iitr.ac.in/handle/123456789/1494
Title: Ligand-bound structures of 3-deoxy-d-manno-octulosonate 8-phosphate phosphatase from Moraxella catarrhalis reveal a water channel connecting to the active site for the second step of catalysis
Authors: Dhindwal S.
Priyadarshini P.
Patil D.N.
Tapas S.
Kumar, P.
Tomar, Shailly
Kumar, Pravindra R.Manish
Published in: Acta Crystallographica Section D: Biological Crystallography
Abstract: KdsC, the third enzyme of the 3-deoxy-d-manno-octulosonic acid (KDO) biosynthetic pathway, catalyzes a substrate-specific reaction to hydrolyze 3-deoxy-d-manno-octulosonate 8-phosphate to generate a molecule of KDO and phosphate. KdsC is a phosphatase that belongs to the C0 subfamily of the HAD superfamily. To understand the molecular basis for the substrate specificity of this tetrameric enzyme, the crystal structures of KdsC from Moraxella catarrhalis (Mc-KdsC) with several combinations of ligands, namely metal ion, citrate and products, were determined. Various transition states of the enzyme have been captured in these crystal forms. The ligand-free and ligand-bound crystal forms reveal that the binding of ligands does not cause any specific conformational changes in the active site. However, the electron-density maps clearly showed that the conformation of KDO as a substrate is different from the conformation adopted by KDO when it binds as a cleaved product. Furthermore, structural evidence for the existence of an intersubunit tunnel has been reported for the first time in the C0 subfamily of enzymes. A role for this tunnel in transferring water molecules from the interior of the tetrameric structure to the active-site cleft has been proposed. At the active site, water molecules are required for the formation of a water bridge that participates as a proton shuttle during the second step of the two-step phosphoryl-transfer reaction. In addition, as the KDO biosynthesis pathway is a potential antibacterial target, pharmacophore-based virtual screening was employed to identify inhibitor molecules for the Mc-KdsC enzyme. © 2015.
Citation: Acta Crystallographica Section D: Biological Crystallography(2015), 71(): 239-255
URI: https://doi.org/10.1107/S1399004714025218
http://repository.iitr.ac.in/handle/123456789/1494
Issue Date: 2015
Publisher: International Union of Crystallography
Keywords: 3-deoxy-d-manno-octulosonate 8-phosphate phosphatase
KDO biosynthetic pathway
KdsC
ISSN: 9074449
Author Scopus IDs: 36082537700
36519717800
26431600400
35491918300
57204102455
57203506001
55064809000
Author Affiliations: Dhindwal, S., Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247 667, India
Priyadarshini, P., Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Haridwar, Uttarakhand, 247 667, Indi
Corresponding Author: Kumar, P.; Department of Biotechnology, Indian Institute of Technology RoorkeeIndia
Appears in Collections:Journal Publications [BT]

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