| Literature DB >> 21988105 |
Zoë Fisher1, Andrey Y Kovalevsky, Marat Mustyakimov, David N Silverman, Robert McKenna, Paul Langan.
Abstract
The neutron structure of wild-type human carbonic anhydrase II at pH 7.8 has been determined to 2.0 Å resolution. Detailed analysis and comparison to the previously determined structure at pH 10.0 show important differences in the protonation of key catalytic residues in the active site as well as a rearrangement of the H-bonded water network. For the first time, a completed H-bonded network stretching from the Zn-bound solvent to the proton shuttling residue, His64, has been directly observed.Entities:
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Year: 2011 PMID: 21988105 PMCID: PMC3371383 DOI: 10.1021/bi201487b
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162