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Origins of stereoselectivity in evolved ketoreductases

Origins of stereoselectivity in evolved ketoreductases

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_jstor_primary_26466210

Origins of stereoselectivity in evolved ketoreductases

About this item

Full title

Origins of stereoselectivity in evolved ketoreductases

Publisher

United States: National Academy of Sciences

Journal title

Proceedings of the National Academy of Sciences - PNAS, 2015-12, Vol.112 (51), p.E7065-E7072

Language

English

Formats

Publication information

Publisher

United States: National Academy of Sciences

More information

Scope and Contents

Contents

Mutants ofLactobacillus kefirshort-chain alcohol dehydrogenase, used here as ketoreductases (KREDs), enantioselectively reduce the pharmaceutically relevant substrates 3-thiacyclopentanone and 3-oxacyclopentanone. These substrates differ by only the heteroatom (S or O) in the ring, but the KRED mutants reduce them with different enantioselectivitie...

Alternative Titles

Full title

Origins of stereoselectivity in evolved ketoreductases

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_jstor_primary_26466210

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_jstor_primary_26466210

Other Identifiers

ISSN

0027-8424

E-ISSN

1091-6490

DOI

10.1073/pnas.1507910112

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