{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T16:12:59Z","timestamp":1790266379733,"version":"4.1.0"},"reference-count":0,"publisher":"Oxford University Press (OUP)","license":[{"start":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T00:00:00Z","timestamp":1790208000000},"content-version":"am","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Glycoside hydrolases (GHs) accelerate glycosidic bond cleavage by coupling active-site architecture, the geometry required for substitution at the anomeric center, and the conformational landscape of the \u22121 sugar. This coupling is often summarized as family-dependent conformational itineraries that connect Michaelis complexes to oxocarbenium-ion-like transition states (and, for retaining enzymes, to covalent intermediates). However, crystallographic snapshots sometimes reveal complexes in which the \u22121 sugar remains close to a ground-state-like 4C\u2081 chair or adopts noncanonical puckers such as E\u2085. In this Review, we reassess such observations within a cautious physical-organic framework. Here, \u201cexception\u201d is used in a mechanistic rather than statistical sense: the aim is to document and interpret departures from the conformational behaviour expected from accepted stereochemistry itinerary relationships, not to estimate the relative abundance of such cases in the Protein Data Bank. Chair-like 4C\u2081 complexes should not be interpreted as evidence for a new transition-state geometry; rather, they may represent recognition or pre-reactive minima in which catalytic residues are positioned near C1 but additional late, transient, or ensemble distortion is still required to reach an in-line, oxocarbenium-ion-like transition state. We further discuss how metal coordination and active-site constraints in \u03b1-mannosidases can stabilize alternative pre-reactive basins\u2014exemplified by E\u2085 complexes in GH38 and GH92\u2014while preserving access to transition-state-competent regions. Finally, we outline how structural descriptors, on-enzyme dynamics, and intrinsic quantum-mechanical \u201cpreactivation\u201d indices can help distinguish genuinely productive noncanonical states from crystallographic ground-state snapshots.<\/jats:p>","DOI":"10.1093\/glycob\/cwag082","type":"journal-article","created":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T11:57:34Z","timestamp":1790164654000},"source":"Crossref","is-referenced-by-count":0,"title":["Conformational exceptions in glycoside hydrolase reactivity"],"prefix":"10.1093","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7596-8161","authenticated-orcid":false,"given":"Santiago","family":"Alonso-Gil","sequence":"first","affiliation":[{"name":"Institut Laue-Langevin , Grenoble ,","place":["France"]},{"name":"Laboratory of Computer-Aided Molecular Design, Division of Medicinal Chemistry, Otto-Loewi Research Center, Medical University of Graz , Neue Stiftintalstr. 6\/III, A-8010 Graz ,","place":["Austria"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2026,9,24]]},"container-title":["Glycobiology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/academic.oup.com\/glycob\/advance-article-pdf\/doi\/10.1093\/glycob\/cwag082\/71382110\/cwag082.pdf","content-type":"application\/pdf","content-version":"am","intended-application":"syndication"},{"URL":"https:\/\/academic.oup.com\/glycob\/advance-article-pdf\/doi\/10.1093\/glycob\/cwag082\/71382110\/cwag082.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T15:45:31Z","timestamp":1790264731000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/glycob\/advance-article\/doi\/10.1093\/glycob\/cwag082\/8833813"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,9,24]]},"references-count":0,"URL":"https:\/\/doi.org\/10.1093\/glycob\/cwag082","relation":{},"ISSN":["1460-2423"],"issn-type":[{"value":"1460-2423","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,9,24]]},"article-number":"cwag082"}}