{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T10:58:06Z","timestamp":1791543486018,"version":"4.3.4"},"reference-count":77,"publisher":"eLife Sciences Publications, Ltd","license":[{"start":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T00:00:00Z","timestamp":1791504000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T00:00:00Z","timestamp":1791504000000},"content-version":"am","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T00:00:00Z","timestamp":1791504000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"National Institutes of Health","award":["F32AI161793"],"award-info":[{"award-number":["F32AI161793"]}]},{"award":["F32AI161793"],"award-info":[{"award-number":["F32AI161793"]}],"id":[{"id":"https:\/\/ror.org\/01cwqze88","id-type":"ROR","asserted-by":"publisher"}]},{"name":"National Science Foundation Graduate Research Fellowship Program","award":["DGE1745303"],"award-info":[{"award-number":["DGE1745303"]}]},{"award":["DGE1745303"],"award-info":[{"award-number":["DGE1745303"]}],"id":[{"id":"https:\/\/ror.org\/021nxhr62","id-type":"ROR","asserted-by":"publisher"}]}],"content-domain":{"domain":["elifesciences.org"],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p>\n                    In\n                    <jats:italic>Mycobacterium tuberculosis<\/jats:italic>\n                    , a prevalent and deadly pathogen, resistance to antibiotics evolves primarily through non-synonymous mutations in proteins. Sequence-based analyses can uncover the genetic basis of antibiotic resistance, but these methods focus on primary sequence and often neglect other biological signals, such as protein structural information. We hypothesize that integrating the structural context of mutations improves the prediction of effects on function and phenotype. We curate high-confidence structural annotations for the\n                    <jats:italic>M. tuberculosis<\/jats:italic>\n                    proteome from 1350 crystallography and 2337 AlphaFold predictions, and mutations from over 31,000\n                    <jats:italic>M. tuberculosis<\/jats:italic>\n                    isolates. We demonstrate that mutations in proteins known to cause resistance are clustered in 3D space, even in proteins where inactivating mutations at any position are thought to cause resistance. We find over 450 proteins in the\n                    <jats:italic>M. tuberculosis<\/jats:italic>\n                    proteome that display signals of clustered mutations, many of which have a known relationship with antibiotic resistance. We show that a supervised classifier trained on 3D distance to known resistance sites alone has an\n                    <jats:italic>F<\/jats:italic>\n                    1 score of 96.5% at classifying mutations as resistance-conferring on a held-out test set. This work demonstrates that protein structure provides useful information for categorizing which variants may cause antibiotic resistance, even when the majority of structures are AI-predicted.\n                  <\/jats:p>","DOI":"10.7554\/elife.109450","type":"journal-article","created":{"date-parts":[[2025,12,12]],"date-time":"2025-12-12T14:30:40Z","timestamp":1765549840000},"update-policy":"https:\/\/doi.org\/10.7554\/elife.109450","source":"Crossref","is-referenced-by-count":0,"title":["The structural context of mutations in proteins predicts their effect on antibiotic resistance"],"prefix":"10.7554","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7548-3682","authenticated-orcid":true,"given":"Anna G","family":"Green","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03vek6s52","id-type":"ROR","asserted-by":"publisher"}],"name":"Department of Biomedical Informatics, Harvard Medical School","place":["Boston, United 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