{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T18:59:14Z","timestamp":1790189954007,"version":"4.1.0"},"reference-count":49,"publisher":"American Association for the Advancement of Science (AAAS)","issue":"39","funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["AI151638"],"award-info":[{"award-number":["AI151638"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R35GM151043"],"award-info":[{"award-number":["R35GM151043"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["www.science.org"],"crossmark-restriction":true},"short-container-title":["Sci. Adv."],"published-print":{"date-parts":[[2026,9,25]]},"abstract":"<jats:p>\n                    SAMD9 and SAMD9L (SAMD9\/9L) are large cytosolic proteins essential for hematopoietic homeostasis and antiviral defense (\n                    <jats:xref ref-type=\"bibr\">\n                      <jats:italic toggle=\"yes\">1<\/jats:italic>\n                    <\/jats:xref>\n                    \u2013\n                    <jats:xref ref-type=\"bibr\">\n                      <jats:italic toggle=\"yes\">3<\/jats:italic>\n                    <\/jats:xref>\n                    ). Germline gain-of-function (GoF) mutations in SAMD9\/9L cause severe multisystem disorders and predispose to leukemia, but the mechanisms that regulate SAMD9\/9L activity and how pathogenic mutations disrupt these processes remain poorly understood. Here, we report cryo\u2013electron microscopy structures of human SAMD9 in multiple conformational and oligomeric states. SAMD9 predominantly adopts a closed, autoinhibited conformation stabilized by a central ATP-bound nucleotide-binding oligomerization domain (NOD) and an extensive network of intramolecular interactions. Recurrent patient-derived GoF mutations localize to and destabilize these intramolecular interfaces, whereas structure-guided compensatory mutations that restabilize these interfaces restore autoinhibition. We further identify low-abundance asymmetric SAMD9 dimers in which one protomer undergoes large conformational changes and establishes intermolecular interactions that are essential for SAMD9 activation. Together, these findings define the structural basis of SAMD9 autoinhibition and reveal how human GoF mutations disrupt this regulatory mechanism to drive disease.\n                  <\/jats:p>","DOI":"10.1126\/sciadv.aeg3967","type":"journal-article","created":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T17:59:49Z","timestamp":1790186389000},"update-policy":"https:\/\/doi.org\/10.34133\/aaas_crossmark","source":"Crossref","is-referenced-by-count":0,"title":["Structural mechanisms of SAMD9 autoinhibition and pathogenic dysregulation"],"prefix":"10.1126","volume":"12","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1908-617X","authenticated-orcid":true,"given":"Zongjun","family":"Mou","sequence":"first","affiliation":[{"name":"Department of Physiology and Biophysics, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0696-8907","authenticated-orcid":true,"given":"Fushun","family":"Zhang","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Immunology and Molecular Genetics, Joe R. &amp; Teresa Lozano Long School of Medicine, The University of Texas at San Antonio, San Antonio, TX 78229, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5206-2738","authenticated-orcid":true,"given":"Marisol","family":"Morales","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Immunology and Molecular Genetics, Joe R. &amp; Teresa Lozano Long School of Medicine, The University of Texas at San Antonio, San Antonio, TX 78229, 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