Sequence of UBA1_HUMAN

E1 ubiquitin-activating enzyme

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Stephen A.G.,Trausch-Azar J.S.,Handley-Gearhart P.M.,Ciechanover A.,Schwartz A.L.

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Gauci S.,Helbig A.O.,Slijper M.,Krijgsveld J.,Heck A.J.,Mohammed S.

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Mayya V.,Lundgren D.H.,Hwang S.-I.,Rezaul K.,Wu L.,Eng J.K.,Rodionov V.,Han D.K.

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Sci. Signal.

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Choudhary C.,Kumar C.,Gnad F.,Nielsen M.L.,Rehman M.,Walther T.C.,Olsen J.V.,Mann M.

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Olsen J.V.,Vermeulen M.,Santamaria A.,Kumar C.,Miller M.L.,Jensen L.J.,Gnad F.,Cox J.,Jensen T.S.,Nigg E.A.,Brunak S.,Mann M.

Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.

Sci. Signal.

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461835

Burkard T.R.,Planyavsky M.,Kaupe I.,Breitwieser F.P.,Buerckstuemmer T.,Bennett K.L.,Superti-Furga G.,Colinge J.

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Rigbolt K.T.,Prokhorova T.A.,Akimov V.,Henningsen J.,Johansen P.T.,Kratchmarova I.,Kassem M.,Mann M.,Olsen J.V.,Blagoev B.

System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.

Sci. Signal.

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Moudry P.,Lukas C.,Macurek L.,Hanzlikova H.,Hodny Z.,Lukas J.,Bartek J.

Ubiquitin-activating enzyme UBA1 is required for cellular response to DNA damage.

Cell Cycle

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N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.

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Zhou H.,Di Palma S.,Preisinger C.,Peng M.,Polat A.N.,Heck A.J.,Mohammed S.

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Bian Y.,Song C.,Cheng K.,Dong M.,Wang F.,Huang J.,Sun D.,Wang L.,Ye M.,Zou H.

An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

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N-terminome analysis of the human mitochondrial proteome.

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Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease.

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Xie S.T.

Expression, purification, and crystal structure of N-terminal domains of human ubiquitin-activating enzyme (E1).

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461844

Ramser J.,Ahearn M.E.,Lenski C.,Yariz K.O.,Hellebrand H.,von Rhein M.,Clark R.D.,Schmutzler R.K.,Lichtner P.,Hoffman E.P.,Meindl A.,Baumbach-Reardon L.

Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy.

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Dlamini N.,Josifova D.J.,Paine S.M.,Wraige E.,Pitt M.,Murphy A.J.,King A.,Buk S.,Smith F.,Abbs S.,Sewry C.,Jacques T.S.,Jungbluth H.

Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene.

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