synaptotagmin-1 isoform 1 [Homo sapiens]

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Expanding the genotype and phenotype spectrum of SYT1-associated neurodevelopmental disorder. [Genet Med. 2022]
Expanding the genotype and phenotype spectrum of SYT1-associated neurodevelopmental disorder.
Melland H, Bumbak F, Kolesnik-Taylor A, Ng-Cordell E, John A, Constantinou P, Joss S, Larsen M, Fagerberg C, Laulund LW, et al. Genet Med. 2022 Apr; 24(4):880-893. Epub 2022 Jan 29.
The Synaptotagmin-1 C2B Domain Is a Key Regulator in the Stabilization of the Fusion Pore. [J Chem Theory Comput. 2020]
The Synaptotagmin-1 C2B Domain Is a Key Regulator in the Stabilization of the Fusion Pore.
Caparotta M, Tomes CN, Mayorga LS, Masone D. J Chem Theory Comput. 2020 Dec 8; 16(12):7840-7851. Epub 2020 Nov 9.
Molecular Basis for Synaptotagmin-1-Associated Neurodevelopmental Disorder. [Neuron. 2020]
Molecular Basis for Synaptotagmin-1-Associated Neurodevelopmental Disorder.
Bradberry MM, Courtney NA, Dominguez MJ, Lofquist SM, Knox AT, Sutton RB, Chapman ER. Neuron. 2020 Jul 8; 107(1):52-64.e7. Epub 2020 May 1.