Sequence information
Variant position: 207 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 729 The length of the canonical sequence.
Location on the sequence:
RAVLRKDHQKKYGATVDLWS
I GVTFYHAATGSLPFRPFEGP
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human RAVLRKDHQKKYGATVDLWSI GVTFYHAATGSLPFRPFEGP
Mouse RAVLRKDHQKKYGATVDLWSV GVTFYHAATGSLPFRPFEGP
Xenopus laevis RAVLRKEHQKKYSATVDLWSI GVTFYHAATGSLPFRPFEGP
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
Chain
1 – 729
Serine/threonine-protein kinase TBK1
Domain
9 – 310
Protein kinase
Helix
202 – 216
Literature citations
Mutations in the TLR3 signaling pathway and beyond in adult patients with herpes simplex encephalitis.
Moerk N.; Kofod-Olsen E.; Soerensen K.B.; Bach E.; Oerntoft T.F.; Oestergaard L.; Paludan S.R.; Christiansen M.; Mogensen T.H.;
Genes Immun. 16:552-566(2015)
Cited for: INVOLVEMENT IN IIAE8; VARIANT IIAE8 VAL-207;
Disclaimer:
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.