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6HCZ

Sjoegren syndrome/scleroderma autoantigen 1 (SSSCA1)

Summary for 6HCZ
Entry DOI10.2210/pdb6hcz/pdb
DescriptorSjoegren syndrome/scleroderma autoantigen 1, FORMIC ACID, ZINC ION, ... (4 entities in total)
Functional Keywordssssca1, zinc binding, e3 ubiquitin ligase, intrinsically disordered protein (idp), wnt pathway, tankyrase binding, metal binding protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight43169.48
Authors
Morth, J.P.,Perdreau-Dahl, H. (deposition date: 2018-08-17, release date: 2020-03-18, Last modification date: 2024-05-15)
Primary citationPerdreau-Dahl, H.,Progida, C.,Barfeld, S.J.,Guldsten, H.,Thiede, B.,Arntzen, M.,Bakke, O.,Mills, I.G.,Krauss, S.,Morth, J.P.
Sjogren syndrome/scleroderma autoantigen 1 is a direct Tankyrase binding partner in cancer cells.
Commun Biol, 3:123-123, 2020
Cited by
PubMed Abstract: Sjögren syndrome/scleroderma autoantigen 1 (SSSCA1) was first described as an auto-antigen over-expressed in Sjögren's syndrome and in scleroderma patients. SSSCA1 has been linked to mitosis and centromere association and as a potential marker candidate in diverse solid cancers. Here we characterize SSSCA1 for the first time, to our knowledge, at the molecular, structural and subcellular level. We have determined the crystal structure of a zinc finger fold, a zinc ribbon domain type 2 (ZNRD2), at 2.3 Å resolution. We show that the C-terminal domain serves a dual function as it both behaves as the interaction site to Tankyrase 1 (TNKS1) and as a nuclear export signal. We identify TNKS1 as a direct binding partner of SSSCA1, map the binding site to TNKS1 ankyrin repeat cluster 2 (ARC2) and thus define a new binding sequence. We experimentally verify and map a new nuclear export signal sequence in SSSCA1.
PubMed: 32170109
DOI: 10.1038/s42003-020-0851-2
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

237992

数据于2025-06-25公开中

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