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716 C1S

716

C1S

complement C1s

protein-coding

Homo sapiens

基因描述

Type Description
Definition complement C1s

研究结论

Date Results Publications
2020-11-21 13:24:00 Two Different Missense C1S Mutations, Associated to Periodontal Ehlers-Danlos Syndrome, Lead to Identical Molecular Outcomes. 31921203
2018-05-12 10:18:00 The serine protease domains of C1r and C1s are at the periphery of the C1r2s2 tetramer both when alone or within the nonactivated C1 complex. The C1 complex adopts a conformation incompatible with intramolecular activation of C1. Instead, intermolecular proteolytic activation between neighboring C1 complexes bound to a complement-activating surface occurs. Many structurally unrelated molecular patterns can activate C1. 28104818
2017-05-20 12:27:00 Periodontal Ehlers-Danlos Syndrome in at least the great majority of cases results from specific classes of heterozygous mutations in C1R and C1S. 27745832
2015-12-05 10:26:00 C1q exists as the C1 complex (C1qC1r2C1s2), and C1q binding to ligands activates the C1r/C1s proteases. Incubation of nucleoli with C1 caused degradation of the nucleolar proteins nucleolin and nucleophosmin 1. T 26231209
2014-09-06 12:19:00 TNT003, an inhibitor of the serine protease C1s, prevents complement activation induced by cold agglutinins. 24695853

名称对应

Type IDs
Synonymous EDSPD2
Gene
UniProtKB-ID: C1S_HUMAN, F8WCZ6_HUMAN
UniprotKB: P09871, F8WCZ6
UniParc: UPI000022932D, UPI0000126BF6
EMBL: J04080, AB009076, BC056903, CH471116, X06596, M18767, AC006512
Ensembl: ENSG00000182326
KO: hsa:716
Nucleutide sequences
EMBL-CDS: AAA51852.1, EAW88689.1, CAA29817.1, AAH56903.1, BAA86864.1, EAW88690.1, AAA51853.1
Ensembl_TRS: ENST00000328916, ENST00000406697, ENST00000360817, ENST00000402681
Protein sequencees
Ensembl_PRO: ENSP00000385035, ENSP00000354057, ENSP00000328173, ENSP00000384171
RefSeq: NP_001725.1, XP_005253817.1, NP_001333779.1, NP_958850.1
Others
UniRef100: UniRef100_P09871
UniRef90: UniRef90_P09871
UniRef50: UniRef50_P09871
UniGene: Hs.458355
CCDS: CCDS31735.1

全选

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