
KREMEN1 - Wikipedia
Kremen protein 1 is a protein that in humans is encoded by the KREMEN1 gene. [5][6] Kremen1 is conserved in chordates including amphioxus [7] and most vertebrate species. [8] The …
Receptome profiling identifies KREMEN1 and ASGR1 as …
2021年11月26日 · Our study revealed an interacting host receptome of SARS-CoV-2, and identified ASGR1 and KREMEN1 as alternative functional receptors that play essential roles in …
KREMEN1 Gene - GeneCards | KREM1 Protein | KREM1 Antibody
2025年3月30日 · Complete information for KREMEN1 gene (Protein Coding), Kringle Containing Transmembrane Protein 1, including: function, proteins, disorders, pathways, orthologs, and …
新冠病毒有其他受体(2):Kremen-1 - 知乎专栏
Kremen-1和Kremen-2(属于 I型跨膜蛋白)又是能够与Dkk蛋白特异性结合的跨膜蛋白——确切地讲是Dkk1和Dkk2,是继Lrp5, 6以后第二组被发现的Dkk受体,并且较前者而言亲和力更高。 …
KREMEN1 Is a Host Entry Receptor for a Major Group of ... - PubMed
2018年5月9日 · We identify the cell surface molecule KREMEN1 as an entry receptor for coxsackievirus A10 (CV-A10). Whereas loss of KREMEN1 renders cells resistant to CV-A10 …
Hand-foot-and-mouth disease virus receptor KREMEN1 binds …
2020年1月7日 · KREMEN1 (KRM1) is the entry receptor for the largest receptor-group of hand-foot-and-mouth disease causing viruses, which includes CV-A10. We report here structures of …
含 Kringle 跨膜蛋白 1(KREMEN1)基因 | MCE
该基因编码高亲和力的 dickkopf 同系物 1 (DKK1) 跨膜受体,该受体在功能上与 DKK1 协同阻断无翼 (Wnt) /β-连环蛋白信号传导。 编码的蛋白质是膜复合物的一个组成部分,它通过脂蛋白受 …
Novel SARS-CoV-2 receptors: ASGR1 and KREMEN1 - Nature
2021年12月13日 · ASGR1- and KREMEN1-specific antibodies blocked S protein binding and entry into cell lines and reduced infection of lung organoids, suggesting a role for these factors …
KREMEN1 kringle containing transmembrane protein 1
2025年2月8日 · Gene ID: 83999, updated on 8-Feb-2025. This gene encodes a high-affinity dickkopf homolog 1 (DKK1) transmembrane receptor that functionally cooperates with DKK1 …
Structure of the Dual-Mode Wnt Regulator Kremen1 and Insight …
Kremen 1 and 2 have been identified as co-receptors for Dickkopf (Dkk) proteins, hallmark secreted antagonists of canonical Wnt signaling. We present here three crystal structures of …