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Immunogen sequence: CKKSGQSYSP SRVLITENDV KEGLQRSHIL YDRAGEEHYN CISALHKSMR GSDQNASLYW LARMLEGGED PLYVARRLVR FAS
Highest antigen sequence identity to the following orthologs: Mouse - 98%, Rat - 98%.
Werner's syndrome is a rare autosomal recessive disorder characterized by accelerated aging that is caused by defects in the Werner syndrome ATP-dependent helicase gene (WRN). The protein encoded by this gene interacts with the exonuclease-containing N-terminal portion of the Werner protein. This protein has a ubiquitin-binding zinc-finger domain in the N-terminus, an ATPase domain, and two leucine zipper motifs in the C-terminus. It has sequence similarity to replication factor C family proteins and is conserved from E. coli to human. This protein likely accumulates at sites of DNA damage by interacting with polyubiquinated proteins and also binds to DNA polymerase delta and increases the initiation frequency of DNA polymerase delta-mediated DNA synthesis. This protein also interacts with nucleoporins at nuclear pore complexes. Two transcript variants encoding different isoforms have been isolated for this gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: ATPase WRNIP1; FLJ22526; putative helicase RUVBL; RP11-420G6.2; Werner helicase-interacting protein 1; WRNIP1
基因别名: bA420G6.2; WHIP; WRNIP1
UniProt ID: (Human) Q96S55
Entrez Gene ID: (Human) 56897