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ZC3HAV1 (基因名), Zinc finger CCCH-type antiviral protein 1 (蛋白名), zcchv_human.
产品名称:

Human ZC3HAV1/ Zinc finger CCCH-type antiviral protein 1 Recombinant Protein

货号:

R16041h

商标:
EIAab®
监管等级:
别名:

ADP-ribosyltransferase diphtheria toxin-like 13, Inactive Poly [ADP-ribose] polymerase 13, Zinc finger CCCH domain-containing protein 2, Zinc finger antiviral protein, ARTD13, PARP13, ZAP, PRO1677, ZC3HDC2

序列号:
Q7Z2W4
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Epigenetics
Human ZC3HAV1 Protein
规格 & 价格: cart
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Human ZC3HAV1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
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R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 7q34 by HGNC 7q34 by Entrez Gene 7q34 by Ensembl
ZC3HAV1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Homodimer or homooligomer. Homooligomerization is essential for its antiviral activity. Interacts with EXOSC5 (By similarity). Interacts (via N-terminal domain) with DDX17 in an RNA-independent manner (By similarity). Interacts with EXOSC3, EXOSC7, DCP2 and DCP1A. Interacts with PARN in an RNA-independent manner. Interacts with XRN1 in an RNA-dependent manner. Isoform 2 interacts (via zinc-fingers) with DDX58/RIG-I in an RNA-dependent manner. Interacts (via N-terminal domain) with DHX30 (via N-terminus) in an RNA-independent manner.


功能:
Antiviral protein which inhibits the replication of viruses by recruiting the cellular RNA degradation machineries to degrade the viral mRNAs. Binds to a ZAP-responsive element (ZRE) present in the target viral mRNA, recruits cellular poly(A)-specific ribonuclease PARN to remove the poly(A) tail, and the 3'-5' exoribonuclease complex exosome to degrade the RNA body from the 3'-end. It also recruits the decapping complex DCP1-DCP2 through RNA helicase p72 (DDX17) to remove the cap structure of the viral mRNA to initiate its degradation from the 5'-end. Its target viruses belong to families which include retroviridae: human immunodeficiency virus type 1 (HIV-1), moloney and murine leukemia virus (MoMLV) and xenotropic MuLV-related virus (XMRV), filoviridae: ebola virus (EBOV) and marburg virus (MARV), togaviridae: sindbis virus (SINV) and Ross river virus (RRV). Specifically targets the multiply spliced but not unspliced or singly spliced HIV-1 mRNAs for degradation. Isoform 1 is a more potent viral inhibitor than isoform 2. Isoform 2 acts as a positive regulator of DDX58/RIG-I signaling resulting in activation of the downstream effector IRF3 leading to the expression of type I IFNs and IFN stimulated genes (ISGs).


亚细胞位置:
Isoform 2 Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Structural basis for lack of ADP-ribosyltransferase activity in poly(ADP-ribose) polymerase-13/zinc finger antiviral protein."

[2].
"Positive selection and increased antiviral activity associated with the PARP-containing isoform of human zinc-finger antiviral protein."

[3].
"Identification and characterization of human TIPARP gene within the CCNL amplicon at human chromosome 3q25.31."

[4].
"Inhibition of retroviral RNA production by ZAP, a CCCH-type zinc finger protein."

[5].
"Family-wide analysis of poly(ADP-ribose) polymerase activity."

[6].
"ZAPS is a potent stimulator of signaling mediated by the RNA helicase RIG-I during antiviral responses."

[7].
"Zinc-finger antiviral protein inhibits HIV-1 infection by selectively targeting multiply spliced viral mRNAs for degradation."

[8].
"Expression and RNA-binding of human zinc-finger antiviral protein."

[9].
"DEXH-Box protein DHX30 is required for optimal function of the zinc-finger antiviral protein."

[10].
"ZAP-mediated mRNA degradation."
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