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  2. EIF4EBP2 - eukaryotic translation initiation factor 4E binding protein 2 Gene

EIF4EBP2 - eukaryotic translation initiation factor 4E binding protein 2 Gene

中文名称:真核翻译起始因子 4E 结合蛋白 2

种属: Homo sapiens

同用名: 4EBP2; PHASII

基因 ID: 1979 | 基因类型: protein coding

关于 EIF4EBP2

Cytogenetic location: 10q22.1 Genomic coordinates (GRCh38): 10:70,404,145-70,428,618 (from NCBI)

This gene has 1 transcript (splice variant), 205 orthologues and 2 paralogues. Ubiquitous expression in fat (RPKM 50.2), kidney (RPKM 34.8) and 25 other tissues.

功能概要

该基因编码真核翻译起始因子 4E 结合蛋白家族的成员。该家族的基因产物结合 eIF4E 并抑制翻译起始。然而,胰岛素和其他生长因子可以通过磷酸化依赖性破坏它们与 eIF4E 的结合来释放这种抑制作用。通过这些基因产物调节蛋白质生产与细胞增殖、细胞分化和病毒感染有关。[RefSeq 提供,2008 年 10 月]

This gene encodes a member of the eukaryotic translation initiation factor 4E binding protein family. The gene products of this family bind eIF4E and inhibit translation initiation. However, Insulin and Other growth factors can release this inhibition via a phosphorylation-dependent disruption of their binding to eIF4E. Regulation of protein production through these gene products have been implicated in cell proliferation, cell differentiation and viral Infection. [provided by RefSeq, Oct 2008]

EIF4EBP2 基因产物(1)

mRNA Protein Name
NM_004096.5 NP_004087.1 eukaryotic translation initiation factor 4E-binding protein 2

EIF4EBP2 蛋白结构

eIF_4EBP

eIF_4EBP: Eukaryotic translation initiation factor 4E binding protein (EIF4EBP) (8 - 120)

  • 0
  • 100
  • 120 a.a.
蛋白主名 其他名称

eukaryotic translation initiation factor 4E-binding protein 2

4E-BP2

EIF4EBP2 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
EIF4EBP2 Q13542 EIF4E Homo sapiens P06730
NMR
24207126
种属内
EIF4EBP2 Q13542 EIF4E Homo sapiens P06730
Y2H Prey Pooling
25416956
种属内
EIF4EBP2 Q13542 EIF4E Homo sapiens P06730
ITC
24207126
种属内
EIF4EBP2 Q13542 EIF4E Homo sapiens P06730
Validated Y2H
25416956
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 EIF4EBP2 蛋白

目录号 产品名 蛋白编号 纯度
HY-P70416 EIF4EBP2 Protein, Human (His) Q13542 (M1-I120) ≥95%

关联疾病

疾病名称 别名
Fragile X Syndrome

FXS

Martin-Bell Syndrome

Fraxa Syndrome

Marker X Syndrome

X-Linked Mental Retardation And Macroorchidism

Fragile X Mental Retardation Syndrome

Fra Syndrome

Mental Retardation, X-Linked, Associated With Marxq28

X-Linked Intellectual Disability And Macroorchidism

Frax Syndrome

Symptomatic Form Of Fragile X Syndrome In Female Carriers

Fragile-X Syndrome

Fraxe Syndrome

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Bos taurus EIF4EBP2 VGNC VGNC:28413
Canis familiaris EIF4EBP2 VGNC VGNC:40287
Mus musculus EIF4EBP2 MGD MGI:109198
Rattus norvegicus EIF4EBP2 RGD RGD:1310824
Macaca mulatta EIF4EBP2 VGNC VGNC:106043
Others EIF4EBP2 NCBI