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  2. EIF2S2 - eukaryotic translation initiation factor 2 subunit beta Gene

EIF2S2 - eukaryotic translation initiation factor 2 subunit beta Gene

中文名称:真核翻译起始因子 2 亚基 beta

种属: Homo sapiens

同用名: EIF2; EIF2B; PPP1R67; EIF2beta; eIF-2-beta

基因 ID: 8894 | 基因类型: protein coding

关于 EIF2S2

Cytogenetic location: 20q11.22 Genomic coordinates (GRCh38): 20:34,088,309-34,112,243 (from NCBI)

This gene has 1 transcript (splice variant) and 253 orthologues. Ubiquitous expression in placenta (RPKM 24.2), thyroid (RPKM 22.6) and 25 other tissues.

功能概要

真核翻译起始因子 2 (EIF-2) 通过与 GTP 和起始 tRNA 形成三元复合物并与 40S 核糖体亚基结合,在蛋白质合成的早期步骤中发挥作用。 EIF-2 由 alpha、beta 和 gamma 三个亚基组成,该基因编码的蛋白质代表 beta 亚基。 β 亚基催化 GDP 与 GTP 的交换,GTP 将 EIF-2 复合物再循环用于另一轮启动。已发现该基因编码不同异构体的多个转录变体。[RefSeq 提供,2015 年 10 月]

Eukaryotic translation initiation factor 2 (EIF-2) functions in the early steps of protein synthesis by forming a ternary complex with GTP and initiator tRNA and binding to a 40S ribosomal subunit. EIF-2 is composed of three subunits, alpha, beta, and gamma, with the protein encoded by this gene representing the beta subunit. The beta subunit catalyzes the exchange of GDP for GTP, which recycles the EIF-2 complex for another round of initiation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]

EIF2S2 基因产物(3)

mRNA Protein Name
NM_001316363.2 NP_001303292.1 eukaryotic translation initiation factor 2 subunit 2 isoform 2
NM_001316364.2 NP_001303293.1 eukaryotic translation initiation factor 2 subunit 2 isoform 3
NM_003908.5 NP_003899.2 eukaryotic translation initiation factor 2 subunit 2 isoform 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
11959995 GOA
enables translation initiation factor activity IDA
IDA: 通过直接分析推断
16289705 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cytoplasmic translational initiation IMP
IMP: 通过突变表型推断
31836389 GOA
involved in translational initiation IDA
IDA: 通过直接分析推断
10563826 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
12426392 GOA
part of eukaryotic translation initiation factor 2 complex IDA
IDA: 通过直接分析推断
23063529 GOA
part of eukaryotic translation initiation factor 2 complex IPI
IPI: 通过物理相互作用推断
31836389 GOA
NOT located in nucleus IDA
IDA: 通过直接分析推断
12426392 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

EIF2S2 蛋白结构

eIF-5_eIF-2B

eIF-5_eIF-2B: Domain found in IF2B/IF5 (189 - 309)

  • 0
  • 100
  • 200
  • 300
  • 333 a.a.
蛋白主名 其他名称

eukaryotic translation initiation factor 2 subunit 2

eukaryotic translation initiation factor 2, subunit 2 beta, 38kDa

EIF2S2 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
Intra EIF2S2 P20042 NGF Homo sapiens P01138
Validated Y2H
32814053
Intra EIF2S2 P20042 NGF Homo sapiens P01138
Y2H Pooling
32814053
Intra EIF2S2 P20042 NGF Homo sapiens P01138
Y2H Array
32814053
Intra EIF2S2 P20042 EIF2S3 Homo sapiens P41091
Anti Tag CoIP
33961781
Intra EIF2S2 P20042 EIF2S3 Homo sapiens P41091
ELISA
16288713
Intra EIF2S2 P20042 EIF2S3 Homo sapiens P41091
Anti Tag CoIP
28514442
Intra EIF2S2 P20042 EIF2S1 Homo sapiens P05198
Anti Tag CoIP
28514442
Intra EIF2S2 P20042 EIF2S1 Homo sapiens P05198
ELISA
16288713
Intra EIF2S2 P20042 EIF2S1 Homo sapiens P05198
Anti Tag CoIP
33961781
Intra EIF2S2 P20042 SORL1 Homo sapiens Q92673
Y2H Array
32814053
Intra EIF2S2 P20042 SORL1 Homo sapiens Q92673
Y2H Pooling
32814053
Intra EIF2S2 P20042 SORL1 Homo sapiens Q92673
Validated Y2H
32814053
Intra EIF2S2 P20042 CDC123 Homo sapiens O75794
Anti Tag CoIP
33961781
Intra EIF2S2 P20042 CDC123 Homo sapiens O75794
Anti Tag CoIP
28514442
Intra EIF2S2 P20042 EIF4G2 Homo sapiens P78344
Pull Down
16932749
Intra EIF2S2 P20042 EIF4G2 Homo sapiens P78344
Anti Tag CoIP
16932749
Intra EIF2S2 P20042 KAT5 Homo sapiens Q92993
Y2H Pooling
32814053
Intra EIF2S2 P20042 KAT5 Homo sapiens Q92993
Validated Y2H
32814053
Intra EIF2S2 P20042 KAT5 Homo sapiens Q92993
Y2H Array
32814053
Intra EIF2S2 P20042 HTT Homo sapiens P42858
Validated Y2H
32814053
Intra EIF2S2 P20042 HTT Homo sapiens P42858
Y2H Array
32814053
Intra EIF2S2 P20042 HTT Homo sapiens P42858
Y2H Pooling
32814053
Intra EIF2S2 P20042 MAP3K5 Homo sapiens Q99683
Y2H Array
32814053
Intra EIF2S2 P20042 MAP3K5 Homo sapiens Q99683
Validated Y2H
32814053
Intra EIF2S2 P20042 MAP3K5 Homo sapiens Q99683
Y2H Pooling
32814053
Intra EIF2S2 P20042 PMP22 Homo sapiens A0A6Q8PF08
Y2H Pooling
32814053
Intra EIF2S2 P20042 PMP22 Homo sapiens A0A6Q8PF08
Validated Y2H
32814053
Intra EIF2S2 P20042 PMP22 Homo sapiens A0A6Q8PF08
Y2H Array
32814053
Intra EIF2S2 P20042 CHRNA4 Homo sapiens P43681
Validated Y2H
32814053
Intra EIF2S2 P20042 CHRNA4 Homo sapiens P43681
Y2H Array
32814053
Intra EIF2S2 P20042 CHRNA4 Homo sapiens P43681
Y2H Pooling
32814053
Intra EIF2S2 P20042 ATXN1 Homo sapiens P54253
Validated Y2H
32814053
Intra EIF2S2 P20042 ATXN1 Homo sapiens P54253
Y2H Array
32814053
Intra EIF2S2 P20042 ATXN1 Homo sapiens P54253
Y2H Pooling
32814053
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Leukoencephalopathy With Vanishing White Matter

Cree Leukoencephalopathy

Vanishing White Matter Disease

Ovarioleukodystrophy

Vanishing White Matter Leukodystrophy

Childhood Ataxia With Central Nervous System Hypomyelinization

Cach

Cach Syndrome

Myelinosis Centralis Diffusa

VWM

Cle

Childhood Ataxia With Central Nervous System Hypomyelination

Childhood Ataxia With Diffuse Central Nervous System Hypomyelination

Cach/Vwm

Cach/Vwm Syndrome

Childhood Ataxia With Central Nervous System Hypomyelination/Vanishing White Matter

Cree Leukoencehalopathy

Late Infantile Cach Syndrome

Juvenile Or Adult Cach Syndrome

Congenital Or Early Infantile Cach Syndrome

Leukodystrophy With Vanishing White Matter

Mehmo Syndrome

Mental Retardation, Epileptic Seizures, Hypogonadism And Hypogenitalism, Microcephaly, And Obesity

MEHMO

Mrxs20

Mrxs25

X-Linked Intellectual Disability-Epileptic Seizures-Hypogenitalism-Microcephaly-Obesity Syndrome

Mrxsbrk

Mental Retardation, X-Linked, Syndromic 20

Mental Retardation, X-Linked, Syndromic 25

Mental Retardation, X-Linked, Syndromic, Borck Type

Syndromic X-Linked Mental Retardation 20

Syndromic X-Linked Mental Retardation 25

Intellectual Disability, Epileptic Seizures, Hypogonadism And Hypogenitalism, Microcephaly, And Obesity

X-Linked Mehmo 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
Rattus norvegicus EIF2S2 RGD RGD:735192
Felis catus EIF2S2 VGNC VGNC:61779
Mus musculus EIF2S2 MGD MGI:1914454
Macaca mulatta EIF2S2 VGNC VGNC:84912
Bos taurus EIF2S2 VGNC VGNC:28391
Canis familiaris EIF2S2 VGNC VGNC:40267