1. Gene
  2. ATP4B - ATPase H+/K+ transporting subunit beta Gene

ATP4B - ATPase H+/K+ transporting subunit beta Gene

中文名称:ATPase H+/K+ 转运亚基 β

种属: Homo sapiens

同用名: ATP6B

基因 ID: 496 | 基因类型: protein coding

关于 ATP4B

Cytogenetic location: 13q34 Genomic coordinates (GRCh38): 13:113,648,804-113,658,198 (from NCBI)

This gene has 1 transcript (splice variant), 1 gene allele, 171 orthologues and 4 paralogues. Restricted expression toward stomach (RPKM 286.6).

功能概要

该基因编码的蛋白质属于 P 型阳离子转运 ATP 酶家族。胃 H+、K+-ATP 酶是一种异二聚体,由一个高分子量催化性 α 亚基和一个较小但高度糖基化的 β 亚基组成。这种酶是一种质子泵,可催化 ATP 的水解以及质膜上 H (+) 和 K (+) 离子的交换。它还负责胃酸分泌。该基因编码胃 H+、K+-ATP 酶的 β 亚基。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene belongs to a family of P-type cation-transporting ATPases. The gastric H+, K+-ATPase is a heterodimer consisting of a high molecular weight catalytic alpha subunit and a smaller but heavily glycosylated beta subunit. This Enzyme is a Proton Pump that catalyzes the hydrolysis of ATP coupled with the exchange of H(+) and K(+) ions across the plasma membrane. It is also responsible for gastric acid secretion. This gene encodes the beta subunit of the gastric H+, K+-ATPase. [provided by RefSeq, Jul 2008]

ATP4B 基因产物(1)

mRNA Protein Name
NM_000705.4 NP_000696.1 potassium-transporting ATPase subunit beta
基因本体论
  • 分子功能
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
25416956 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

ATP4B 蛋白结构

Na_K-ATPase

Na_K-ATPase: Sodium / potassium ATPase beta chain (1 - 286)

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

potassium-transporting ATPase subunit beta

ATPase H+/K+ transporting beta subunit

ATP4B 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 ATP4B P51164 GPR42 Homo sapiens O15529
Y2H Prey Pooling
32296183
Intra ATP4B P51164 GPR42 Homo sapiens O15529
Y2H Array
32296183
Intra ATP4B P51164 ZC4H2 Homo sapiens Q9NQZ6
Validated Y2H
32296183
Intra ATP4B P51164 ZC4H2 Homo sapiens Q9NQZ6
Y2H Array
32296183
Intra ATP4B P51164 ZC4H2 Homo sapiens Q9NQZ6
Y2H Prey Pooling
32296183
Intra ATP4B P51164 CCNDBP1 Homo sapiens O95273
Y2H Array
25416956
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
Chronic Laryngitis
Myasthenic Syndrome, Congenital, 11, Associated With Acetylcholine Receptor Deficiency

Congenital Myasthenic Syndrome 11

CMS11

Cms Ie

Cms1e

Myasthenic Syndrome, Congenital, Ie

Myasthenic Syndrome, Congenital, Ie, Formerly

Cms1e, Formerly

Cms Ie, Formerly

Congenital Myasthenic Syndrome 11 Associated With Acetylcholine Receptor Deficiency

Congenital Myasthenic Syndrome 1e

Myasthenic Syndrome, Congenital, Type 11, Associated With Acetylcholine Receptor Deficiency

Autoimmune Gastritis
Brain Small Vessel Disease 2

Porencephaly 2

BSVD2

Gould Syndrome 2

Porencephaly 2, Formerly

Poren2, Formerly

Poren2

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
Macaca mulatta ATP4B VGNC VGNC:106251
Rattus norvegicus ATP4B RGD RGD:2178
Bos taurus ATP4B VGNC VGNC:26298
Felis catus ATP4B VGNC VGNC:68642
Mus musculus ATP4B MGD MGI:88114
Canis familiaris ATP4B VGNC VGNC:38263