1. Gene
  2. ATP5PB - ATP synthase peripheral stalk-membrane subunit b Gene

ATP5PB - ATP synthase peripheral stalk-membrane subunit b Gene

中文名称:ATP 合酶外周茎膜亚基 b

种属: Homo sapiens

同用名: PIG47; ATP5F1

基因 ID: 515 | 基因类型: protein coding

关于 ATP5PB

Cytogenetic location: 1p13.2 Genomic coordinates (GRCh38): 1:111,449,464-111,462,773 (from NCBI)

This gene has 6 transcripts (splice variants) and 266 orthologues. Ubiquitous expression in heart (RPKM 107.3), colon (RPKM 76.0) and 25 other tissues.

功能概要

该基因编码线粒体 ATP 合酶的一个亚基。线粒体 ATP 合酶催化 ATP 合成,利用氧化磷酸化过程中跨内膜的质子电化学梯度。 ATP 合酶由两个连接的多亚基复合物组成:可溶性催化核心 F1 和跨膜成分 Fo,构成质子通道。线粒体 ATP 合酶的催化部分由 5 个不同的亚基 (alpha、beta、gamma、delta 和 epsilon) 组成,其化学计量为 3 个 alpha、3 个 beta 和其他 3 个的单一代表。质子通道似乎具有九个亚基 (a、b、c、d、e、f、g、F6 和 8) 。该基因编码质子通道的 b 亚基。[RefSeq 提供,2008 年 7 月]

This gene encodes a subunit of mitochondrial ATP Synthase. Mitochondrial ATP Synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during Oxidative Phosphorylation. ATP Synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP Synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the Other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the b subunit of the proton channel. [provided by RefSeq, Jul 2008]

ATP5PB 基因产物(1)

mRNA Protein Name
NM_001688.5 NP_001679.2 ATP synthase F(0) complex subunit B1, mitochondrial precursor
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
19016746 GOA
contributes to proton-transporting ATP synthase activity, rotational mechanism IDA
IDA: 通过直接分析推断
12110673 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in proton motive force-driven mitochondrial ATP synthesis IDA
IDA: 通过直接分析推断
12110673 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of proton-transporting ATP synthase complex IDA
IDA: 通过直接分析推断
12110673 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

ATP5PB 蛋白结构

Mt_ATP-synt_B

Mt_ATP-synt_B: Mitochondrial ATP synthase B chain precursor (ATP-synt_B) (83 - 244)

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

ATP synthase F(0) complex subunit B1, mitochondrial

ATP synthase B chain, mitochondrial

ATP5PB 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
ATP5PB P24539 DELE1 Homo sapiens Q14154 32814053
种属内
ATP5PB P24539 DELE1 Homo sapiens Q14154 32814053
种属内
ATP5PB P24539 DELE1 Homo sapiens Q14154 32814053
种属内
ATP5PB P24539 ATP5F1A Homo sapiens P25705 19688755
种属内
ATP5PB P24539 ATP5F1A Homo sapiens P25705 33961781
种属内
ATP5PB P24539 ATP5F1A Homo sapiens P25705 28514442
种属内
ATP5PB P24539 ATP5F1A Homo sapiens P25705 30021884
种属内
ATP5PB P24539 HTT Homo sapiens P42858 32814053
种属内
ATP5PB P24539 HTT Homo sapiens P42858 32814053
种属内
ATP5PB P24539 HTT Homo sapiens P42858 32814053
种属内
ATP5PB P24539 ATP5PD Homo sapiens O75947 33961781
种属内
ATP5PB P24539 ATP5PD Homo sapiens O75947 19688755
种属内
ATP5PB P24539 METTL27 Homo sapiens Q8N6F8 32814053
种属内
ATP5PB P24539 METTL27 Homo sapiens Q8N6F8 32814053
种属内
ATP5PB P24539 METTL27 Homo sapiens Q8N6F8 32814053
种属内
ATP5PB P24539 ATXN1 Homo sapiens P54253 32814053
种属内
ATP5PB P24539 ATXN1 Homo sapiens P54253 32814053
种属内
ATP5PB P24539 ATXN1 Homo sapiens P54253 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
Amyotrophic Lateral Sclerosis 1

Amyotrophic Lateral Sclerosis

ALS

Lou Gehrig Disease

Amyotrophic Lateral Sclerosis Type 1

Charcot Disease

ALS1

Amyotrophic Lateral Sclerosis, Susceptibility To

Fals

Lou Gehrig'S Disease

Mnd

Motor Neuron Disease

Familial Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis 1, Familial

Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

Motor Neuron Disease, Bulbar

Motor Neurone Disease

Amyotrophic Lateral Sclerosis With Dementia

Dementia With Amyotrophic Lateral Sclerosis

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Sclerosis, Lateral, Amyotrophic

Sclerosis, Lateral, Amyotrophic, Type 1

Amyotrophic Sclerosis

Als - [Amyotrophic Lateral Sclerosis]

Wasting Palsy

Amyotrophic Paralysis

Amyotrophy Lateral Sclerosis

Wasting Paralysis

Spinal Progressive Amyotrophy

Progressive Atrophic Paralysis

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
Mus musculus ATP5PB MGD MGI:1100495
Bos taurus ATP5PB VGNC VGNC:26303
Rattus norvegicus ATP5PB RGD RGD:620041
Felis catus ATP5PB VGNC VGNC:80146