1. Gene
  2. PYGB - glycogen phosphorylase B Gene

PYGB - glycogen phosphorylase B Gene

中文名称:糖原磷酸化酶 B

种属: Homo sapiens

同用名: GPBB

基因 ID: 5834 | 基因类型: protein coding

关于 PYGB

Cytogenetic location: 20p11.21 Genomic coordinates (GRCh38): 20:25,248,085-25,298,012 (from NCBI)

This gene has 3 transcripts (splice variants), 176 orthologues and 2 paralogues. Broad expression in colon (RPKM 67.8), heart (RPKM 66.8) and 23 other tissues.

功能概要

由该基因编码的蛋白质是一种主要存在于大脑中的糖原磷酸化酶。编码的蛋白质形成同型二聚体,可以结合成同型四聚体,即糖原磷酸化酶的酶促活性形式。这种酶的活性受 AMP 的正向调节,受 ATP、ADP 和葡萄糖-6-磷酸的负向调节。该酶催化糖原降解中的决速步骤。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene is a glycogen phosphorylase found predominantly in the brain. The encoded protein forms homodimers which can associate into homotetramers, the enzymatically active form of glycogen phosphorylase. The activity of this Enzyme is positively regulated by AMP and negatively regulated by ATP, ADP, and glucose-6-phosphate. This Enzyme catalyzes the rate-determining step in glycogen degradation. [provided by RefSeq, Jul 2008]

PYGB 基因产物(1)

mRNA Protein Name
NM_002862.4 NP_002853.2 glycogen phosphorylase, brain form
基因本体论
  • 分子功能
  • 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
25416956 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
10638593 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

PYGB 蛋白结构

Phosphorylase

Phosphorylase: Carbohydrate phosphorylase (112 - 830)

  • 0
  • 200
  • 400
  • 600
  • 843 a.a.
蛋白主名 其他名称

glycogen phosphorylase, brain form

phosphorylase, glycogen

PYGB 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
PYGB P11216 PYGL Homo sapiens P06737 25416956
种属内
PYGB P11216 PYGL Homo sapiens P06737 33961781
种属内
PYGB P11216 PYGL Homo sapiens P06737 25416956
种属内
PYGB P11216 PYGL Homo sapiens P06737 25416956
种属内
PYGB P11216 FKBP5 Homo sapiens Q13451 30021884
种属内
PYGB P11216 PYGM Homo sapiens P11217 33961781
种属内
PYGB P11216 PYGM Homo sapiens P11217 32296183
种属内
PYGB P11216 PYGM Homo sapiens P11217 32296183
种属内
PYGB P11216 PYGM Homo sapiens P11217 32296183
种属内
PYGB P11216 PPP1R3B Homo sapiens Q86XI6 32296183
种属内
PYGB P11216 PPP1R3B Homo sapiens Q86XI6 33961781
种属内
PYGB P11216 PPP1R3B Homo sapiens Q86XI6 32296183
种属内
PYGB P11216 PPP1R3B Homo sapiens Q86XI6 32296183
种属内
PYGB P11216 SIAH1 Homo sapiens Q8IUQ4 25416956
种属内
PYGB P11216 SIAH1 Homo sapiens Q8IUQ4 25416956
种属内
PYGB P11216 SIAH1 Homo sapiens Q8IUQ4 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
Glycogen Storage Disease Vi

Glycogen Storage Disease Type Vi

Hers Disease

GSD6

Gsd Vi

Hepatic Glycogen Phosphorylase Deficiency

Phosphorylase Deficiency Glycogen-Storage Disease Of Liver

Hers' Disease

Glycogen Storage Disease Type 6

Glycogen Storage Disease 6

Gsd Type Vi

Glycogenosis Type Vi

Glycogen Storage Disease, Type Vi

Hepatophosphorylase Deficiency Glycogenosis

Liver Phosphorylase Deficiency Syndrome

Glycogen Storage Disease Due To Liver Glycogen Phosphorylase Deficiency

Gsd Due To Liver Glycogen Phosphorylase Deficiency

Gsd Type 6

Glycogenosis Due To Liver Glycogen Phosphorylase Deficiency

Glycogenosis Type 6

Hepatic Phosphorylase Deficiency

Liver Glycogen Phosphorylase Deficiency

Her

Glycogen Storage Disease Vib

Gsd-Vi

Liver Phosphorylase Deficiency

Storage Disease, Glycogen, Type Vi

Glycogen Storage Disease Viii

Glycogen Storage Disease Type Viii

Glycogenosis Type Viii

Glycogen Storage Disease 8

Hepatic Glycogen Phosphorylase Kinase Deficiency

Glycogenosis Type 8

Hepatic Phosphorylase Kinase Deficiency

Pykl

Phosphorylase Kinase Deficiency Of Liver

Glycogen Storage Disease, Type Ix

Glycogen Storage Disease V

Mcardle Disease

Myophosphorylase Deficiency

Glycogen Storage Disease Type V

Muscle Glycogen Phosphorylase Deficiency

Pygm Deficiency

Gsd V

Glycogen Storage Disease, Type V

Glycogenosis Type V

Glycogen Storage Disease Type 5

GSD5

Pygmy

Mcardle'S Disease

Mcardle Type Glycogen Storage Disease

Gsd Type V

Pygmy, African

Gsdv

Gsd 5

Glycogenosis 5

Mcardle Syndrome

Muscle Phosphorylase Deficiency

Glycogen Storage Disease Due To Muscle Glycogen Phosphorylase Deficiency

Gsd Due To Muscle Glycogen Phosphorylase Deficiency

Gsd Type 5

Glycogenosis Due To Muscle Glycogen Phosphorylase Deficiency

Glycogenosis Type 5

Glycogen Storage Disease 5

Gsd-V

Mcardles Disease

Storage Disease, Glycogen, Type V

Glycogen Storage Disease Ixa

Glycogen Storage Disease Type 9a

Glycogen Storage Disease Type Ixa

Glycogenosis Type 9a

Glycogenosis Type Ixa

Gsd Type 9a

Gsd Type Ixa

Gsd9a

Myocardial Infarction

Heart Attack

Myocardial Infarction, Susceptibility To

Myocardial Infarction 1

Myocardial Infarction, Protection Against

Myocardial Infarction, Decreased Susceptibility To

Myocardial Infarction, Decreased

Myocardial Infarct

MCI1

Premature Myocardial Infarction

Myocardial Infarction, Susceptibility To, Type 1

Myoclonic Epilepsy Of Lafora

Lafora Disease

Epilepsy, Progressive Myoclonic 2b

EPM2

Melf

Epilepsy, Progressive Myoclonic 2a

Epm2a

Lafora'S Disease

Lafora Body Disease

Lbd

Epilepsy, Progressive Myoclonic, 2a

Lafora Progressive Myoclonic Epilepsy

Epilepsy Progressive Myoclonic 2

Lafora Body Disorder

Pme Type 2

Progressive Myoclonic Epilepsy Type 2

Progressive Myoclonus Epilepsy Type 2

Epilepsy, Progressive Myoclonic 2

Epm2b

Ld

Progressive Myoclonic Epilepsy 2

Progressive Myoclonic Epilepsy 2a

Progressive Myoclonic Epilepsy 2b

Progressive Myoclonic Epilepsy Lafora Type

Epilepsy, Myoclonic, Of Lafora

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 PYGB MGD MGI:97828
Rattus norvegicus PYGB RGD RGD:3460
Felis catus PYGB VGNC VGNC:69192
Bos taurus PYGB VGNC VGNC:57019
Canis familiaris PYGB VGNC VGNC:52899
Macaca mulatta PYGB VGNC VGNC:76631