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  2. DYRK2 - dual specificity tyrosine phosphorylation regulated kinase 2 Gene

DYRK2 - dual specificity tyrosine phosphorylation regulated kinase 2 Gene

中文名称:双特异性酪氨酸磷酸化调节激酶 2

种属: Homo sapiens

基因 ID: 8445 | 基因类型: protein coding

关于 DYRK2

Cytogenetic location: 12q15 Genomic coordinates (GRCh38): 12:67,648,745-67,665,406 (from NCBI)

This gene has 6 transcripts (splice variants), 208 orthologues and 12 paralogues. Ubiquitous expression in colon (RPKM 11.8), small intestine (RPKM 10.4) and 25 other tissues.

功能概要

DYRK2 属于蛋白激酶家族,推测其成员参与细胞生长和/或发育。该家族由其激酶结构域的结构相似性及其在酪氨酸残基上自磷酸化的能力来定义。 DYRK2 在体外证明了酪氨酸自磷酸化和组蛋白 H3 和 H2B 的催化磷酸化。已分离出两种 DYRK2 亚型。主要的亚型,亚型 1,缺少 5' 末端插入。[RefSeq 提供,2008 年 7 月]

DYRK2 belongs to a family of protein kinases whose members are presumed to be involved in cellular growth and/or development. The family is defined by structural similarity of their kinase domains and their capability to autophosphorylate on tyrosine residues. DYRK2 has demonstrated tyrosine autophosphorylation and catalyzed phosphorylation of histones H3 and H2B in vitro. Two isoforms of DYRK2 have been isolated. The predominant isoform, isoform 1, lacks a 5' terminal insert. [provided by RefSeq, Jul 2008]

DYRK2 基因产物(3)

mRNA Protein Name
XM_017020032.2 XP_016875521.1 dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform X1
NM_003583.4 NP_003574.1 dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform 1
NM_006482.3 NP_006473.2 dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform 2
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 ATP binding IDA
IDA: 通过直接分析推断
11311121 GOA
enables magnesium ion binding IDA
IDA: 通过直接分析推断
9748265 GOA
enables manganese ion binding IDA
IDA: 通过直接分析推断
9748265 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
23602568 GOA
enables protein serine/threonine kinase activity IDA
IDA: 通过直接分析推断
11311121 GOA
enables protein tyrosine kinase activity IDA
IDA: 通过直接分析推断
9748265 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in DNA damage response IEP
IEP: 通过表达模式推断
19965871 GOA
involved in intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator IDA
IDA: 通过直接分析推断
17349958 GOA
involved in negative regulation of calcineurin-NFAT signaling cascade IMP
IMP: 通过突变表型推断
16511445 GOA
involved in positive regulation of glycogen biosynthetic process IDA
IDA: 通过直接分析推断
11311121 GOA
involved in protein phosphorylation IDA
IDA: 通过直接分析推断
11311121 GOA
involved in smoothened signaling pathway IMP
IMP: 通过突变表型推断
18455992 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
17349958 GOA
located in nucleus IDA
IDA: 通过直接分析推断
17349958 GOA
part of ubiquitin ligase complex IDA
IDA: 通过直接分析推断
19287380 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

DYRK2 蛋白结构

Pkinase

Pkinase: Protein kinase domain (222 - 535)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 601 a.a.
蛋白主名 其他名称

dual specificity tyrosine-phosphorylation-regulated kinase 2

dual specificity tyrosine-(Y)-phosphorylation regulated kinase 2

DYRK2 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
DYRK2 Q92630 YWHAE Homo sapiens P62258 36931259
种属内
DYRK2 Q92630 DYRK4 Homo sapiens Q9NR20 23602568
种属内
DYRK2 Q92630 DYRK4 Homo sapiens Q9NR20
TAP
23602568
种属内
DYRK2 Q92630 ZBTB9 Homo sapiens Q96C00 25416956
种属内
DYRK2 Q92630 WDR62 Homo sapiens O43379 25416956
种属内
DYRK2 Q92630 WDR62 Homo sapiens O43379 25416956
种属内
DYRK2 Q92630 KXD1 Homo sapiens Q9BQD3 25416956
种属内
DYRK2 Q92630 LZTS2 Homo sapiens Q9BRK4 25416956
种属内
DYRK2 Q92630 LZTS2 Homo sapiens Q9BRK4 25416956
种属内
DYRK2 Q92630 SP100 Homo sapiens P23497 25416956
种属内
DYRK2 Q92630 SP100 Homo sapiens P23497 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
Waardenburg Syndrome, Type 2b

Waardenburg Syndrome Type 2b

WS2B

Waardenburg Syndrome, Type Iib

Waardenburg Syndrome Type Iib

Intellectual Developmental Disorder, Autosomal Dominant 7

MRD7

Mental Retardation, Autosomal Dominant 7

Autosomal Dominant Non-Syndromic Intellectual Disability 7

Dyrk1a Syndrome

Autosomal Dominant Intellectual Developmental Disorder 7

Autosomal Dominant Mental Retardation 7

Mental Retardation, Autosomal Dominant, Type 7

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 DYRK2 MGD MGI:1330301
Felis catus DYRK2 VGNC VGNC:61687
Bos taurus DYRK2 VGNC VGNC:55902
Rattus norvegicus DYRK2 RGD RGD:1312039
Macaca mulatta DYRK2 VGNC VGNC:72018
Canis familiaris DYRK2 VGNC VGNC:40157
Others DYRK2 NCBI