1. Gene
  2. CYTH3 - cytohesin 3 Gene

CYTH3 - cytohesin 3 Gene

中文名称:细胞粘附素 3

种属: Homo sapiens

同用名: GRP1; ARNO3; PSCD3; cytohesin-3

基因 ID: 9265 | 基因类型: protein coding

关于 CYTH3

Cytogenetic location: 7p22.1 Genomic coordinates (GRCh38): 7:6,161,779-6,272,624 (from NCBI)

This gene has 11 transcripts (splice variants), 293 orthologues and 15 paralogues. Ubiquitous expression in placenta (RPKM 22.7), fat (RPKM 21.0) and 23 other tissues.

功能概要

该基因编码 PSCD (pleckstrin 同源性、Sec7 和卷曲螺旋结构域) 家族的成员。 PSCD 家族成员具有相同的结构组织,由 N 末端卷曲螺旋基序、中央 Sec7 结构域和 C 末端 pleckstrin 同源 (PH) 结构域组成。卷曲螺旋基序参与同源二聚化,Sec7 结构域包含鸟嘌呤核苷酸交换蛋白 (GEP) 活性,PH 结构域与磷脂相互作用并负责 PSCD 与膜的结合。该家族的成员似乎调节蛋白质分选和膜运输的调节。这种编码的蛋白质参与高尔基体结构和功能的控制,除了作用于 ARF1 外,它还可能在调节 ADP-核糖基化因子蛋白 6 (ARF) 功能方面发挥生理作用。[RefSeq 提供,2008 年 7 月]

This gene encodes a member of the PSCD (pleckstrin homology, Sec7 and coiled-coil domains) family. PSCD family members have identical structural organization that consists of an N-terminal coiled-coil motif, a central Sec7 domain, and a C-terminal pleckstrin homology (PH) domain. The coiled-coil motif is involved in homodimerization, the Sec7 domain contains guanine-nucleotide exchange protein (GEP) activity, and the PH domain interacts with Phospholipids and is responsible for association of PSCDs with membranes. Members of this family appear to mediate the regulation of protein sorting and membrane trafficking. This encoded protein is involved in the control of Golgi structure and function, and it may have a physiological role in regulating ADP-ribosylation factor protein 6 (ARF) functions, in addition to acting on ARF1. [provided by RefSeq, Jul 2008]

CYTH3 基因产物(4)

mRNA Protein Name
NM_001367580.1 NP_001354509.1 cytohesin-3 isoform b
NM_001367581.1 NP_001354510.1 cytohesin-3 isoform c
NM_001367582.1 NP_001354511.1 cytohesin-3 isoform c
NM_004227.4 NP_004218.1 cytohesin-3 isoform a
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 guanyl-nucleotide exchange factor activity IDA
IDA: 通过直接分析推断
9707577 GOA
enables phosphatidylinositol-3,4,5-trisphosphate binding IDA
IDA: 通过直接分析推断
9742223 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16189514 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in Golgi vesicle transport IMP
IMP: 通过突变表型推断
9707577 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytosol IDA
IDA: 通过直接分析推断
9742223 GOA
located in plasma membrane IDA
IDA: 通过直接分析推断
17398095 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

CYTH3 蛋白结构

Sec7

Sec7: Sec7 domain (66 - 163)

PH

PH: PH domain (182 - 295)

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

cytohesin-3

ARF nucleotide-binding site opener 3

CYTH3 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 CYTH3 O43739 CCDC120 Homo sapiens Q96HB5-4
Validated Y2H
25416956
Intra CYTH3 O43739 CCDC120 Homo sapiens Q96HB5-4
Y2H Prey Pooling
25416956
Intra CYTH3 O43739 SYCE1 Homo sapiens Q8N0S2
Validated Y2H
25416956
Intra CYTH3 O43739 CNKSR1 Homo sapiens Q969H4
Validated Y2H
25416956
Intra CYTH3 O43739 CNKSR1 Homo sapiens Q969H4
Y2H Array
25416956
Intra CYTH3 O43739 CNKSR1 Homo sapiens Q969H4
Y2H Pooling
16189514
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
Corneal Dystrophy, Posterior Amorphous

Posterior Amorphous Corneal Dystrophy

PACD

Chromosome 12q21.33 Deletion Syndrome

Posterior Amorphous Stromal Dystrophy

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
Felis catus CYTH3 VGNC VGNC:69096
Mus musculus CYTH3 MGD MGI:1335107
Rattus norvegicus CYTH3 RGD RGD:620399
Macaca mulatta CYTH3 VGNC VGNC:71829
Bos taurus CYTH3 VGNC VGNC:58371
Canis familiaris CYTH3 VGNC VGNC:49080