1. Gene
  2. MOCS3 - molybdenum cofactor synthesis 3 Gene

MOCS3 - molybdenum cofactor synthesis 3 Gene

中文名称:钼辅助因子合成 3

种属: Homo sapiens

同用名: UBA4

基因 ID: 27304 | 基因类型: protein coding

关于 MOCS3

Cytogenetic location: 20q13.13 Genomic coordinates (GRCh38): 20:50,958,818-50,963,929 (from NCBI)

This gene has 1 transcript (splice variant), 195 orthologues and 9 paralogues.

功能概要

钼辅助因子 (MoCo) 是所有钼酶发挥功能所必需的。由该基因编码的蛋白质腺苷酸化并激活钼蝶呤合酶,这是一种生物合成 MoCo 所需的酶。该基因不含内含子。该基因的假基因存在于 14 号染色体上。[RefSeq 提供,2012 年 11 月]

Molybdenum cofactor (MoCo) is necessary for the function of all molybdoenzymes. The protein encoded by this gene adenylates and activates molybdopterin synthase, an Enzyme required for biosynthesis of MoCo. This gene contains no introns. A pseudogene of this gene is present on chromosome 14. [provided by RefSeq, Nov 2012]

MOCS3 基因产物(1)

mRNA Protein Name
NM_014484.5 NP_055299.1 adenylyltransferase and sulfurtransferase MOCS3
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 URM1 activating enzyme activity IDA
IDA: 通过直接分析推断
19017811 GOA
enables molybdopterin-synthase sulfurtransferase activity IDA
IDA: 通过直接分析推断
15073332 GOA
enables molybdopterin-synthase sulfurtransferase activity IMP
IMP: 通过突变表型推断
15073332 GOA
enables nucleotidyltransferase activity IDA
IDA: 通过直接分析推断
19017811 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
18650437 GOA
enables sulfurtransferase activity IDA
IDA: 通过直接分析推断
15910006 GOA
enables sulfurtransferase activity IMP
IMP: 通过突变表型推断
17459099 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in Mo-molybdopterin cofactor biosynthetic process IDA
IDA: 通过直接分析推断
15073332 GOA
involved in Mo-molybdopterin cofactor biosynthetic process IMP
IMP: 通过突变表型推断
30817134 GOA
involved in molybdopterin cofactor metabolic process IDA
IDA: 通过直接分析推断
18650437 GOA
involved in tRNA thio-modification IDA
IDA: 通过直接分析推断
19017811 GOA
involved in tRNA thio-modification IMP
IMP: 通过突变表型推断
30817134 GOA
involved in tRNA wobble uridine modification IDA
IDA: 通过直接分析推断
19017811 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
23593335 GOA
located in cytosol IDA
IDA: 通过直接分析推断
15073332 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

MOCS3 蛋白结构

ThiF

ThiF: ThiF family (85 - 213)

(219 - 303)

Rhodanese

Rhodanese: Rhodanese-like domain (351 - 451)

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

adenylyltransferase and sulfurtransferase MOCS3

MPT synthase sulfurylase

MOCS3 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
MOCS3 O95396 TARDBP Homo sapiens Q13148
Validated Y2H
32814053
种属内
MOCS3 O95396 TARDBP Homo sapiens Q13148
Y2H Array
32814053
种属内
MOCS3 O95396 TARDBP Homo sapiens Q13148
Y2H Pooling
32814053
种属内
MOCS3 O95396 ATXN1 Homo sapiens P54253
Y2H Pooling
32814053
种属内
MOCS3 O95396 ATXN1 Homo sapiens P54253
Validated Y2H
32814053
种属内
MOCS3 O95396 ATXN1 Homo sapiens P54253
Y2H Array
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
Molybdenum Cofactor Deficiency

Combined Molybdoflavoprotein Enzyme Deficiency

Mocod

Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase, And Aldehyde Oxidase

Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase And Aldehyde Oxidase

Combined Xanthine Oxidase And Sulfite Oxidase And Aldehyde Oxidase Deficiency

Deficiency Of Molybdenum Cofactor

Deficiency, Molybdenum Cofactor

Molybdenum Cofactor Deficiency, Complementation Group C

MOCODC

Sulfite Oxidase Deficiency Due To Molybdenum Cofactor Deficiency Type C

Molybdenum Cofactor Deficiency C

Molybdenum Cofactor Deficiency Type C

Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase And Aldehyde Oxidase Type C

Mocod Type C

Molybdenum Cofactor Deficiency Complementation Group C

Deficiency, Molybdenum Cofactor, Complementation Group C

Sulfite Oxidase Deficiency, Isolated

Sulfite Oxidase Deficiency

Sulfocysteinuria

Isolated Sulfite Oxidase Deficiency

ISOD

Encephalopathy Due To Sulfite Oxidase Deficiency

Molybdenum Cofactor Deficiency, Complementation Group A

MOCODA

Sulfite Oxidase Deficiency Due To Molybdenum Cofactor Deficiency Type A

Molybdenum Cofactor Deficiency A

Molybdenum Cofactor Deficiency Type A

Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase And Aldehyde Oxidase Type A

Mocod Type A

Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase, And Aldehyde Oxidase

Sulfite Oxidase, Xanthine Dehydrogenase, And Aldehyde Oxidase, Combined Deficiency Of

Molybdenum Cofactor Deficiency Complementation Group A

Molybdenum Cofactor Deficiency, Type A

Deficiency, Molybdenum Cofactor, Complementation Group A

Molybdenum Cofactor Deficiency, Complementation Group B

MOCODB

Sulfite Oxidase Deficiency Due To Molybdenum Cofactor Deficiency Type B

Molybdenum Cofactor Deficiency B

Molybdenum Cofactor Deficiency Type B

Combined Deficiency Of Sulfite Oxidase, Xanthine Dehydrogenase And Aldehyde Oxidase Type B

Mocod Type B

Molybdenum Cofactor Deficiency Complementation Group B

Deficiency, Molybdenum Cofactor, Complementation Group B

Neu-Laxova Syndrome 2

NLS2

Encephalomalacia
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
Canis familiaris MOCS3 VGNC VGNC:43307
Bos taurus MOCS3 VGNC VGNC:31549
Macaca mulatta MOCS3 VGNC VGNC:74772
Rattus norvegicus MOCS3 RGD RGD:1307044
Mus musculus MOCS3 MGD MGI:1916622
Felis catus MOCS3 VGNC VGNC:63550