ATE1 - arginyltransferase 1 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 11101

About ATE1

Cytogenetic location: 10q26.13 Genomic coordinates (GRCh38): 10:121,740,424-121,928,463 (from NCBI)

This gene has 73 transcripts (splice variants) and 206 orthologues. Ubiquitous expression in thyroid (RPKM 8.9), testis (RPKM 7.9) and 25 other tissues.

Summary

This gene encodes an arginyltransferase, an enzyme that is involved in posttranslational conjugation of arginine to N-terminal aspartate or glutamate residues. Conjugation of arginine to the N-terminal aspartate or glutamate targets proteins for ubiquitin-dependent degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

ATE1 Products (5)

mRNA Protein Name
NM_001001976.3 NP_001001976.1 arginyl-tRNA--protein transferase 1 isoform 1
NM_001288734.2 NP_001275663.1 arginyl-tRNA--protein transferase 1 isoform 3
NM_001288735.2 NP_001275664.1 arginyl-tRNA--protein transferase 1 isoform 4
NM_001288736.2 NP_001275665.1 arginyl-tRNA--protein transferase 1 isoform 5
NM_007041.4 NP_008972.2 arginyl-tRNA--protein transferase 1 isoform 2
Molecular Function GO Annotation Evidence References Source
enables arginyl-tRNA--protein transferase activity IDA
IDA: Inferred from direct assay
34893540 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
23455924 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within proteasomal protein catabolic process IMP
IMP: Inferred from mutant phenotype
25970626 GOA
involved in response to oxidative stress IDA
IDA: Inferred from direct assay
34893540 GOA
involved in ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
34893540 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
9858543 GOA
located in nucleus IDA
IDA: Inferred from direct assay
9858543 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ATE1 Protein Structure

ATE_N

ATE_N: Arginine-tRNA-protein transferase, N terminus (18 - 92)

ATE_C

ATE_C: Arginine-tRNA-protein transferase, C terminus (290 - 432)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 518 a.a.
Protein Preferred Names Protein Names

arginyl-tRNA--protein transferase 1

  • R-transferase 1

ATE1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ATE1 O95260 SUV39H1 Homo sapiens O43463 23455924
Cross: Cross-species interaction Intra: Intraspecies interaction

ATE1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82433 ATE1 Antibody (YA2178) WB, IHC-P Human, Rat
HY-P82433A ATE1 Antibody (YA2178)(PBS only) WB, IHC-P Human, Rat

Related Diseases

Diseases Alias
Johanson-Blizzard Syndrome
  • JBS

  • Nasal Alar Hypoplasia, Hypothyroidism, Pancreatic Achylia, And Congenital Deafness

  • Nasal Alar Hypoplasia, Hypothyroidism, Pancreatic Achylia And Congenital Deafness

  • Johanson Blizzard Syndrome

Chromosome 10q26 Deletion Syndrome
  • Distal 10q Deletion Syndrome

  • Terminal Chromosome 10q26 Deletion Syndrome

  • Distal Monosomy 10q

  • Monosomy 10qter

  • Telomeric Deletion 10q

  • Distal Deletion 10q

  • 10q26 Deletion Syndrome

  • 10qter Deletion

  • Telomeric Deletion 10

Beare-Stevenson Cutis Gyrata Syndrome
  • Cutis Gyrata Syndrome Of Beare And Stevenson

  • Beare-Stevenson Syndrome

  • BSTVS

  • Cutis Gyrata-Acanthosis Nigricans-Craniosynostosis Syndrome

  • Beare Stevenson Syndrome

  • Cutis Gyrata - Acanthosis Nigricans - Craniosynostosis

  • Cutis Gyrata Syndrome Of Beare-Stevenson

Jackson-Weiss Syndrome
  • JWS

  • Craniosynostosis, Midfacial Hypoplasia, And Foot Abnormalities

  • Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities Syndrome

  • Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities

Diseases Alias
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

Orthologs Information

Species Symbol Source ID
Mus musculus ATE1 MGD MGI:1333870
Rattus norvegicus ATE1 RGD RGD:1309335
Macaca mulatta ATE1 VGNC VGNC:70168
Bos taurus ATE1 VGNC VGNC:26238
Felis catus ATE1 VGNC VGNC:68493
Canis familiaris ATE1 VGNC VGNC:38206
Others ATE1 NCBI