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MGI:Bcat2

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Bcat2 ( synonyms: Bcat-2, Eca40 )
Protein Name(s) branched chain aminotransferase 2, mitochondrial,
External Links
MGI MGI:1276534

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0003824

catalytic activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001544
InterPro:IPR018300

F

From MGI

GO:0004084

branched-chain-amino-acid transaminase activity

MGI:MGI:3027291
PMID:14755340[1]

IDA: Inferred from Direct Assay

F

From MGI

GO:0004084

branched-chain-amino-acid transaminase activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:O35854

F

From MGI

GO:0005634

nucleus

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:O35854

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:O35854

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:2682130
PMID:14651853[2]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:3027291
PMID:14755340[1]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:3852644
PMID:18614015[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:O35854

C

From MGI

GO:0006549

isoleucine metabolic process

MGI:MGI:3027291
PMID:14755340[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3028726

P

From MGI

GO:0006550

isoleucine catabolic process

MGI:MGI:3770498
PMID:17767905[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3772355

P

From MGI

GO:0006550

isoleucine catabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:O35854

P

From MGI

GO:0006551

leucine metabolic process

MGI:MGI:3027291
PMID:14755340[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3028726

P

From MGI

GO:0006551

leucine metabolic process

MGI:MGI:3770498
PMID:17767905[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3772355

P

From MGI

GO:0006573

valine metabolic process

MGI:MGI:3027291
PMID:14755340[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3028726

P

From MGI

GO:0006573

valine metabolic process

MGI:MGI:3770498
PMID:17767905[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3772355

P

From MGI

GO:0008483

transaminase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0032

F

From MGI

GO:0008652

cellular amino acid biosynthetic process

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0028

P

From MGI

GO:0009081

branched chain family amino acid metabolic process

MGI:MGI:4442298
PMID:20237068[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3772355

P

From MGI

GO:0009082

branched chain family amino acid biosynthetic process

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0100

P

From MGI

GO:0009083

branched chain family amino acid catabolic process

MGI:MGI:3027291
PMID:14755340[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3028726

P

From MGI

GO:0009083

branched chain family amino acid catabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:O35854

P

From MGI

GO:0009098

leucine biosynthetic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:O35854

P

From MGI

GO:0010817

regulation of hormone levels

MGI:MGI:3770498
PMID:17767905[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3772355

P

From MGI

GO:0016740

transferase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0808

F

From MGI

GO:0052654

L-leucine transaminase activity

MGI:MGI:2152096

IEA: Inferred from Electronic Annotation

EC:2.6.1.42

F

From MGI

GO:0052655

L-valine transaminase activity

MGI:MGI:2152096

IEA: Inferred from Electronic Annotation

EC:2.6.1.42

F

From MGI

GO:0052656

L-isoleucine transaminase activity

MGI:MGI:2152096

IEA: Inferred from Electronic Annotation

EC:2.6.1.42

F

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 1.3 1.4 1.5 Wu JY et al. (2004) ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease. J Clin Invest 113: 434-40 PubMed GONUTS page
  2. Mootha VK et al. (2003) Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria. Cell 115: 629-40 PubMed GONUTS page
  3. Pagliarini DJ et al. (2008) A mitochondrial protein compendium elucidates complex I disease biology. Cell 134: 112-23 PubMed GONUTS page
  4. 4.0 4.1 4.2 4.3 She P et al. (2007) Disruption of BCATm in mice leads to increased energy expenditure associated with the activation of a futile protein turnover cycle. Cell Metab 6: 181-94 PubMed GONUTS page
  5. Lang CH et al. (2010) Alcohol-induced IGF-I resistance is ameliorated in mice deficient for mitochondrial branched-chain aminotransferase. J Nutr 140: 932-8 PubMed GONUTS page
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