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MGI:Agtpbp1

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Agtpbp1 ( synonyms: Nna1 )
Protein Name(s) ATP/GTP binding protein 1,
External Links
MGI MGI:2159437

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001754

eye photoreceptor cell differentiation

MGI:MGI:3614720
PMID:16465590[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0004180

carboxypeptidase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0121

F

From MGI

GO:0004181

metallocarboxypeptidase activity

MGI:MGI:4849873
PMID:21074048[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005515

protein binding

MGI:MGI:4849873
PMID:21074048[2]

IPI: Inferred from Physical Interaction

UniProtKB:Q6PDN3

F

From MGI

GO:0005634

nucleus

MGI:MGI:2159471
PMID:11083920[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:2159471
PMID:11083920[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:4821195
PMID:20620870[4]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005829

cytosol

MGI:MGI:4887331
PMID:17244818[5]

IDA: Inferred from Direct Assay

C

From MGI

GO:0006508

proteolysis

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0645

P

From MGI

GO:0006508

proteolysis

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000834

P

From MGI

GO:0007005

mitochondrion organization

MGI:MGI:4821195
PMID:20620870[4]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0007628

adult walking behavior

MGI:MGI:3694543
PMID:16952463[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857523

P

From MGI

GO:0008219

cell death

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0523

P

From MGI

GO:0008233

peptidase activity

MGI:MGI:4821195
PMID:20620870[4]

TAS: Traceable Author Statement

F

From MGI

GO:0008237

metallopeptidase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0482

F

From MGI

GO:0008270

zinc ion binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000834

F

From MGI

GO:0015631

tubulin binding

MGI:MGI:4849873
PMID:21074048[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0016787

hydrolase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0378

F

From MGI

GO:0021680

cerebellar Purkinje cell layer development

MGI:MGI:4849309
PMID:21052544[7]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0021702

cerebellar Purkinje cell differentiation

MGI:MGI:1347769
PMID:10630211[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856535

P

From MGI

GO:0021702

cerebellar Purkinje cell differentiation

MGI:MGI:2159417
PMID:11884758[9]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0021702

cerebellar Purkinje cell differentiation

MGI:MGI:3614720
PMID:16465590[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0021702

cerebellar Purkinje cell differentiation

MGI:MGI:4849873
PMID:21074048[2]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0021772

olfactory bulb development

MGI:MGI:2159417
PMID:11884758[9]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0035609

C-terminal protein deglutamylation

MGI:MGI:4849873
PMID:21074048[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0035610

protein side chain deglutamylation

MGI:MGI:4849873
PMID:21074048[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0042133

neurotransmitter metabolic process

MGI:MGI:62875
PMID:8100981[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856535

P

From MGI

GO:0046872

metal ion binding

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0479

F

From MGI

GO:0050905

neuromuscular process

MGI:MGI:1347769
PMID:10630211[8]

IGI: Inferred from Genetic Interaction

MGI:MGI:109482

P

From MGI

GO:0050905

neuromuscular process

MGI:MGI:2159417
PMID:11884758[9]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0060041

retina development in camera-type eye

MGI:MGI:4849309
PMID:21052544[7]

IMP: Inferred from Mutant Phenotype

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 Chakrabarti L et al. (2006) The Purkinje cell degeneration 5J mutation is a single amino acid insertion that destabilizes Nna1 protein. Mamm Genome 17: 103-10 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 2.4 2.5 Rogowski K et al. (2010) A family of protein-deglutamylating enzymes associated with neurodegeneration. Cell 143: 564-78 PubMed GONUTS page
  3. 3.0 3.1 Harris A et al. (2000) Regenerating motor neurons express Nna1, a novel ATP/GTP-binding protein related to zinc carboxypeptidases. Mol Cell Neurosci 16: 578-96 PubMed GONUTS page
  4. 4.0 4.1 4.2 Chakrabarti L et al. (2010) Mitochondrial dysfunction in NnaD mutant flies and Purkinje cell degeneration mice reveals a role for Nna proteins in neuronal bioenergetics. Neuron 66: 835-47 PubMed GONUTS page
  5. Kalinina E et al. (2007) A novel subfamily of mouse cytosolic carboxypeptidases. FASEB J 21: 836-50 PubMed GONUTS page
  6. Wang T et al. (2006) The carboxypeptidase-like substrate-binding site in Nna1 is essential for the rescue of the Purkinje cell degeneration (pcd) phenotype. Mol Cell Neurosci 33: 200-13 PubMed GONUTS page
  7. 7.0 7.1 Won J et al. (2011) Mouse model resources for vision research. J Ophthalmol 2011: 391384 PubMed GONUTS page
  8. 8.0 8.1 Campbell DB et al. (1999) Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background. Exp Neurol 160: 268-78 PubMed GONUTS page
  9. 9.0 9.1 9.2 Fernandez-Gonzalez A et al. (2002) Purkinje cell degeneration (pcd) phenotypes caused by mutations in the axotomy-induced gene, Nna1. Science 295: 1904-6 PubMed GONUTS page
  10. Matsui K et al. (1993) Levels of somatostatin and cholecystokinin in the brain of ataxic mutant mice. Life Sci 53: 333-40 PubMed GONUTS page
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