{ "uniprot_canonical_ac": "A2AIL4-1", "ptm_annotation": [], "sequence": { "header": "sp|A2AIL4-1|NDUF6_MOUSE Isoform 1 of NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 OS=Mus musculus OX=10090 GN=Ndufaf6 PE=1 SV=1 CANONICAL=A2AIL4-1", "length": 333, "sequence": "MATSMLGSVRGPRPFGLANLFHRQPPRDAWERVRRLPGPSAVRRSVAAASGPGIPGSHLYCLELLRKRDYESYLCSLLFPAECQRSASALRAFNVELAQVKDSVSEKTIGLMRMQFWKKAVEDMYCDNPPHQPVAIELWKAVKKHNLTKRWLMRIIDEREKNLDDKAYRSMQELENYAENTQGSLLYLTLEVLGVKDLHADHAASHIGKAQGIVTCLRATPYHSSRRQVFLPMDVCVQHGVSQEDFLRRNQDKNVRDVVYDIASQAHLHLKHARSFHRSVPAEAFPAFLQTVSLEDYLKKIQRVDFDIFHPSLQQKNMLLPLSLYIQSWRKRY" }, "uniprot_id": "", "glycation": [], "keywords": [], "species": [ { "common_name": "Mouse", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" } ], "name": "Mus musculus", "taxid": 10090 } ], "reaction_enzymes": [], "publication": [ { "reference": [ { "url": "https://www.ncbi.nlm.nih.gov/pubmed/18614015", "type": "PubMed", "id": "18614015" } ], "title": "A mitochondrial protein compendium elucidates complex I disease biology.", "journal": "Cell", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" } ], "authors": "Calvo S.E., Mootha V.K., Pagliarini D.J., Thorburn D.R., Vidal M., Carr S.A., Hill D.E., Chang B., Boneh A., Ong S.E., Sheth S.A., Chen W.K., Evans J.G., Sugiana C., Vafai S.B., Walford G.A.", "date": "2008" }, { "reference": [ { "url": "https://www.ncbi.nlm.nih.gov/pubmed/31097699", "type": "PubMed", "id": "31097699" } ], "title": "Yin Yang 1 sustains biosynthetic demands during brain development in a stage-specific manner.", "journal": "Nature communications", "evidence": [ { "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001078962.1", "id": "NP_001078962.1", "database": "RefSeq" } ], "authors": "Zurkirchen L, Varum S, Giger S, Klug A, Hausel J, Bossart R, Zemke M, Cantu C, Atak ZK, Zamboni N, Basler K, Sommer L", "date": "2019" } ], "uniprot_ac": "A2AIL4", "gene_names": [ { "url": "https://www.ncbi.nlm.nih.gov/protein/A2AIL4", "type": "synonym", "resource": "RefSeq", "name": "2310030N02Rik" }, { "url": "https://www.ncbi.nlm.nih.gov/protein/A2AIL4", "type": "synonym", "resource": "RefSeq", "name": "Ndufaf6" }, { "url": "https://www.uniprot.org/uniprot/A2AIL4", "type": "recommended", "resource": "UniProtKB", "name": "Ndufaf6" } ], "reactions": [], "isoforms": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4#A2AIL4-1", "isoform_ac": "A2AIL4-1", "locus": { "end_pos": 11051100, "strand": "+", "start_pos": 11076176, "chromosome": "4", "evidence": [ { "url": "https://www.ensembl.org/id/ENSMUST00000058183", "id": "ENSMUST00000058183", "database": "Ensembl Transcript" }, { "url": "https://www.ensembl.org/id/ENSMUSP00000062039", "id": "ENSMUSP00000062039", "database": "Ensembl Peptide" } ] }, "sequence": { "header": "sp|A2AIL4-1|NDUF6_MOUSE Isoform 1 of NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 OS=Mus musculus OX=10090 GN=Ndufaf6 PE=1 SV=1 CANONICAL=A2AIL4-1", "length": 333, "sequence": "MATSMLGSVRGPRPFGLANLFHRQPPRDAWERVRRLPGPSAVRRSVAAASGPGIPGSHLYCLELLRKRDYESYLCSLLFPAECQRSASALRAFNVELAQVKDSVSEKTIGLMRMQFWKKAVEDMYCDNPPHQPVAIELWKAVKKHNLTKRWLMRIIDEREKNLDDKAYRSMQELENYAENTQGSLLYLTLEVLGVKDLHADHAASHIGKAQGIVTCLRATPYHSSRRQVFLPMDVCVQHGVSQEDFLRRNQDKNVRDVVYDIASQAHLHLKHARSFHRSVPAEAFPAFLQTVSLEDYLKKIQRVDFDIFHPSLQQKNMLLPLSLYIQSWRKRY" } } ], "pathway": [ { "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:76947", "resource": "KEGG Pathway", "id": "mmu:76947", "name": "" }, { "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-6799198", "description": "Complex I biogenesis", "resource": "Reactome", "id": "R-MMU-6799198", "name": "Complex I biogenesis" } ], "reaction_participants": [], "function": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4#function", "annotation": "Involved in the assembly of mitochondrial NADH:ubiquinone oxidoreductase complex (complex I) at early stages. May play a role in the biogenesis of MT-ND1 (By similarity).", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4#function", "id": "A2AIL4", "database": "UniProtKB" } ] } ], "orthologs": [ { "uniprot_canonical_ac": "D3ZN43-1", "protein_name": "NADH dehydrogenase (ubiquinone) complex I, assembly factor 6", "sequence": { "length": 333, "sequence": "MATSMLGSVPGPRPFGLAGLFRRRPPRDPWERVRRLPRLSAVRRSVAAASGPGIPDSHLYCLELLRKRDYESYLCSLLFPAECQRSASALRAFNVELAQVKDSVSEKTIGLMRMQFWRKAVEDMFCDNPPHQPVAMELWKAVKRHNLTKRWLLRIIDEREKNLDDKAYRSIRELETYAENTQSSLLYLTLEVLGVKDVHADHAASHIGKAQGIVTCLRATPYHSSRRQVFLPMDVCVQHGVSQEDFLRRNQDKNVRDVVYDIASQAHLHLKHARSFHSRVPAEAFPAFLQTVSLEDYLKKIQRVDFDIFHPSLQQKNTLLPLSLYIQSWRKRY" }, "evidence": [ { "url": "http://www.informatics.jax.org/homology/43831", "id": "43831", "database": "MGI" } ], "common_name": "Rat", "organism": "Rattus norvegicus", "gene_name": "Ndufaf6", "tax_id": 10116 }, { "uniprot_canonical_ac": "Q330K2-1", "protein_name": "NADH dehydrogenase (ubiquinone) complex I, assembly factor 6", "sequence": { "length": 333, "sequence": "MAASAHGSVWGPLRLGIPGLCCRRPPLGLYARMRRLPGPEVSGRSVAAASGPGAWGTDHYCLELLRKRDYEGYLCSLLLPAESRSSVFALRAFNVELAQVKDSVSEKTIGLMRMQFWKKTVEDIYCDNPPHQPVAIELWKAVKRHNLTKRWLMKIVDEREKNLDDKAYRNIKELENYAENTQSSLLYLTLEILGIKDLHADHAASHIGKAQGIVTCLRATPYHGSRRKVFLPMDICMLHGVSQEDFLRRNQDKNVRDVIYDIASQAHLHLKHARSFHKTVPVKAFPAFLQTVSLEDFLKKIQRVDFDIFHPSLQQKNTLLPLYLYIQSWRKTY" }, "evidence": [ { "url": "http://www.informatics.jax.org/homology/43831", "id": "43831", "database": "MGI" }, { "url": "https://omabrowser.org/oma/group/A2AIL4/", "id": "A2AIL4", "database": "OMA" } ], "common_name": "Human", "organism": "Homo sapiens", "gene_name": "NDUFAF6", "tax_id": 9606 } ], "interactions": [], "synthesized_glycans": [], "snv": [], "cluster_types": [ { "name": "homologset.mgi", "label": "MGI Homologs" }, { "name": "homologset.oma", "label": "OMA Homologs" } ], "refseq": { "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001078962.1", "ac": "NP_001078962.1", "name": "NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 precursor", "summary": "" }, "go_annotation": { "categories": [ { "go_terms": [ { "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739", "pmid": "18614015", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" } ], "name": "mitochondrion", "id": "GO:0005739" }, { "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634", "pmid": "", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" } ], "name": "nucleus", "id": "GO:0005634" }, { "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737", "pmid": "", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" } ], "name": "cytoplasm", "id": "GO:0005737" }, { "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005743", "pmid": "", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" } ], "name": "mitochondrial inner membrane", "id": "GO:0005743" } ], "total": 4, "name": "Cellular Component" }, { "go_terms": [ { "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032981", "pmid": "", "evidence": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" } ], "name": "mitochondrial respiratory chain complex I assembly", "id": "GO:0032981" } ], "total": 1, "name": "Biological Process" } ] }, "site_annotation": [ { "end_pos": 148, "annotation": "n_glycosylation_sequon", "start_pos": 146 } ], "pro_annotation": [], "crossref": [ { "url": "https://bgee.org/?page=gene&gene_id=ENSMUSG00000050323", "id": "ENSMUSG00000050323", "database": "Bgee" }, { "url": "https://www.ncbi.nlm.nih.gov/gene/76947", "id": "76947", "database": "GeneID" }, { "url": "https://www.ebi.ac.uk/interpro/entry/IPR008949", "id": "IPR008949", "database": "InterPro" }, { "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:76947", "id": "mmu:76947", "database": "KEGG Pathway" }, { "url": "http://www.informatics.jax.org/marker/MGI:1924197", "id": "1924197", "database": "MGI" }, { "url": "https://omabrowser.org/oma/group/KIQQVDF/", "id": "KIQQVDF", "database": "OMA" }, { "url": "http://www.orthodb.org/?query=616989at2759", "id": "616989at2759", "database": "OrthoDB" }, { "url": "http://purl.obolibrary.org/obo/PR_PR_A2AIL4", "id": "PR_A2AIL4", "database": "PRO" }, { "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-6799198", "id": "R-MMU-6799198", "database": "Reactome" }, { "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001078962", "id": "NP_001078962", "database": "RefSeq" }, { "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001078962.1", "id": "NP_001078962.1", "database": "RefSeq" }, { "url": "https://www.uniprot.org/uniprot/A2AIL4", "id": "A2AIL4", "database": "UniProtKB" }, { "url": "https://www.uniprot.org/uniprot/A2AIL4-1", "id": "A2AIL4-1", "database": "UniProtKB" } ], "expression_disease": [], "glycosylation": [], "mutagenesis": [], "disease": [ { "disease_id": "DOID:0060536", "synonyms": [ { "url": "http://disease-ontology.org/term/DOID:0060536", "resource": "Disease Ontology", "description": "", "name": "isolated mitochondrial respiratory chain complex I deficiency", "id": "DOID:0060536" }, { "url": "http://disease-ontology.org/term/DOID:0060536", "resource": "Disease Ontology", "description": "", "name": "isolated NADH-coenzyme Q reductase deficiency", "id": "DOID:0060536" }, { "url": "http://disease-ontology.org/term/DOID:0060536", "resource": "Disease Ontology", "description": "", "name": "isolated NADH-CoQ reductase deficiency", "id": "DOID:0060536" }, { "url": "http://disease-ontology.org/term/DOID:0060536", "resource": "Disease Ontology", "description": "", "name": "isolated NADH-ubiquinone reductase deficiency", "id": "DOID:0060536" } ], "recommended_name": { "url": "http://disease-ontology.org/term/DOID:0060536", "resource": "Disease Ontology", "description": "A mitochondrial metabolism disease characterized by a wide range of manifestations including marked and often fatal lactic acidosis, cardiomyopathy, leukoencephalopathy, pure myopathy and hepatopathy with tubulopathy. Among the numerous clinical phenotypes observed are Leigh syndrome, Leber hereditary optic neuropathy and MELAS syndrome. It can have material basis in mutations in multiple different genes, both nuclear-encoded and mitochondrial-encoded.", "name": "mitochondrial complex I deficiency", "id": "DOID:0060536" }, "evidence": [ { "url": "https://www.alliancegenome.org/gene/0060536#disease-associations", "id": "0060536", "database": "Alliance of Genome Resources" } ] }, { "disease_id": "DOID:0080761", "synonyms": [ { "url": "http://disease-ontology.org/term/DOID:0080761", "resource": "Disease Ontology", "description": "", "name": "Acadian-variant Fanconi syndrome", "id": "DOID:0080761" } ], "recommended_name": { "url": "http://disease-ontology.org/term/DOID:0080761", "resource": "Disease Ontology", "description": "A Fanconi syndrome that is characterized by proximal renotubular dysfunction from birth, followed by progressive kidney disease and pulmonary fibrosis and that has_material_basis_in homozygous mutation in the NDUFAF6 gene on chromosome 8q22.", "name": "Fanconi renotubular syndrome 5", "id": "DOID:0080761" }, "evidence": [ { "url": "https://www.alliancegenome.org/gene/0080761#disease-associations", "id": "0080761", "database": "Alliance of Genome Resources" } ] }, { "disease_id": "DOID:3652", "synonyms": [ { "url": "http://disease-ontology.org/term/DOID:3652", "resource": "Disease Ontology", "description": "", "name": "Infantile necrotizing encephalomyelopathy", "id": "DOID:3652" }, { "url": "http://disease-ontology.org/term/DOID:3652", "resource": "Disease Ontology", "description": "", "name": "juvenile subacute necrotizing encephalomyelopathy", "id": "DOID:3652" }, { "url": "http://disease-ontology.org/term/DOID:3652", "resource": "Disease Ontology", "description": "", "name": "Leigh syndrome", "id": "DOID:3652" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome due to mitochondrial Complex 1 deficiency", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome due to mitochondrial Complex 3 deficiency", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome; LS", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "necrotizing encephalopathy, infantile Subacute, of Leigh", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "LS", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome due to mitochondrial Complex 4 deficiency", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome due to mitochondrial Complex 5 deficiency", "id": "MONDO:0009723" }, { "url": "https://monarchinitiative.org/disease/MONDO:0009723", "resource": "MONDO", "description": "", "name": "Leigh syndrome due to mitochondrial Complex 2 deficiency", "id": "MONDO:0009723" }, { "url": "https://www.omim.org/entry/256000", "resource": "MIM", "description": "Leigh syndrome", "name": "Leigh syndrome", "id": "MIM:256000" } ], "recommended_name": { "url": "http://disease-ontology.org/term/DOID:3652", "resource": "Disease Ontology", "description": "A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.", "name": "Leigh disease", "id": "DOID:3652" }, "evidence": [ { "url": "https://www.alliancegenome.org/gene/3652#disease-associations", "id": "3652", "database": "Alliance of Genome Resources" } ] }, { "disease_id": "DOID:8466", "synonyms": [ { "url": "http://disease-ontology.org/term/DOID:8466", "resource": "Disease Ontology", "description": "", "name": "degeneration of retina", "id": "DOID:8466" } ], "recommended_name": { "url": "http://disease-ontology.org/term/DOID:8466", "resource": "Disease Ontology", "description": "A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina.", "name": "retinal degeneration", "id": "DOID:8466" }, "evidence": [ { "url": "https://www.alliancegenome.org/gene/8466#disease-associations", "id": "8466", "database": "Alliance of Genome Resources" } ] } ], "phosphorylation": [], "mass": { "monoisotopic_mass": 38362.0, "chemical_mass": 38362.0 }, "expression_tissue": [], "gene": [ { "url": "https://www.uniprot.org/uniprot/A2AIL4", "name": "Ndufaf6", "locus": { "end_pos": 11051045, "strand": "-", "start_pos": 11076205, "chromosome": "4", "evidence": [ { "url": "https://www.ensembl.org/id/ENSMUSG00000050323", "id": "ENSMUSG00000050323", "database": "Ensembl Gene" } ] } } ], "protein_names": [ { "url": "https://www.ncbi.nlm.nih.gov/protein/A2AIL4", "type": "synonym", "resource": "RefSeq", "name": "NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 precursor" }, { "url": "https://www.uniprot.org/uniprot/A2AIL4#names_and_taxonomy", "type": "recommended", "resource": "UniProtKB", "name": "NADH dehydrogenase (ubiquinone) complex I, assembly factor 6" }, { "url": "https://www.ncbi.nlm.nih.gov/protein/A2AIL4", "type": "synonym", "resource": "RefSeq", "name": "UPF0551 protein C8orf38 homolog, mitochondrial; NADH dehydrogenase (ubiquinone) complex I, assembly factor 6" } ] }