gptkbp:instanceOf
|
gptkb:protein
|
gptkbp:alias
|
gptkb:CI-51kD
|
gptkbp:associatedWith
|
gptkb:Leigh_syndrome
mitochondrial complex I deficiency
progressive encephalopathy
|
gptkbp:component
|
gptkb:Complex_I
|
gptkbp:domain
|
flavin mononucleotide (FMN) binding domain
iron-sulfur binding domain
|
gptkbp:encodes
|
gptkb:NADH_dehydrogenase_[ubiquinone]_flavoprotein_1,_mitochondrial
|
gptkbp:Entrez_Gene_ID
|
4723
|
gptkbp:enzymeCommissionNumber
|
1.6.5.3
|
gptkbp:expressedIn
|
mitochondria
|
gptkbp:function
|
oxidoreductase activity
NADH dehydrogenase (ubiquinone) activity
|
gptkbp:gene
|
gptkb:NDUFV1
|
gptkbp:HGNC_ID
|
HGNC:7700
|
https://www.w3.org/2000/01/rdf-schema#label
|
NDUFV1
|
gptkbp:locatedIn
|
mitochondrial inner membrane
|
gptkbp:locatedOnChromosome
|
gptkb:18p11.31
|
gptkbp:molecularWeight
|
51 kDa
|
gptkbp:mutationAssociatedWith
|
gptkb:mitochondrial_complex_I_deficiency,_nuclear_type_1
|
gptkbp:OMIM
|
161015
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
gptkbp:orthologIn
|
gptkb:Danio_rerio
gptkb:Mus_musculus
gptkb:Rattus_norvegicus
|
gptkbp:PDB
|
5XTD
|
gptkbp:RefSeq
|
gptkb:NM_007103
|
gptkbp:subunit
|
gptkb:NADH:ubiquinone_oxidoreductase
|
gptkbp:UniProtID
|
gptkb:P49821
|
gptkbp:bfsParent
|
gptkb:Mitochondrial_Complex_I_protein
|
gptkbp:bfsLayer
|
6
|