NUBPL

Description		nucleotide binding protein like
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Matrix Plasma Membrane
	Molecular Function	Protein Binding ATP Binding Metal Ion Binding 4 Iron, 4 Sulfur Cluster Binding
	Biological Process	Iron-sulfur Cluster Assembly Mitochondrial Respiratory Chain Complex I Assembly Mitochondrion Morphogenesis
Pathways		Complex I biogenesis
Drugs
Diseases		Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome
GWAS		Bitter alcoholic beverage consumption ( 31046077) Brain lesion load ( 19010793) Response to iloperidone treatment (QT prolongation) ( 18521091)
Interacting Genes		3 interacting genes: KDM8 MTUS2 NUBP2
Entrez ID		80224
HPRD ID		16600
Ensembl ID		ENSG00000151413
Uniprot IDs		B3KSK2 B4DWB0 Q8TB37 X5D2R5
PDB IDs
Enriched GO Terms of Interacting Partners?
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