Electronic Gene Ontology annotations created by ARBA machine learning models

Combined Automated Annotation using Multiple IEA Methods

Identification and characterization of a human mitochondrial NAD kinase.

Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.

Structure of human NADK2 reveals atypical assembly and regulation of NAD kinases from animal mitochondria.

Crystal structure of human NADK2 reveals a dimeric organization and active site occlusion by lysine acetylation.

UniProt record for human NADK2 (Q4G0N4)

UniProt record for donkey NADK2 (A0A8C4M4D0)

NADK2 (donkey): comparison of all donkey NADK2 gene models with human NADK2