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Protein Page:
NUEM (human)
p Phosphorylation
a Acetylation
m Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
u Ubiquitination
s Sumoylation
n Neddylation
gl O-GlcNAc
ga O-GalNAc
h Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage

Overview
NUEM Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Belongs to the complex I NDUFA9 subunit family. Note: This description may include information from UniProtKB.
Protein type: EC 1.6.5.3; Oxidoreductase; Energy Metabolism - oxidative phosphorylation; Mitochondrial; EC 1.6.99.3
Cellular Component: mitochondrial matrix; mitochondrial membrane; mitochondrial inner membrane; mitochondrial respiratory chain complex I
Molecular Function: protein binding; NADH dehydrogenase (ubiquinone) activity; protein complex binding; coenzyme binding; NADH dehydrogenase activity
Biological Process: cellular metabolic process; mitochondrial electron transport, NADH to ubiquinone; sodium ion transport
Reference #:  Q16795 (UniProtKB)
Alt. Names/Synonyms: CI-39kD; Complex I-39kD; MGC111043; NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 9, 39kDa; NADH dehydrogenase (ubiquinone) Fe-S protein 2-like (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial; NADH-ubiquinone oxidoreductase 39 kDa subunit; NDUA9; NDUFA9; NDUFS2L; SDR22E1; short chain dehydrogenase/reductase family 22E, member 1
Gene Symbols: NDUFA9
Molecular weight: 42,510 Da
Basal Isoelectric point: 9.81  Predict pI for various phosphorylation states
Select Structure to View Below

NUEM

Protein Structure Not Found.


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Modification Sites and Domains  
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Modification Sites in Parent Protein, Orthologs, and Isoforms  
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 S78 NHLGRMGsQVIIPYR
0 1 N173 HVSHLNANIKSSSRY
  mouse

 
S78 NHLGRMGSQVIIPYR
S173 HVSHLNAsMKSSSKS
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