Location via proxy:
[ UP ]
[Report a bug]
[Manage cookies]
No cookies
No scripts
No ads
No referrer
Show this form
Homo sapiens (human): 4706
Help
Entry
4706 CDS
T01001
Symbol
NDUFAB1, ACP, ACP1, FASN2A, SDAP
Name
(RefSeq) NADH:ubiquinone oxidoreductase subunit AB1
KO
K03955
NADH dehydrogenase (ubiquinone) 1 alpha/beta subcomplex 1, acyl-carrier protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa00190
Oxidative phosphorylation
hsa01100
Metabolic pathways
hsa04714
Thermogenesis
hsa04723
Retrograde endocannabinoid signaling
hsa04932
Non-alcoholic fatty liver disease
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05208
Chemical carcinogenesis - reactive oxygen species
hsa05415
Diabetic cardiomyopathy
Module
hsa_M00146
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex
hsa_M00873
Fatty acid biosynthesis in mitochondria, animals
Network
nt06460
Alzheimer disease
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
Element
N00995
Electron transfer in Complex I
N00997
Mutation-caused aberrant Abeta to electron transfer in Complex I
N01042
Mutation-caused aberrant SNCA to electron transfer in Complex I
N01043
Mutation-inactivated PINK1 to electron transfer in Complex I
N01044
MPP+ to electron transfer in Complex I
N01045
Rotenone to electron transfer in Complex I
N01136
Mutation-caused aberrant TDP43 to electron transfer in Complex I
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
4706 (NDUFAB1)
09103 Lipid metabolism
00061 Fatty acid biosynthesis
4706 (NDUFAB1)
09150 Organismal Systems
09156 Nervous system
04723 Retrograde endocannabinoid signaling
4706 (NDUFAB1)
09159 Environmental adaptation
04714 Thermogenesis
4706 (NDUFAB1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
4706 (NDUFAB1)
09164 Neurodegenerative disease
05010 Alzheimer disease
4706 (NDUFAB1)
05012 Parkinson disease
4706 (NDUFAB1)
05014 Amyotrophic lateral sclerosis
4706 (NDUFAB1)
05016 Huntington disease
4706 (NDUFAB1)
05020 Prion disease
4706 (NDUFAB1)
05022 Pathways of neurodegeneration - multiple diseases
4706 (NDUFAB1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
4706 (NDUFAB1)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
4706 (NDUFAB1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PP-binding
PP-binding_2
MinE
Motif
Other DBs
NCBI-GeneID:
4706
NCBI-ProteinID:
NP_004994
OMIM:
603836
HGNC:
7694
Ensembl:
ENSG00000004779
Pharos:
O14561
(Tclin)
UniProt:
O14561
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:complement(23581014..23596316)
Genome browser
AA seq
156 aa
AA seq
DB search
MASRVLSAYVSRLPAAFAPLPRVRMLAVARPLSTALCSAGTQTRLGTLQPALVLAQVPGR
VTQLCRQYSDMPPLTLEGIQDRVLYVLKLYDKIDPEKLSVNSHFMKDLGLDSLDQVEIIM
AMEDEFGFEIPDIDAEKLMCPQEIVDYIADKKDVYE
NT seq
471 nt
NT seq
+upstream
nt +downstream
nt
atggcgtctcgtgtcctttcagcctatgtcagccgcctgcccgcggcctttgcgccgctg
ccccgggtccggatgctggccgtggcccggcctctcagcaccgctctctgctccgcgggg
acccagacgaggctcgggactttgcagccggccttagtgctcgcgcaggttcctggtaga
gttacacagttgtgccgccagtatagcgacatgcctcctttgacgttagagggcatccag
gaccgtgttctttacgtattgaaactctatgacaagattgacccagagaagctttcagta
aattctcattttatgaaagacctgggcttagacagtttggaccaagtggagattatcatg
gccatggaagacgaatttgggtttgaaattcctgatatagatgctgaaaagttaatgtgt
ccacaagaaattgtagattacattgcagataagaaggatgtatatgaataa
DBGET
integrated database retrieval system