KEGG   Mustela putorius furo (domestic ferret): 101694292
Entry
101694292         CDS       T07239                                 
Symbol
SDHD
Name
(RefSeq) succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial
  KO
K00237  succinate dehydrogenase (ubiquinone) membrane anchor subunit
Organism
mpuf  Mustela putorius furo (domestic ferret)
Pathway
mpuf00020  Citrate cycle (TCA cycle)
mpuf00190  Oxidative phosphorylation
mpuf01100  Metabolic pathways
mpuf01200  Carbon metabolism
mpuf04714  Thermogenesis
mpuf04932  Non-alcoholic fatty liver disease
mpuf05010  Alzheimer disease
mpuf05012  Parkinson disease
mpuf05014  Amyotrophic lateral sclerosis
mpuf05016  Huntington disease
mpuf05020  Prion disease
mpuf05022  Pathways of neurodegeneration - multiple diseases
mpuf05208  Chemical carcinogenesis - reactive oxygen species
mpuf05415  Diabetic cardiomyopathy
Module
mpuf_M00009  Citrate cycle (TCA cycle, Krebs cycle)
mpuf_M00011  Citrate cycle, second carbon oxidation, 2-oxoglutarate => oxaloacetate
mpuf_M00148  Succinate dehydrogenase (ubiquinone)
Brite
KEGG Orthology (KO) [BR:mpuf00001]
 09100 Metabolism
  09101 Carbohydrate metabolism
   00020 Citrate cycle (TCA cycle)
    101694292 (SDHD)
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    101694292 (SDHD)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    101694292 (SDHD)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101694292 (SDHD)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101694292 (SDHD)
   05012 Parkinson disease
    101694292 (SDHD)
   05014 Amyotrophic lateral sclerosis
    101694292 (SDHD)
   05016 Huntington disease
    101694292 (SDHD)
   05020 Prion disease
    101694292 (SDHD)
   05022 Pathways of neurodegeneration - multiple diseases
    101694292 (SDHD)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101694292 (SDHD)
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    101694292 (SDHD)
SSDB
Motif
Pfam: CybS
Other DBs
NCBI-GeneID: 101694292
NCBI-ProteinID: XP_004749877
UniProt: A0A8U0SUA5
LinkDB
Position
Unknown
AA seq 159 aa
MASLWRLGVLCGAQGGRALFVRIPVVRPVQVSAFLQDQPAPGWCRTQHIHLSPNHYSGSK
AASLHWTGERVVSVLLLGLIPAAYLNPGSAMDYSLAAALTLHSHWGLGQVVTDYVRGDAL
QKAVKAGVLALSALTFAGLCYFNYHDVGICKAVAMLWKL
NT seq 480 nt   +upstreamnt  +downstreamnt
atggcgagtctctggaggctgggtgtcctgtgcggtgcccaaggaggccgagctctgttt
gtccgaattcccgtggtcagacctgttcaggtctcagcatttcttcaggaccagcctgcc
ccaggatggtgtagaacacagcatattcacctgtcacccaaccactattctggttctaag
gctgcatctctccactggactggtgagagggttgtcagtgttttgctcctgggcctaatt
ccagctgcttatttgaatcctggctctgcgatggactactccctggctgcggccctcact
ctccacagtcactggggccttggacaagtggttactgactacgttcgaggggatgctttg
cagaaagctgtcaaagcaggcgttttggcactctcggctctaacctttgctgggctttgt
tatttcaactatcatgacgtgggcatctgcaaagctgttgccatgctgtggaagctctga

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