KEGG   Rhinolophus ferrumequinum (greater horseshoe bat): 117026373
Entry
117026373         CDS       T07722                                 
Name
(RefSeq) cytochrome c-like
  KO
K08738  cytochrome c
Organism
rfq  Rhinolophus ferrumequinum (greater horseshoe bat)
Pathway
rfq00190  Oxidative phosphorylation
rfq01100  Metabolic pathways
rfq01524  Platinum drug resistance
rfq04115  p53 signaling pathway
rfq04210  Apoptosis
rfq04215  Apoptosis - multiple species
rfq04932  Non-alcoholic fatty liver disease
rfq05010  Alzheimer disease
rfq05012  Parkinson disease
rfq05014  Amyotrophic lateral sclerosis
rfq05016  Huntington disease
rfq05017  Spinocerebellar ataxia
rfq05020  Prion disease
rfq05022  Pathways of neurodegeneration - multiple diseases
rfq05132  Salmonella infection
rfq05134  Legionellosis
rfq05145  Toxoplasmosis
rfq05152  Tuberculosis
rfq05160  Hepatitis C
rfq05161  Hepatitis B
rfq05162  Measles
rfq05163  Human cytomegalovirus infection
rfq05164  Influenza A
rfq05167  Kaposi sarcoma-associated herpesvirus infection
rfq05168  Herpes simplex virus 1 infection
rfq05169  Epstein-Barr virus infection
rfq05170  Human immunodeficiency virus 1 infection
rfq05200  Pathways in cancer
rfq05210  Colorectal cancer
rfq05222  Small cell lung cancer
rfq05416  Viral myocarditis
rfq05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:rfq00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    117026373
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    117026373
   04215 Apoptosis - multiple species
    117026373
   04115 p53 signaling pathway
    117026373
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    117026373
  09162 Cancer: specific types
   05210 Colorectal cancer
    117026373
   05222 Small cell lung cancer
    117026373
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    117026373
   05161 Hepatitis B
    117026373
   05160 Hepatitis C
    117026373
   05164 Influenza A
    117026373
   05162 Measles
    117026373
   05168 Herpes simplex virus 1 infection
    117026373
   05163 Human cytomegalovirus infection
    117026373
   05167 Kaposi sarcoma-associated herpesvirus infection
    117026373
   05169 Epstein-Barr virus infection
    117026373
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    117026373
   05134 Legionellosis
    117026373
   05152 Tuberculosis
    117026373
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    117026373
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117026373
   05012 Parkinson disease
    117026373
   05014 Amyotrophic lateral sclerosis
    117026373
   05016 Huntington disease
    117026373
   05017 Spinocerebellar ataxia
    117026373
   05020 Prion disease
    117026373
   05022 Pathways of neurodegeneration - multiple diseases
    117026373
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    117026373
   05416 Viral myocarditis
    117026373
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    117026373
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    117026373
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG
Other DBs
NCBI-GeneID: 117026373
NCBI-ProteinID: XP_032969023
Ensembl: ENSRFEG00010004537
LinkDB
Position
X:complement(54856808..54857218)
AA seq 105 aa
MGDVEKGKKIFVQKCAQCHTVEKAGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKTAERADLIAYLKKATKE
NT seq 318 nt   +upstreamnt  +downstreamnt
atgggtgatgttgagaagggcaagaagatttttgtgcagaagtgtgcccagtgccatact
gtggaaaaggcaggcaagcacaagactgggccaaatctccatggtctgtttgggcgaaag
actggtcaggcccctggattttcttacacggatgccaacaagaacaaaggtatcacctgg
ggagaagaaaccttgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagactgcagaaagggcagacttgatagcgtatctcaaa
aaggctactaaggaataa

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