KEGG   Macaca nemestrina (pig-tailed macaque): 105491771
Entry
105491771         CDS       T08765                                 
Name
(RefSeq) cytochrome c-like
  KO
K08738  cytochrome c
Organism
mni  Macaca nemestrina (pig-tailed macaque)
Pathway
mni00190  Oxidative phosphorylation
mni01100  Metabolic pathways
mni01524  Platinum drug resistance
mni04115  p53 signaling pathway
mni04210  Apoptosis
mni04215  Apoptosis - multiple species
mni04932  Non-alcoholic fatty liver disease
mni05010  Alzheimer disease
mni05012  Parkinson disease
mni05014  Amyotrophic lateral sclerosis
mni05016  Huntington disease
mni05017  Spinocerebellar ataxia
mni05020  Prion disease
mni05022  Pathways of neurodegeneration - multiple diseases
mni05132  Salmonella infection
mni05134  Legionellosis
mni05145  Toxoplasmosis
mni05152  Tuberculosis
mni05160  Hepatitis C
mni05161  Hepatitis B
mni05162  Measles
mni05163  Human cytomegalovirus infection
mni05164  Influenza A
mni05167  Kaposi sarcoma-associated herpesvirus infection
mni05168  Herpes simplex virus 1 infection
mni05169  Epstein-Barr virus infection
mni05170  Human immunodeficiency virus 1 infection
mni05200  Pathways in cancer
mni05210  Colorectal cancer
mni05222  Small cell lung cancer
mni05416  Viral myocarditis
mni05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:mni00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    105491771
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    105491771
   04215 Apoptosis - multiple species
    105491771
   04115 p53 signaling pathway
    105491771
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105491771
  09162 Cancer: specific types
   05210 Colorectal cancer
    105491771
   05222 Small cell lung cancer
    105491771
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    105491771
   05161 Hepatitis B
    105491771
   05160 Hepatitis C
    105491771
   05164 Influenza A
    105491771
   05162 Measles
    105491771
   05168 Herpes simplex virus 1 infection
    105491771
   05163 Human cytomegalovirus infection
    105491771
   05167 Kaposi sarcoma-associated herpesvirus infection
    105491771
   05169 Epstein-Barr virus infection
    105491771
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    105491771
   05134 Legionellosis
    105491771
   05152 Tuberculosis
    105491771
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    105491771
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105491771
   05012 Parkinson disease
    105491771
   05014 Amyotrophic lateral sclerosis
    105491771
   05016 Huntington disease
    105491771
   05017 Spinocerebellar ataxia
    105491771
   05020 Prion disease
    105491771
   05022 Pathways of neurodegeneration - multiple diseases
    105491771
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    105491771
   05416 Viral myocarditis
    105491771
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    105491771
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    105491771
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550
Other DBs
NCBI-GeneID: 105491771
NCBI-ProteinID: XP_011756738
Ensembl: ENSMNEG00000005674
UniProt: A0A2K6AQ26
LinkDB
Position
Unknown
AA seq 105 aa
MGDVEKGKKIFIMKCSQCHTVEKGSKHKIGPNLHGLFGRKTGQAPGCSYTAANKNKGNTW
GEDTLMEYLENPKKYIPGTKMICVGIKKKEERADLIAYLKKTTND
NT seq 318 nt   +upstreamnt  +downstreamnt
atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc
gttgaaaagggaagcaagcacaagattgggccaaatctccatggtctcttcgggaggaag
acaggtcaggcccctggatgctcttacacagccgccaataagaacaaaggcaacacctgg
ggagaggatacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatctgtgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa
aaaactactaatgactaa

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