KEGG   Physeter catodon (sperm whale): 102986675
Entry
102986675         CDS       T06011                                 
Name
(RefSeq) cytochrome c-like
  KO
K08738  cytochrome c
Organism
pcad  Physeter catodon (sperm whale)
Pathway
pcad00190  Oxidative phosphorylation
pcad01100  Metabolic pathways
pcad01524  Platinum drug resistance
pcad04115  p53 signaling pathway
pcad04210  Apoptosis
pcad04215  Apoptosis - multiple species
pcad04932  Non-alcoholic fatty liver disease
pcad05010  Alzheimer disease
pcad05012  Parkinson disease
pcad05014  Amyotrophic lateral sclerosis
pcad05016  Huntington disease
pcad05017  Spinocerebellar ataxia
pcad05020  Prion disease
pcad05022  Pathways of neurodegeneration - multiple diseases
pcad05132  Salmonella infection
pcad05134  Legionellosis
pcad05145  Toxoplasmosis
pcad05152  Tuberculosis
pcad05160  Hepatitis C
pcad05161  Hepatitis B
pcad05162  Measles
pcad05163  Human cytomegalovirus infection
pcad05164  Influenza A
pcad05167  Kaposi sarcoma-associated herpesvirus infection
pcad05168  Herpes simplex virus 1 infection
pcad05169  Epstein-Barr virus infection
pcad05170  Human immunodeficiency virus 1 infection
pcad05200  Pathways in cancer
pcad05210  Colorectal cancer
pcad05222  Small cell lung cancer
pcad05416  Viral myocarditis
pcad05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:pcad00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    102986675
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    102986675
   04215 Apoptosis - multiple species
    102986675
   04115 p53 signaling pathway
    102986675
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102986675
  09162 Cancer: specific types
   05210 Colorectal cancer
    102986675
   05222 Small cell lung cancer
    102986675
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    102986675
   05161 Hepatitis B
    102986675
   05160 Hepatitis C
    102986675
   05164 Influenza A
    102986675
   05162 Measles
    102986675
   05168 Herpes simplex virus 1 infection
    102986675
   05163 Human cytomegalovirus infection
    102986675
   05167 Kaposi sarcoma-associated herpesvirus infection
    102986675
   05169 Epstein-Barr virus infection
    102986675
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    102986675
   05134 Legionellosis
    102986675
   05152 Tuberculosis
    102986675
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    102986675
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102986675
   05012 Parkinson disease
    102986675
   05014 Amyotrophic lateral sclerosis
    102986675
   05016 Huntington disease
    102986675
   05017 Spinocerebellar ataxia
    102986675
   05020 Prion disease
    102986675
   05022 Pathways of neurodegeneration - multiple diseases
    102986675
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    102986675
   05416 Viral myocarditis
    102986675
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    102986675
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    102986675
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG
Other DBs
NCBI-GeneID: 102986675
NCBI-ProteinID: XP_007118006
Ensembl: ENSPCTG00005016773
UniProt: A0A2Y9F9I0
LinkDB
Position
13:complement(8439817..8440670)
AA seq 105 aa
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPSLHGLFGRKTGQAVGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKKGERADLIAYLKKATNE
NT seq 318 nt   +upstreamnt  +downstreamnt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact
gtggaaaagggaggcaagcacaagactgggccaagtctccatggtctgtttgggcgaaag
acaggtcaggctgtcggattctcttacacagatgccaacaagaacaaaggcatcacctgg
ggagaggagacgctgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagaagggagaaagggcagacttgatagcttatctcaaa
aaagctactaatgagtaa

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