KEGG   Monodelphis domestica (gray short-tailed opossum): 100010620
Entry
100010620         CDS       T01031                                 
Name
(RefSeq) cytochrome c
  KO
K08738  cytochrome c
Organism
mdo  Monodelphis domestica (gray short-tailed opossum)
Pathway
mdo00190  Oxidative phosphorylation
mdo01100  Metabolic pathways
mdo01524  Platinum drug resistance
mdo04115  p53 signaling pathway
mdo04210  Apoptosis
mdo04215  Apoptosis - multiple species
mdo04932  Non-alcoholic fatty liver disease
mdo05010  Alzheimer disease
mdo05012  Parkinson disease
mdo05014  Amyotrophic lateral sclerosis
mdo05016  Huntington disease
mdo05017  Spinocerebellar ataxia
mdo05020  Prion disease
mdo05022  Pathways of neurodegeneration - multiple diseases
mdo05132  Salmonella infection
mdo05134  Legionellosis
mdo05145  Toxoplasmosis
mdo05152  Tuberculosis
mdo05160  Hepatitis C
mdo05161  Hepatitis B
mdo05162  Measles
mdo05163  Human cytomegalovirus infection
mdo05164  Influenza A
mdo05167  Kaposi sarcoma-associated herpesvirus infection
mdo05168  Herpes simplex virus 1 infection
mdo05169  Epstein-Barr virus infection
mdo05170  Human immunodeficiency virus 1 infection
mdo05200  Pathways in cancer
mdo05210  Colorectal cancer
mdo05222  Small cell lung cancer
mdo05416  Viral myocarditis
mdo05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:mdo00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    100010620
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    100010620
   04215 Apoptosis - multiple species
    100010620
   04115 p53 signaling pathway
    100010620
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100010620
  09162 Cancer: specific types
   05210 Colorectal cancer
    100010620
   05222 Small cell lung cancer
    100010620
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    100010620
   05161 Hepatitis B
    100010620
   05160 Hepatitis C
    100010620
   05164 Influenza A
    100010620
   05162 Measles
    100010620
   05168 Herpes simplex virus 1 infection
    100010620
   05163 Human cytomegalovirus infection
    100010620
   05167 Kaposi sarcoma-associated herpesvirus infection
    100010620
   05169 Epstein-Barr virus infection
    100010620
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    100010620
   05134 Legionellosis
    100010620
   05152 Tuberculosis
    100010620
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    100010620
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100010620
   05012 Parkinson disease
    100010620
   05014 Amyotrophic lateral sclerosis
    100010620
   05016 Huntington disease
    100010620
   05017 Spinocerebellar ataxia
    100010620
   05020 Prion disease
    100010620
   05022 Pathways of neurodegeneration - multiple diseases
    100010620
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    100010620
   05416 Viral myocarditis
    100010620
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    100010620
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    100010620
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG
Other DBs
NCBI-GeneID: 100010620
NCBI-ProteinID: XP_001363248
Ensembl: ENSMODG00000000653
UniProt: A0A5F8HEK2
LinkDB
Position
8:299069490..299071652
AA seq 105 aa
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLNGLFGRKTGQAPGFSYTDANKSKGIIW
SEDTLMEYLENPKKYIPGTKMIFAGIKKKGERADLIAYLKKATNE
NT seq 318 nt   +upstreamnt  +downstreamnt
atgggagacgtggagaagggcaagaagattttcgtgcagaagtgtgcccagtgccacacg
gtggagaaggggggcaagcacaagactgggcccaacctgaatggccttttcggccgcaag
actggccaggcccctggtttctcctacacggatgccaacaaaagcaaagggatcatctgg
agtgaagacacgttgatggagtacttggaaaatcccaagaagtacatcccgggtacaaag
atgattttcgcaggcattaagaagaagggggagagagcagacttgatagcctacctgaag
aaagccaccaacgagtaa

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