Acinonyx jubatus (cheetah): 106982840 Help Entry 106982840         CDS       T04657                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism aju  Acinonyx jubatus (cheetah) Pathway aju00190   Oxidative phosphorylation aju01100   Metabolic pathways aju01524   Platinum drug resistance aju04115   p53 signaling pathway aju04210   Apoptosis aju04215   Apoptosis - multiple species aju04932   Non-alcoholic fatty liver disease aju05010   Alzheimer disease aju05012   Parkinson disease aju05014   Amyotrophic lateral sclerosis aju05016   Huntington disease aju05017   Spinocerebellar ataxia aju05020   Prion disease aju05022   Pathways of neurodegeneration - multiple diseases aju05132   Salmonella infection aju05134   Legionellosis aju05145   Toxoplasmosis aju05152   Tuberculosis aju05160   Hepatitis C aju05161   Hepatitis B aju05162   Measles aju05163   Human cytomegalovirus infection aju05164   Influenza A aju05167   Kaposi sarcoma-associated herpesvirus infection aju05168   Herpes simplex virus 1 infection aju05169   Epstein-Barr virus infection aju05170   Human immunodeficiency virus 1 infection aju05200   Pathways in cancer aju05210   Colorectal cancer aju05222   Small cell lung cancer aju05416   Viral myocarditis aju05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:aju00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     106982840  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     106982840    04215 Apoptosis - multiple species     106982840    04115 p53 signaling pathway     106982840  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     106982840   09162 Cancer: specific types    05210 Colorectal cancer     106982840    05222 Small cell lung cancer     106982840   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     106982840    05161 Hepatitis B     106982840    05160 Hepatitis C     106982840    05164 Influenza A     106982840    05162 Measles     106982840    05168 Herpes simplex virus 1 infection     106982840    05163 Human cytomegalovirus infection     106982840    05167 Kaposi sarcoma-associated herpesvirus infection     106982840    05169 Epstein-Barr virus infection     106982840   09171 Infectious disease: bacterial    05132 Salmonella infection     106982840    05134 Legionellosis     106982840    05152 Tuberculosis     106982840   09174 Infectious disease: parasitic    05145 Toxoplasmosis     106982840   09164 Neurodegenerative disease    05010 Alzheimer disease     106982840    05012 Parkinson disease     106982840    05014 Amyotrophic lateral sclerosis     106982840    05016 Huntington disease     106982840    05017 Spinocerebellar ataxia     106982840    05020 Prion disease     106982840    05022 Pathways of neurodegeneration - multiple diseases     106982840   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     106982840    05416 Viral myocarditis     106982840   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     106982840   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     106982840 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  106982840 NCBI-ProteinID:  XP_014936499 UniProt:  A0A6J0A3J4 LinkDB All DBs Position A2:51350000..51352488 Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKAGERADLIAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact gtggaaaagggaggcaagcacaagactgggccaaatctccacggtttatttgggcgaaag acaggccaagcccctgggttttcttacacggatgccaacaagaacaaaggcatcacctgg ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatcttcgctggcattaagaaggcaggggaaagagcagacttgatagcttatctcaaa aaagctactaaggagtaa

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