Equus asinus (ass): 106829744 Help Entry 106829744         CDS       T04645                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism eai  Equus asinus (ass) Pathway eai00190   Oxidative phosphorylation eai01100   Metabolic pathways eai01524   Platinum drug resistance eai04115   p53 signaling pathway eai04210   Apoptosis eai04215   Apoptosis - multiple species eai04932   Non-alcoholic fatty liver disease eai05010   Alzheimer disease eai05012   Parkinson disease eai05014   Amyotrophic lateral sclerosis eai05016   Huntington disease eai05017   Spinocerebellar ataxia eai05020   Prion disease eai05022   Pathways of neurodegeneration - multiple diseases eai05132   Salmonella infection eai05134   Legionellosis eai05145   Toxoplasmosis eai05152   Tuberculosis eai05160   Hepatitis C eai05161   Hepatitis B eai05162   Measles eai05163   Human cytomegalovirus infection eai05164   Influenza A eai05167   Kaposi sarcoma-associated herpesvirus infection eai05168   Herpes simplex virus 1 infection eai05169   Epstein-Barr virus infection eai05170   Human immunodeficiency virus 1 infection eai05200   Pathways in cancer eai05210   Colorectal cancer eai05222   Small cell lung cancer eai05416   Viral myocarditis eai05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:eai00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     106829744  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     106829744    04215 Apoptosis - multiple species     106829744    04115 p53 signaling pathway     106829744  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     106829744   09162 Cancer: specific types    05210 Colorectal cancer     106829744    05222 Small cell lung cancer     106829744   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     106829744    05161 Hepatitis B     106829744    05160 Hepatitis C     106829744    05164 Influenza A     106829744    05162 Measles     106829744    05168 Herpes simplex virus 1 infection     106829744    05163 Human cytomegalovirus infection     106829744    05167 Kaposi sarcoma-associated herpesvirus infection     106829744    05169 Epstein-Barr virus infection     106829744   09171 Infectious disease: bacterial    05132 Salmonella infection     106829744    05134 Legionellosis     106829744    05152 Tuberculosis     106829744   09174 Infectious disease: parasitic    05145 Toxoplasmosis     106829744   09164 Neurodegenerative disease    05010 Alzheimer disease     106829744    05012 Parkinson disease     106829744    05014 Amyotrophic lateral sclerosis     106829744    05016 Huntington disease     106829744    05017 Spinocerebellar ataxia     106829744    05020 Prion disease     106829744    05022 Pathways of neurodegeneration - multiple diseases     106829744   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     106829744    05416 Viral myocarditis     106829744   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     106829744   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     106829744 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  106829744 NCBI-ProteinID:  XP_014694487 UniProt:  P68097 LinkDB All DBs Position 1:45666397..45668659 Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW KEETLMEYLENPKKYIPGTKMIFAGIKKKTEREDLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgacgttgagaagggcaagaagatttttgttcagaagtgcgcccagtgccatact gtggaaaagggaggcaagcacaagactgggccaaacctccatggtctatttgggcgaaag acgggtcaggcccctggcttctcttacacagatgccaacaagaacaaaggcatcacctgg aaagaggaaacactgatggaatatttggagaatcccaagaagtacatccctggaacaaaa atgatctttgctggcattaagaagaagacagaaagagaagatttaatagcttatctcaaa aaagctactaatgagtaa

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