Acinonyx jubatus (cheetah): 106986613 Help Entry 106986613         CDS       T04657                                  Name (RefSeq) cytochrome c-like   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     106986613  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     106986613    04215 Apoptosis - multiple species     106986613    04115 p53 signaling pathway     106986613  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     106986613   09162 Cancer: specific types    05210 Colorectal cancer     106986613    05222 Small cell lung cancer     106986613   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     106986613    05161 Hepatitis B     106986613    05160 Hepatitis C     106986613    05164 Influenza A     106986613    05162 Measles     106986613    05168 Herpes simplex virus 1 infection     106986613    05163 Human cytomegalovirus infection     106986613    05167 Kaposi sarcoma-associated herpesvirus infection     106986613    05169 Epstein-Barr virus infection     106986613   09171 Infectious disease: bacterial    05132 Salmonella infection     106986613    05134 Legionellosis     106986613    05152 Tuberculosis     106986613   09174 Infectious disease: parasitic    05145 Toxoplasmosis     106986613   09164 Neurodegenerative disease    05010 Alzheimer disease     106986613    05012 Parkinson disease     106986613    05014 Amyotrophic lateral sclerosis     106986613    05016 Huntington disease     106986613    05017 Spinocerebellar ataxia     106986613    05020 Prion disease     106986613    05022 Pathways of neurodegeneration - multiple diseases     106986613   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     106986613    05416 Viral myocarditis     106986613   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     106986613   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     106986613 SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C PPAK Motif Other DBs NCBI-GeneID:  106986613 NCBI-ProteinID:  XP_026890797 UniProt:  A0A6J1XE98 LinkDB All DBs Position 12 Genome browser AA seq 93 aa AA seqDB search MGDVEQGKIFVQKCAQRHDAEKGGKHKTGPNLHGLFGWKAGQTPGFSYMDANQTKGTSWG EETLMKYLENPKKYIPETKMIFAGIKKARERAD NT seq 282 nt NT seq  +upstreamnt  +downstreamnt atgggtgacgttgagcagggcaagatttttgttcagaagtgtgcccagcgccatgacgcg gaaaagggcggcaagcacaagactgggccaaatctccatggtttatttgggtggaaggca ggtcaaacccctggattttcttacatggatgccaaccagaccaaaggcacctcctgggga gaggagacactgatgaagtatttggagaatcccaagaagtacatccctgaaacaaaaatg atctttgctggcattaagaaggcaagggaaagagcagactag

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