Puma concolor (puma): 112866541 Help Entry 112866541         CDS       T08890                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism pcoo  Puma concolor (puma) Pathway pcoo00190   Oxidative phosphorylation pcoo01100   Metabolic pathways pcoo01524   Platinum drug resistance pcoo04115   p53 signaling pathway pcoo04210   Apoptosis pcoo04215   Apoptosis - multiple species pcoo04932   Non-alcoholic fatty liver disease pcoo05010   Alzheimer disease pcoo05012   Parkinson disease pcoo05014   Amyotrophic lateral sclerosis pcoo05016   Huntington disease pcoo05017   Spinocerebellar ataxia pcoo05020   Prion disease pcoo05022   Pathways of neurodegeneration - multiple diseases pcoo05132   Salmonella infection pcoo05134   Legionellosis pcoo05145   Toxoplasmosis pcoo05152   Tuberculosis pcoo05160   Hepatitis C pcoo05161   Hepatitis B pcoo05162   Measles pcoo05163   Human cytomegalovirus infection pcoo05164   Influenza A pcoo05167   Kaposi sarcoma-associated herpesvirus infection pcoo05168   Herpes simplex virus 1 infection pcoo05169   Epstein-Barr virus infection pcoo05170   Human immunodeficiency virus 1 infection pcoo05200   Pathways in cancer pcoo05210   Colorectal cancer pcoo05222   Small cell lung cancer pcoo05416   Viral myocarditis pcoo05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:pcoo00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     112866541  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     112866541    04215 Apoptosis - multiple species     112866541    04115 p53 signaling pathway     112866541  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112866541   09162 Cancer: specific types    05210 Colorectal cancer     112866541    05222 Small cell lung cancer     112866541   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     112866541    05161 Hepatitis B     112866541    05160 Hepatitis C     112866541    05164 Influenza A     112866541    05162 Measles     112866541    05168 Herpes simplex virus 1 infection     112866541    05163 Human cytomegalovirus infection     112866541    05167 Kaposi sarcoma-associated herpesvirus infection     112866541    05169 Epstein-Barr virus infection     112866541   09171 Infectious disease: bacterial    05132 Salmonella infection     112866541    05134 Legionellosis     112866541    05152 Tuberculosis     112866541   09174 Infectious disease: parasitic    05145 Toxoplasmosis     112866541   09164 Neurodegenerative disease    05010 Alzheimer disease     112866541    05012 Parkinson disease     112866541    05014 Amyotrophic lateral sclerosis     112866541    05016 Huntington disease     112866541    05017 Spinocerebellar ataxia     112866541    05020 Prion disease     112866541    05022 Pathways of neurodegeneration - multiple diseases     112866541   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     112866541    05416 Viral myocarditis     112866541   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     112866541   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     112866541 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  112866541 NCBI-ProteinID:  XP_025785218 UniProt:  A0A6P6IC08 LinkDB All DBs Position Unknown 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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