Puma yagouaroundi (jaguarundi): 121028606 Help Entry 121028606         CDS       T07555                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism pyu  Puma yagouaroundi (jaguarundi) Pathway pyu00190   Oxidative phosphorylation pyu01100   Metabolic pathways pyu01524   Platinum drug resistance pyu04115   p53 signaling pathway pyu04210   Apoptosis pyu04215   Apoptosis - multiple species pyu04932   Non-alcoholic fatty liver disease pyu05010   Alzheimer disease pyu05012   Parkinson disease pyu05014   Amyotrophic lateral sclerosis pyu05016   Huntington disease pyu05017   Spinocerebellar ataxia pyu05020   Prion disease pyu05022   Pathways of neurodegeneration - multiple diseases pyu05132   Salmonella infection pyu05134   Legionellosis pyu05145   Toxoplasmosis pyu05152   Tuberculosis pyu05160   Hepatitis C pyu05161   Hepatitis B pyu05162   Measles pyu05163   Human cytomegalovirus infection pyu05164   Influenza A pyu05167   Kaposi sarcoma-associated herpesvirus infection pyu05168   Herpes simplex virus 1 infection pyu05169   Epstein-Barr virus infection pyu05170   Human immunodeficiency virus 1 infection pyu05200   Pathways in cancer pyu05210   Colorectal cancer pyu05222   Small cell lung cancer pyu05416   Viral myocarditis pyu05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:pyu00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     121028606  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     121028606    04215 Apoptosis - multiple species     121028606    04115 p53 signaling pathway     121028606  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     121028606   09162 Cancer: specific types    05210 Colorectal cancer     121028606    05222 Small cell lung cancer     121028606   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     121028606    05161 Hepatitis B     121028606    05160 Hepatitis C     121028606    05164 Influenza A     121028606    05162 Measles     121028606    05168 Herpes simplex virus 1 infection     121028606    05163 Human cytomegalovirus infection     121028606    05167 Kaposi sarcoma-associated herpesvirus infection     121028606    05169 Epstein-Barr virus infection     121028606   09171 Infectious disease: bacterial    05132 Salmonella infection     121028606    05134 Legionellosis     121028606    05152 Tuberculosis     121028606   09174 Infectious disease: parasitic    05145 Toxoplasmosis     121028606   09164 Neurodegenerative disease    05010 Alzheimer disease     121028606    05012 Parkinson disease     121028606    05014 Amyotrophic lateral sclerosis     121028606    05016 Huntington disease     121028606    05017 Spinocerebellar ataxia     121028606    05020 Prion disease     121028606    05022 Pathways of neurodegeneration - multiple diseases     121028606   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     121028606    05416 Viral myocarditis     121028606   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     121028606   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     121028606 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  121028606 NCBI-ProteinID:  XP_040328344 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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