Carlito syrichta (Philippine tarsier): 110596190 Help Entry 110596190         CDS       T07836                                  Name (RefSeq) cytochrome c, somatic-like   KO K08738   cytochrome c Organism csyr  Carlito syrichta (Philippine tarsier) Pathway csyr00190   Oxidative phosphorylation csyr01100   Metabolic pathways csyr01524   Platinum drug resistance csyr04115   p53 signaling pathway csyr04210   Apoptosis csyr04215   Apoptosis - multiple species csyr04932   Non-alcoholic fatty liver disease csyr05010   Alzheimer disease csyr05012   Parkinson disease csyr05014   Amyotrophic lateral sclerosis csyr05016   Huntington disease csyr05017   Spinocerebellar ataxia csyr05020   Prion disease csyr05022   Pathways of neurodegeneration - multiple diseases csyr05132   Salmonella infection csyr05134   Legionellosis csyr05145   Toxoplasmosis csyr05152   Tuberculosis csyr05160   Hepatitis C csyr05161   Hepatitis B csyr05162   Measles csyr05163   Human cytomegalovirus infection csyr05164   Influenza A csyr05167   Kaposi sarcoma-associated herpesvirus infection csyr05168   Herpes simplex virus 1 infection csyr05169   Epstein-Barr virus infection csyr05170   Human immunodeficiency virus 1 infection csyr05200   Pathways in cancer csyr05210   Colorectal cancer csyr05222   Small cell lung cancer csyr05416   Viral myocarditis csyr05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:csyr00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     110596190  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     110596190    04215 Apoptosis - multiple species     110596190    04115 p53 signaling pathway     110596190  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     110596190   09162 Cancer: specific types    05210 Colorectal cancer     110596190    05222 Small cell lung cancer     110596190   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     110596190    05161 Hepatitis B     110596190    05160 Hepatitis C     110596190    05164 Influenza A     110596190    05162 Measles     110596190    05168 Herpes simplex virus 1 infection     110596190    05163 Human cytomegalovirus infection     110596190    05167 Kaposi sarcoma-associated herpesvirus infection     110596190    05169 Epstein-Barr virus infection     110596190   09171 Infectious disease: bacterial    05132 Salmonella infection     110596190    05134 Legionellosis     110596190    05152 Tuberculosis     110596190   09174 Infectious disease: parasitic    05145 Toxoplasmosis     110596190   09164 Neurodegenerative disease    05010 Alzheimer disease     110596190    05012 Parkinson disease     110596190    05014 Amyotrophic lateral sclerosis     110596190    05016 Huntington disease     110596190    05017 Spinocerebellar ataxia     110596190    05020 Prion disease     110596190    05022 Pathways of neurodegeneration - multiple diseases     110596190   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     110596190    05416 Viral myocarditis     110596190   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     110596190   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     110596190 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  110596190 NCBI-ProteinID:  XP_021571146 UniProt:  A0A3Q0E6F4 LinkDB All DBs Position Unknown AA seq 109 aa AA seqDB search MGDVEKGKRIFVQKCAQCHTVEKEGKHKTGPNLHGLFGQKTGQAAGFSYTDTNKNKGITW GEDTLTEYLENPKNPWNKRIPGTKMIFEPGSKKGERADLIAYLKKATNE NT seq 330 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaggatttttgttcagaagtgtgcccagtgtcacact gtggaaaaggaaggcaagcacaagactgggccaaatctccatggtctttttgggcagaag acaggtcaggctgctggattctcttacacagacaccaataagaacaaaggcatcacctgg ggagaagataccctgacggagtatttggagaatcccaagaatccctggaacaaaagaatc cctggaacaaaaatgatctttgagccgggctcgaagaagggagaaagggcagacttgata gcttatctcaaaaaagctactaatgagtaa

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