Ursus arctos (brown bear): 113263367 Help Entry 113263367         CDS       T05909                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism uah  Ursus arctos (brown bear) Pathway uah00190   Oxidative phosphorylation uah01100   Metabolic pathways uah01524   Platinum drug resistance uah04115   p53 signaling pathway uah04210   Apoptosis uah04215   Apoptosis - multiple species uah04932   Non-alcoholic fatty liver disease uah05010   Alzheimer disease uah05012   Parkinson disease uah05014   Amyotrophic lateral sclerosis uah05016   Huntington disease uah05017   Spinocerebellar ataxia uah05020   Prion disease uah05022   Pathways of neurodegeneration - multiple diseases uah05132   Salmonella infection uah05134   Legionellosis uah05145   Toxoplasmosis uah05152   Tuberculosis uah05160   Hepatitis C uah05161   Hepatitis B uah05162   Measles uah05163   Human cytomegalovirus infection uah05164   Influenza A uah05167   Kaposi sarcoma-associated herpesvirus infection uah05168   Herpes simplex virus 1 infection uah05169   Epstein-Barr virus infection uah05170   Human immunodeficiency virus 1 infection uah05200   Pathways in cancer uah05210   Colorectal cancer uah05222   Small cell lung cancer uah05416   Viral myocarditis uah05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:uah00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     113263367  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     113263367    04215 Apoptosis - multiple species     113263367    04115 p53 signaling pathway     113263367  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     113263367   09162 Cancer: specific types    05210 Colorectal cancer     113263367    05222 Small cell lung cancer     113263367   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     113263367    05161 Hepatitis B     113263367    05160 Hepatitis C     113263367    05164 Influenza A     113263367    05162 Measles     113263367    05168 Herpes simplex virus 1 infection     113263367    05163 Human cytomegalovirus infection     113263367    05167 Kaposi sarcoma-associated herpesvirus infection     113263367    05169 Epstein-Barr virus infection     113263367   09171 Infectious disease: bacterial    05132 Salmonella infection     113263367    05134 Legionellosis     113263367    05152 Tuberculosis     113263367   09174 Infectious disease: parasitic    05145 Toxoplasmosis     113263367   09164 Neurodegenerative disease    05010 Alzheimer disease     113263367    05012 Parkinson disease     113263367    05014 Amyotrophic lateral sclerosis     113263367    05016 Huntington disease     113263367    05017 Spinocerebellar ataxia     113263367    05020 Prion disease     113263367    05022 Pathways of neurodegeneration - multiple diseases     113263367   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     113263367    05416 Viral myocarditis     113263367   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     113263367   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     113263367 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Motif Other DBs NCBI-GeneID:  113263367 NCBI-ProteinID:  XP_048069860 LinkDB All DBs Position Unknown AA seq 101 aa AA seqDB search MGGVEKDKKIFIPKNLCHTVEKGGKHKTGPNLRGLFGRKTGQAPGFSYRDANKNEGITLG EETPMEYLENPKSSPGTEMIFSGIKKTGERADLIADLKKSY NT seq 306 nt NT seq  +upstreamnt  +downstreamnt atgggtggtgttgagaaggacaagaagatttttattccaaaaaatctgtgccatactgtg gaaaagggaggcaagcacaagactgggccaaatctccgtggtttatttgggagaaagaca ggtcaggcccctggattttcttacagggatgccaacaagaacgaaggcatcaccttggga gaggagacaccgatggagtatttggagaatcccaagtccagccctggaacagaaatgatc ttctctggtattaagaagacaggggaaagggcagacttgatagctgatctcaaaaaaagc tactaa

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