Leptonychotes weddellii (Weddell seal): 102726669 Help Entry 102726669         CDS       T08708                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism lww  Leptonychotes weddellii (Weddell seal) Pathway lww00190   Oxidative phosphorylation lww01100   Metabolic pathways lww01524   Platinum drug resistance lww04115   p53 signaling pathway lww04210   Apoptosis lww04215   Apoptosis - multiple species lww04932   Non-alcoholic fatty liver disease lww05010   Alzheimer disease lww05012   Parkinson disease lww05014   Amyotrophic lateral sclerosis lww05016   Huntington disease lww05017   Spinocerebellar ataxia lww05020   Prion disease lww05022   Pathways of neurodegeneration - multiple diseases lww05132   Salmonella infection lww05134   Legionellosis lww05145   Toxoplasmosis lww05152   Tuberculosis lww05160   Hepatitis C lww05161   Hepatitis B lww05162   Measles lww05163   Human cytomegalovirus infection lww05164   Influenza A lww05167   Kaposi sarcoma-associated herpesvirus infection lww05168   Herpes simplex virus 1 infection lww05169   Epstein-Barr virus infection lww05170   Human immunodeficiency virus 1 infection lww05200   Pathways in cancer lww05210   Colorectal cancer lww05222   Small cell lung cancer lww05416   Viral myocarditis lww05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:lww00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     102726669  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     102726669    04215 Apoptosis - multiple species     102726669    04115 p53 signaling pathway     102726669  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102726669   09162 Cancer: specific types    05210 Colorectal cancer     102726669    05222 Small cell lung cancer     102726669   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     102726669    05161 Hepatitis B     102726669    05160 Hepatitis C     102726669    05164 Influenza A     102726669    05162 Measles     102726669    05168 Herpes simplex virus 1 infection     102726669    05163 Human cytomegalovirus infection     102726669    05167 Kaposi sarcoma-associated herpesvirus infection     102726669    05169 Epstein-Barr virus infection     102726669   09171 Infectious disease: bacterial    05132 Salmonella infection     102726669    05134 Legionellosis     102726669    05152 Tuberculosis     102726669   09174 Infectious disease: parasitic    05145 Toxoplasmosis     102726669   09164 Neurodegenerative disease    05010 Alzheimer disease     102726669    05012 Parkinson disease     102726669    05014 Amyotrophic lateral sclerosis     102726669    05016 Huntington disease     102726669    05017 Spinocerebellar ataxia     102726669    05020 Prion disease     102726669    05022 Pathways of neurodegeneration - multiple diseases     102726669   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     102726669    05416 Viral myocarditis     102726669   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     102726669   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     102726669 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  102726669 NCBI-ProteinID:  XP_006748918 UniProt:  A0A2U3XXZ4 LinkDB All DBs Position Unknown AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKTGERADLIAYLKVATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccaatgccatacc gtggaaaagggaggcaagcacaagactgggccaaatctccatggtttatttggccgaaag acaggtcaggcccctggattttcttacacggatgccaacaagaacaaaggcatcacctgg ggagaagagacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatcttcgctggcattaagaagacaggggaaagagcagacttgatagcttatctcaaa gtagctactaaggagtaa

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