Trachypithecus francoisi (Francois's langur): 117072825
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Entry
117072825 CDS
T07225
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
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Trachypithecus francoisi (Francois's langur)
Pathway
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Oxidative phosphorylation
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Metabolic pathways
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Platinum drug resistance
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p53 signaling pathway
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Apoptosis
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Apoptosis - multiple species
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Non-alcoholic fatty liver disease
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Alzheimer disease
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Parkinson disease
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Amyotrophic lateral sclerosis
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Huntington disease
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Spinocerebellar ataxia
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Prion disease
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Pathways of neurodegeneration - multiple diseases
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Salmonella infection
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Legionellosis
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Toxoplasmosis
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Tuberculosis
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Hepatitis C
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Hepatitis B
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Measles
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Human cytomegalovirus infection
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Influenza A
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Kaposi sarcoma-associated herpesvirus infection
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Herpes simplex virus 1 infection
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Epstein-Barr virus infection
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Human immunodeficiency virus 1 infection
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Pathways in cancer
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Colorectal cancer
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Small cell lung cancer
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Viral myocarditis
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Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
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]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
117072825
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
117072825
04215 Apoptosis - multiple species
117072825
04115 p53 signaling pathway
117072825
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
117072825
09162 Cancer: specific types
05210 Colorectal cancer
117072825
05222 Small cell lung cancer
117072825
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
117072825
05161 Hepatitis B
117072825
05160 Hepatitis C
117072825
05164 Influenza A
117072825
05162 Measles
117072825
05168 Herpes simplex virus 1 infection
117072825
05163 Human cytomegalovirus infection
117072825
05167 Kaposi sarcoma-associated herpesvirus infection
117072825
05169 Epstein-Barr virus infection
117072825
09171 Infectious disease: bacterial
05132 Salmonella infection
117072825
05134 Legionellosis
117072825
05152 Tuberculosis
117072825
09174 Infectious disease: parasitic
05145 Toxoplasmosis
117072825
09164 Neurodegenerative disease
05010 Alzheimer disease
117072825
05012 Parkinson disease
117072825
05014 Amyotrophic lateral sclerosis
117072825
05016 Huntington disease
117072825
05017 Spinocerebellar ataxia
117072825
05020 Prion disease
117072825
05022 Pathways of neurodegeneration - multiple diseases
117072825
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
117072825
05416 Viral myocarditis
117072825
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
117072825
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
117072825
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
117072825
NCBI-ProteinID:
XP_033049143
LinkDB
All DBs
Position
Unknown
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTAANKNKGITW
GEDTLMEYLENPTKYIPGTKMIFVGIKKKEERADLIAYLKKATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc
gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctcttcgggcggaag
acaggtcaggcccctggatactcttacacagccgccaataagaacaaaggcatcacctgg
ggagaggatacactgatggagtatttggagaatcccacgaagtacatccctggaacaaaa
atgatctttgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa
aaagctactaatgagtaa
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integrated database retrieval system