Acinonyx jubatus (cheetah): 106973875
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Entry
106973875 CDS
T04657
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
aju
Acinonyx jubatus (cheetah)
Pathway
aju00190
Oxidative phosphorylation
aju01100
Metabolic pathways
aju01524
Platinum drug resistance
aju04115
p53 signaling pathway
aju04210
Apoptosis
aju04215
Apoptosis - multiple species
aju04932
Non-alcoholic fatty liver disease
aju05010
Alzheimer disease
aju05012
Parkinson disease
aju05014
Amyotrophic lateral sclerosis
aju05016
Huntington disease
aju05017
Spinocerebellar ataxia
aju05020
Prion disease
aju05022
Pathways of neurodegeneration - multiple diseases
aju05132
Salmonella infection
aju05134
Legionellosis
aju05145
Toxoplasmosis
aju05152
Tuberculosis
aju05160
Hepatitis C
aju05161
Hepatitis B
aju05162
Measles
aju05163
Human cytomegalovirus infection
aju05164
Influenza A
aju05167
Kaposi sarcoma-associated herpesvirus infection
aju05168
Herpes simplex virus 1 infection
aju05169
Epstein-Barr virus infection
aju05170
Human immunodeficiency virus 1 infection
aju05200
Pathways in cancer
aju05210
Colorectal cancer
aju05222
Small cell lung cancer
aju05416
Viral myocarditis
aju05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
aju00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
106973875
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
106973875
04215 Apoptosis - multiple species
106973875
04115 p53 signaling pathway
106973875
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
106973875
09162 Cancer: specific types
05210 Colorectal cancer
106973875
05222 Small cell lung cancer
106973875
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
106973875
05161 Hepatitis B
106973875
05160 Hepatitis C
106973875
05164 Influenza A
106973875
05162 Measles
106973875
05168 Herpes simplex virus 1 infection
106973875
05163 Human cytomegalovirus infection
106973875
05167 Kaposi sarcoma-associated herpesvirus infection
106973875
05169 Epstein-Barr virus infection
106973875
09171 Infectious disease: bacterial
05132 Salmonella infection
106973875
05134 Legionellosis
106973875
05152 Tuberculosis
106973875
09174 Infectious disease: parasitic
05145 Toxoplasmosis
106973875
09164 Neurodegenerative disease
05010 Alzheimer disease
106973875
05012 Parkinson disease
106973875
05014 Amyotrophic lateral sclerosis
106973875
05016 Huntington disease
106973875
05017 Spinocerebellar ataxia
106973875
05020 Prion disease
106973875
05022 Pathways of neurodegeneration - multiple diseases
106973875
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
106973875
05416 Viral myocarditis
106973875
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
106973875
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
106973875
BRITE hierarchy
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
106973875
NCBI-ProteinID:
XP_053077170
LinkDB
All DBs
Position
C2:87875695..87876319
Genome browser
AA seq
94 aa
AA seq
DB search
MGDVEKGKEIFVQKCAQCHTVGKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNNGITW
GEETLMEYLENPKKYIPGTKMIFAVIKRQGKEQA
NT seq
285 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaaggagatttttgttcagaagtgtgcccagtgccatact
gtgggaaagggaggcaagcataagactgggccaaatctccatggtttatttgggcgaaag
acaggtcaagcccctggattttcttacacggatgccaacaagaacaatggcatcacctgg
ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctgtcattaaaaggcaggggaaagagcaggcttga
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