Lemur catta (Ring-tailed lemur): 123638197
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Entry
123638197 CDS
T08326
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
lcat
Lemur catta (Ring-tailed lemur)
Pathway
lcat00190
Oxidative phosphorylation
lcat01100
Metabolic pathways
lcat01524
Platinum drug resistance
lcat04115
p53 signaling pathway
lcat04210
Apoptosis
lcat04215
Apoptosis - multiple species
lcat04932
Non-alcoholic fatty liver disease
lcat05010
Alzheimer disease
lcat05012
Parkinson disease
lcat05014
Amyotrophic lateral sclerosis
lcat05016
Huntington disease
lcat05017
Spinocerebellar ataxia
lcat05020
Prion disease
lcat05022
Pathways of neurodegeneration - multiple diseases
lcat05132
Salmonella infection
lcat05134
Legionellosis
lcat05145
Toxoplasmosis
lcat05152
Tuberculosis
lcat05160
Hepatitis C
lcat05161
Hepatitis B
lcat05162
Measles
lcat05163
Human cytomegalovirus infection
lcat05164
Influenza A
lcat05167
Kaposi sarcoma-associated herpesvirus infection
lcat05168
Herpes simplex virus 1 infection
lcat05169
Epstein-Barr virus infection
lcat05170
Human immunodeficiency virus 1 infection
lcat05200
Pathways in cancer
lcat05210
Colorectal cancer
lcat05222
Small cell lung cancer
lcat05416
Viral myocarditis
lcat05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
lcat00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
123638197
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
123638197
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
123638197
09162 Cancer: specific types
05210 Colorectal cancer
123638197
05222 Small cell lung cancer
123638197
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
123638197
05161 Hepatitis B
123638197
05160 Hepatitis C
123638197
05164 Influenza A
123638197
05162 Measles
123638197
05163 Human cytomegalovirus infection
123638197
05167 Kaposi sarcoma-associated herpesvirus infection
123638197
05169 Epstein-Barr virus infection
123638197
09171 Infectious disease: bacterial
05134 Legionellosis
123638197
05152 Tuberculosis
123638197
09174 Infectious disease: parasitic
05145 Toxoplasmosis
123638197
09164 Neurodegenerative disease
05010 Alzheimer disease
123638197
05012 Parkinson disease
123638197
05014 Amyotrophic lateral sclerosis
123638197
05016 Huntington disease
123638197
05017 Spinocerebellar ataxia
123638197
05020 Prion disease
123638197
05022 Pathways of neurodegeneration - multiple diseases
123638197
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
123638197
05416 Viral myocarditis
123638197
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
123638197
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
123638197
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Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Motif
Other DBs
NCBI-GeneID:
123638197
NCBI-ProteinID:
XP_045407587
LinkDB
All DBs
Position
5:42594036..42594361
Genome browser
AA seq
106 aa
AA seq
DB search
MGDVEKGKKIFVQKYAQGHTVEKGSKHKMSLGPNPHCLSGWRTGQAVGFSYTDANKNRDI
TWGEDILMEYLENPKKYIPGTKVIFAGVKKVERADLIAYLKRVTNE
NT seq
321 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaaaggcaagaagatttttgttcagaagtatgcccagggtcacact
gtggaaaagggaagcaagcacaagatgagtctgggtccaaatccccattgtctctctggg
tggaggacaggtcaggctgttggattctcttatacagatgccaataagaacagagacatc
acctggggagaggatatactcatggagtatttggagaatcccaagaagtacatccctgga
acaaaagtgatctttgctggagttaagaaggtagaaagggcagacttgatagcttatctc
aaaagagttactaatgagtaa
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