Loxodonta africana (African savanna elephant): 100657132
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Entry
100657132 CDS
T04351
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
lav
Loxodonta africana (African savanna elephant)
Pathway
lav00190
Oxidative phosphorylation
lav01100
Metabolic pathways
lav01524
Platinum drug resistance
lav04115
p53 signaling pathway
lav04210
Apoptosis
lav04215
Apoptosis - multiple species
lav04932
Non-alcoholic fatty liver disease
lav05010
Alzheimer disease
lav05012
Parkinson disease
lav05014
Amyotrophic lateral sclerosis
lav05016
Huntington disease
lav05017
Spinocerebellar ataxia
lav05020
Prion disease
lav05022
Pathways of neurodegeneration - multiple diseases
lav05132
Salmonella infection
lav05134
Legionellosis
lav05145
Toxoplasmosis
lav05152
Tuberculosis
lav05160
Hepatitis C
lav05161
Hepatitis B
lav05162
Measles
lav05163
Human cytomegalovirus infection
lav05164
Influenza A
lav05167
Kaposi sarcoma-associated herpesvirus infection
lav05168
Herpes simplex virus 1 infection
lav05169
Epstein-Barr virus infection
lav05170
Human immunodeficiency virus 1 infection
lav05200
Pathways in cancer
lav05210
Colorectal cancer
lav05222
Small cell lung cancer
lav05416
Viral myocarditis
lav05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
lav00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
100657132
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
100657132
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100657132
09162 Cancer: specific types
05210 Colorectal cancer
100657132
05222 Small cell lung cancer
100657132
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100657132
05161 Hepatitis B
100657132
05160 Hepatitis C
100657132
05164 Influenza A
100657132
05162 Measles
100657132
05163 Human cytomegalovirus infection
100657132
05167 Kaposi sarcoma-associated herpesvirus infection
100657132
05169 Epstein-Barr virus infection
100657132
09171 Infectious disease: bacterial
05134 Legionellosis
100657132
05152 Tuberculosis
100657132
09174 Infectious disease: parasitic
05145 Toxoplasmosis
100657132
09164 Neurodegenerative disease
05010 Alzheimer disease
100657132
05012 Parkinson disease
100657132
05014 Amyotrophic lateral sclerosis
100657132
05016 Huntington disease
100657132
05017 Spinocerebellar ataxia
100657132
05020 Prion disease
100657132
05022 Pathways of neurodegeneration - multiple diseases
100657132
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100657132
05416 Viral myocarditis
100657132
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
100657132
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100657132
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Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
Motif
Other DBs
NCBI-GeneID:
100657132
NCBI-ProteinID:
XP_003407118
UniProt:
G3SZ22
LinkDB
All DBs
Position
Unknown
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEDTLMEYLENPKKYIPGTKMIFAGIKKKAERADLIAYLKQATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgtcgagaagggcaagaagatttttgttcagaaatgttcccagtgccacaca
gtggaaaagggaggcaagcacaagactgggccaaatctgcacggcttgtttgggcggaag
actggtcaagcccctggattctcttacacggatgccaataagaacaaaggtatcacctgg
ggagaggacacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatctttgctggcattaagaagaaggcagaaagggcagacttgatagcttatctcaag
caagctactaatgagtaa
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