Cebus imitator (Panamanian white-faced capuchin): 108281951
Help
Entry
108281951 CDS
T08783
Name
(RefSeq) cytochrome c, somatic-like
KO
K08738
cytochrome c
Organism
cimi
Cebus imitator (Panamanian white-faced capuchin)
Pathway
cimi00190
Oxidative phosphorylation
cimi01100
Metabolic pathways
cimi01524
Platinum drug resistance
cimi04115
p53 signaling pathway
cimi04210
Apoptosis
cimi04215
Apoptosis - multiple species
cimi04932
Non-alcoholic fatty liver disease
cimi05010
Alzheimer disease
cimi05012
Parkinson disease
cimi05014
Amyotrophic lateral sclerosis
cimi05016
Huntington disease
cimi05017
Spinocerebellar ataxia
cimi05020
Prion disease
cimi05022
Pathways of neurodegeneration - multiple diseases
cimi05132
Salmonella infection
cimi05134
Legionellosis
cimi05145
Toxoplasmosis
cimi05152
Tuberculosis
cimi05160
Hepatitis C
cimi05161
Hepatitis B
cimi05162
Measles
cimi05163
Human cytomegalovirus infection
cimi05164
Influenza A
cimi05167
Kaposi sarcoma-associated herpesvirus infection
cimi05168
Herpes simplex virus 1 infection
cimi05169
Epstein-Barr virus infection
cimi05170
Human immunodeficiency virus 1 infection
cimi05200
Pathways in cancer
cimi05210
Colorectal cancer
cimi05222
Small cell lung cancer
cimi05416
Viral myocarditis
cimi05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
cimi00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
108281951
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
108281951
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
108281951
09162 Cancer: specific types
05210 Colorectal cancer
108281951
05222 Small cell lung cancer
108281951
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
108281951
05161 Hepatitis B
108281951
05160 Hepatitis C
108281951
05164 Influenza A
108281951
05162 Measles
108281951
05163 Human cytomegalovirus infection
108281951
05167 Kaposi sarcoma-associated herpesvirus infection
108281951
05169 Epstein-Barr virus infection
108281951
09171 Infectious disease: bacterial
05134 Legionellosis
108281951
05152 Tuberculosis
108281951
09174 Infectious disease: parasitic
05145 Toxoplasmosis
108281951
09164 Neurodegenerative disease
05010 Alzheimer disease
108281951
05012 Parkinson disease
108281951
05014 Amyotrophic lateral sclerosis
108281951
05016 Huntington disease
108281951
05017 Spinocerebellar ataxia
108281951
05020 Prion disease
108281951
05022 Pathways of neurodegeneration - multiple diseases
108281951
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
108281951
05416 Viral myocarditis
108281951
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
108281951
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
108281951
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Tox-HNH-EHHH
Motif
Other DBs
NCBI-GeneID:
108281951
NCBI-ProteinID:
XP_037583475
LinkDB
All DBs
Position
Unknown
AA seq
105 aa
AA seq
DB search
MGDVEKGKKICVQKCSQGHTVEKGGKHENGPNLHGIFGRKTGWAAGFSYTDANKNTDITW
GEDTLMEYLENPMKYILGTKVIFAGIKKKGERADLIAYLRKVTNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaaagggaagaaaatttgtgttcagaagtgttcccagggccacact
gtggaaaagggaggcaagcacgagaatgggcctaatctccatggtatctttgggcggaag
acaggttgggccgcgggattctcttacactgacgccaataagaacacagacatcacctgg
ggagaggatacattgatggagtatttggagaatcccatgaagtacatccttggaacaaaa
gtgatctttgccggcattaagaagaagggagaaagggcagacttgatagcttatctcaga
aaagttactaatgagtaa
DBGET
integrated database retrieval system