Hyaena hyaena (striped hyena): 120236951
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Entry
120236951 CDS
T07257
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
hhv
Hyaena hyaena (striped hyena)
Pathway
hhv00190
Oxidative phosphorylation
hhv01100
Metabolic pathways
hhv01524
Platinum drug resistance
hhv04115
p53 signaling pathway
hhv04210
Apoptosis
hhv04215
Apoptosis - multiple species
hhv04932
Non-alcoholic fatty liver disease
hhv05010
Alzheimer disease
hhv05012
Parkinson disease
hhv05014
Amyotrophic lateral sclerosis
hhv05016
Huntington disease
hhv05017
Spinocerebellar ataxia
hhv05020
Prion disease
hhv05022
Pathways of neurodegeneration - multiple diseases
hhv05132
Salmonella infection
hhv05134
Legionellosis
hhv05145
Toxoplasmosis
hhv05152
Tuberculosis
hhv05160
Hepatitis C
hhv05161
Hepatitis B
hhv05162
Measles
hhv05163
Human cytomegalovirus infection
hhv05164
Influenza A
hhv05167
Kaposi sarcoma-associated herpesvirus infection
hhv05168
Herpes simplex virus 1 infection
hhv05169
Epstein-Barr virus infection
hhv05170
Human immunodeficiency virus 1 infection
hhv05200
Pathways in cancer
hhv05210
Colorectal cancer
hhv05222
Small cell lung cancer
hhv05416
Viral myocarditis
hhv05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
hhv00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
120236951
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
120236951
04215 Apoptosis - multiple species
120236951
04115 p53 signaling pathway
120236951
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
120236951
09162 Cancer: specific types
05210 Colorectal cancer
120236951
05222 Small cell lung cancer
120236951
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
120236951
05161 Hepatitis B
120236951
05160 Hepatitis C
120236951
05164 Influenza A
120236951
05162 Measles
120236951
05168 Herpes simplex virus 1 infection
120236951
05163 Human cytomegalovirus infection
120236951
05167 Kaposi sarcoma-associated herpesvirus infection
120236951
05169 Epstein-Barr virus infection
120236951
09171 Infectious disease: bacterial
05132 Salmonella infection
120236951
05134 Legionellosis
120236951
05152 Tuberculosis
120236951
09174 Infectious disease: parasitic
05145 Toxoplasmosis
120236951
09164 Neurodegenerative disease
05010 Alzheimer disease
120236951
05012 Parkinson disease
120236951
05014 Amyotrophic lateral sclerosis
120236951
05016 Huntington disease
120236951
05017 Spinocerebellar ataxia
120236951
05020 Prion disease
120236951
05022 Pathways of neurodegeneration - multiple diseases
120236951
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
120236951
05416 Viral myocarditis
120236951
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
120236951
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
120236951
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
120236951
NCBI-ProteinID:
XP_039095989
LinkDB
All DBs
Position
Unknown
AA seq
132 aa
AA seq
DB search
MKKVERAGRPAWERAPSLRARPKSDLKMGDVEKGRKIFVQKCAQCHTVEKGGKHKTGPNL
HGLFGQKTGQAPGFSYTDANKNKGITWGEETLMEYLENPKKYIPGTKMIFAGVKKAGERA
DLIVYLKKATKE
NT seq
399 nt
NT seq
+upstream
nt +downstream
nt
atgaagaaagtggagagagctggacgtccggcttgggagcgggcaccttcgcttcgcgcg
cgaccaaagagcgatttaaaaatgggtgatgttgagaaaggcaggaagatttttgttcag
aagtgtgcccagtgccataccgtggaaaagggaggcaaacacaagacggggccaaatctc
catggtttatttgggcaaaaaacgggtcaagcccctggattttcttacacggatgccaac
aagaacaaaggcatcacctggggagaggagacactgatggagtatttggagaatcccaag
aagtacatcccaggaacaaaaatgatcttcgctggcgttaagaaggcaggggaaagagca
gacttgatagtttatctcaaaaaagctactaaggagtaa
DBGET
integrated database retrieval system