Talpa occidentalis (Iberian mole): 119243508
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Entry
119243508 CDS
T07495
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
tod
Talpa occidentalis (Iberian mole)
Pathway
tod00190
Oxidative phosphorylation
tod01100
Metabolic pathways
tod01524
Platinum drug resistance
tod04115
p53 signaling pathway
tod04210
Apoptosis
tod04215
Apoptosis - multiple species
tod04932
Non-alcoholic fatty liver disease
tod05010
Alzheimer disease
tod05012
Parkinson disease
tod05014
Amyotrophic lateral sclerosis
tod05016
Huntington disease
tod05017
Spinocerebellar ataxia
tod05020
Prion disease
tod05022
Pathways of neurodegeneration - multiple diseases
tod05132
Salmonella infection
tod05134
Legionellosis
tod05145
Toxoplasmosis
tod05152
Tuberculosis
tod05160
Hepatitis C
tod05161
Hepatitis B
tod05162
Measles
tod05163
Human cytomegalovirus infection
tod05164
Influenza A
tod05167
Kaposi sarcoma-associated herpesvirus infection
tod05168
Herpes simplex virus 1 infection
tod05169
Epstein-Barr virus infection
tod05170
Human immunodeficiency virus 1 infection
tod05200
Pathways in cancer
tod05210
Colorectal cancer
tod05222
Small cell lung cancer
tod05416
Viral myocarditis
tod05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
tod00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
119243508
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
119243508
04215 Apoptosis - multiple species
119243508
04115 p53 signaling pathway
119243508
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
119243508
09162 Cancer: specific types
05210 Colorectal cancer
119243508
05222 Small cell lung cancer
119243508
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
119243508
05161 Hepatitis B
119243508
05160 Hepatitis C
119243508
05164 Influenza A
119243508
05162 Measles
119243508
05168 Herpes simplex virus 1 infection
119243508
05163 Human cytomegalovirus infection
119243508
05167 Kaposi sarcoma-associated herpesvirus infection
119243508
05169 Epstein-Barr virus infection
119243508
09171 Infectious disease: bacterial
05132 Salmonella infection
119243508
05134 Legionellosis
119243508
05152 Tuberculosis
119243508
09174 Infectious disease: parasitic
05145 Toxoplasmosis
119243508
09164 Neurodegenerative disease
05010 Alzheimer disease
119243508
05012 Parkinson disease
119243508
05014 Amyotrophic lateral sclerosis
119243508
05016 Huntington disease
119243508
05017 Spinocerebellar ataxia
119243508
05020 Prion disease
119243508
05022 Pathways of neurodegeneration - multiple diseases
119243508
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
119243508
05416 Viral myocarditis
119243508
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
119243508
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
119243508
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
119243508
NCBI-ProteinID:
XP_037365313
LinkDB
All DBs
Position
Unknown
AA seq
105 aa
AA seq
DB search
MSDIEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
KEDTLMEYLENPKKYIPGTKMIFAGIKKKSERAELIAYLKKATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgagtgacattgagaagggcaagaagatttttgttcaaaagtgtgcccagtgccatact
gtggaaaagggaggcaagcacaaaactgggccaaatctccatggtctctttgggcgaaag
acaggtcaggcccctggattttcttacacagatgccaacaagaacaaaggcatcacctgg
aaagaggacacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagaagtcagaaagggcagagttgatagcttatctcaag
aaagctactaatgagtaa
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