Ursus maritimus (polar bear): 103658902
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Entry
103658902 CDS
T03271
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
umr
Ursus maritimus (polar bear)
Pathway
umr00190
Oxidative phosphorylation
umr01100
Metabolic pathways
umr01524
Platinum drug resistance
umr04115
p53 signaling pathway
umr04210
Apoptosis
umr04215
Apoptosis - multiple species
umr04932
Non-alcoholic fatty liver disease
umr05010
Alzheimer disease
umr05012
Parkinson disease
umr05014
Amyotrophic lateral sclerosis
umr05016
Huntington disease
umr05017
Spinocerebellar ataxia
umr05020
Prion disease
umr05022
Pathways of neurodegeneration - multiple diseases
umr05132
Salmonella infection
umr05134
Legionellosis
umr05145
Toxoplasmosis
umr05152
Tuberculosis
umr05160
Hepatitis C
umr05161
Hepatitis B
umr05162
Measles
umr05163
Human cytomegalovirus infection
umr05164
Influenza A
umr05167
Kaposi sarcoma-associated herpesvirus infection
umr05168
Herpes simplex virus 1 infection
umr05169
Epstein-Barr virus infection
umr05170
Human immunodeficiency virus 1 infection
umr05200
Pathways in cancer
umr05210
Colorectal cancer
umr05222
Small cell lung cancer
umr05416
Viral myocarditis
umr05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
umr00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
103658902
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
103658902
04215 Apoptosis - multiple species
103658902
04115 p53 signaling pathway
103658902
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
103658902
09162 Cancer: specific types
05210 Colorectal cancer
103658902
05222 Small cell lung cancer
103658902
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
103658902
05161 Hepatitis B
103658902
05160 Hepatitis C
103658902
05164 Influenza A
103658902
05162 Measles
103658902
05168 Herpes simplex virus 1 infection
103658902
05163 Human cytomegalovirus infection
103658902
05167 Kaposi sarcoma-associated herpesvirus infection
103658902
05169 Epstein-Barr virus infection
103658902
09171 Infectious disease: bacterial
05132 Salmonella infection
103658902
05134 Legionellosis
103658902
05152 Tuberculosis
103658902
09174 Infectious disease: parasitic
05145 Toxoplasmosis
103658902
09164 Neurodegenerative disease
05010 Alzheimer disease
103658902
05012 Parkinson disease
103658902
05014 Amyotrophic lateral sclerosis
103658902
05016 Huntington disease
103658902
05017 Spinocerebellar ataxia
103658902
05020 Prion disease
103658902
05022 Pathways of neurodegeneration - multiple diseases
103658902
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
103658902
05416 Viral myocarditis
103658902
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
103658902
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
103658902
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
103658902
NCBI-ProteinID:
XP_008684633
UniProt:
A0A384BPV9
LinkDB
All DBs
Position
Unknown
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKTGERADLIAYLKKATKE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatacc
gtggaaaagggaggcaagcacaagactgggccaaatctccatggtttatttggccgaaag
acaggtcaggcccctggattttcttacacggatgccaacaagaacaaaggcatcacctgg
ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagacaggggaaagagcagacttgatagcttatctcaaa
aaagctactaaggagtaa
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integrated database retrieval system