Homo sapiens (human): 1965
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Entry
1965 CDS
T01001
Symbol
EIF2S1, EIF-2, EIF-2A, EIF-2alpha, EIF2, EIF2A
Name
(RefSeq) eukaryotic translation initiation factor 2 subunit alpha
KO
K03237
translation initiation factor 2 subunit 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04137
Mitophagy - animal
hsa04140
Autophagy - animal
hsa04141
Protein processing in endoplasmic reticulum
hsa04210
Apoptosis
hsa04932
Non-alcoholic fatty liver disease
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05160
Hepatitis C
hsa05162
Measles
hsa05164
Influenza A
hsa05168
Herpes simplex virus 1 infection
hsa05417
Lipid and atherosclerosis
Network
nt06168
Herpes simplex virus 1 (HSV-1)
nt06169
Measles virus (MV)
nt06170
Influenza A virus (IAV)
nt06460
Alzheimer disease
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06465
Prion disease
nt06466
Pathways of neurodegeneration
nt06534
Unfolded protein response
Element
N00571
PKR-eIF2alpha signaling pathway
N00572
HSV ICP34.5 to PKR-eIF2alpha signaling pathway
N01009
PERK-ATF4 signaling pathway
N01010
Mutation-caused aberrant PSEN1 to PERK-ATF4 signaling pathway
N01035
Mutation-caused aberrant SNCA to PERK-ATF4 signaling pathway
N01149
Mutation-caused aberrant SOD1 to PERK-ATF4 signaling pathway
N01198
Scrapie conformation PrPSc to PERK-ATF4 signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
04141 Protein processing in endoplasmic reticulum
1965 (EIF2S1)
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
1965 (EIF2S1)
04137 Mitophagy - animal
1965 (EIF2S1)
09143 Cell growth and death
04210 Apoptosis
1965 (EIF2S1)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
1965 (EIF2S1)
05164 Influenza A
1965 (EIF2S1)
05162 Measles
1965 (EIF2S1)
05168 Herpes simplex virus 1 infection
1965 (EIF2S1)
09164 Neurodegenerative disease
05010 Alzheimer disease
1965 (EIF2S1)
05012 Parkinson disease
1965 (EIF2S1)
05014 Amyotrophic lateral sclerosis
1965 (EIF2S1)
05020 Prion disease
1965 (EIF2S1)
05022 Pathways of neurodegeneration - multiple diseases
1965 (EIF2S1)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
1965 (EIF2S1)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
1965 (EIF2S1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03012 Translation factors [BR:
hsa03012
]
1965 (EIF2S1)
Translation factors [BR:
hsa03012
]
Eukaryotic type
Initiation factors
eIF-2
1965 (EIF2S1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EIF_2_alpha
S1
Motif
Other DBs
NCBI-GeneID:
1965
NCBI-ProteinID:
NP_004085
OMIM:
603907
HGNC:
3265
Ensembl:
ENSG00000134001
UniProt:
P05198
Q53XC0
Structure
PDB
PDBj
LinkDB
All DBs
Position
14:67360328..67386516
Genome browser
AA seq
315 aa
AA seq
DB search
MPGLSCRFYQHKFPEVEDVVMVNVRSIAEMGAYVSLLEYNNIEGMILLSELSRRRIRSIN
KLIRIGRNECVVVIRVDKEKGYIDLSKRRVSPEEAIKCEDKFTKSKTVYSILRHVAEVLE
YTKDEQLESLFQRTAWVFDDKYKRPGYGAYDAFKHAVSDPSILDSLDLNEDEREVLINNI
NRRLTPQAVKIRADIEVACYGYEGIDAVKEALRAGLNCSTENMPIKINLIAPPRYVMTTT
TLERTEGLSVLSQAMAVIKEKIEEKRGVFNVQMEPKVVTDTDETELARQMERLERENAEV
DGDDDAEEMEAKAED
NT seq
948 nt
NT seq
+upstream
nt +downstream
nt
atgccgggtctaagttgtagattttatcaacacaaatttcctgaggtggaagatgtagtg
atggtgaatgtcagatccattgctgaaatgggggcttatgtcagcttgctggaatacaac
aacattgaaggcatgattcttcttagtgaattatccagaaggcgtatccgttctatcaac
aaactcatccgaattggcaggaatgagtgtgtggttgtcattagggtggacaaagaaaaa
ggatatattgatttgtcaaaaagaagagtttctccagaggaagcaatcaaatgtgaagac
aaattcacaaaatccaaaactgtttatagcattcttcgtcatgttgctgaggtgttagaa
tacaccaaggatgagcagctggaaagcctattccagaggactgcctgggtctttgatgac
aagtacaagagacctggatatggtgcctatgatgcatttaagcatgcagtctcagaccca
tctattttggatagtttagatttgaatgaagatgaacgggaagtactcattaataatatt
aataggcgcttgaccccacaggctgtcaaaattcgagcagatattgaagtggcttgttat
ggttatgaaggcattgatgctgtaaaagaagccctaagagcaggtttgaattgttctaca
gaaaacatgcccattaagattaatctaatagctcctcctcggtatgtaatgactacgaca
accctggagagaacagaaggcctttctgtcctcagtcaagctatggctgttatcaaagag
aagattgaggaaaagaggggtgtgttcaatgttcaaatggagcccaaagtggtcacagat
acagatgagactgaacttgcgaggcagatggagaggcttgaaagagaaaatgccgaagtg
gatggagatgatgatgcagaagaaatggaagccaaagctgaagattaa
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