KEGG   Homo sapiens (human): 27102
Entry
27102             CDS       T01001                                 
Symbol
EIF2AK1, HCR, HRI, LEMSPAD, hHRI
Name
(RefSeq) eukaryotic translation initiation factor 2 alpha kinase 1
  KO
K16194  eukaryotic translation initiation factor 2-alpha kinase 1 [EC:2.7.11.1]
Organism
hsa  Homo sapiens (human)
Pathway
hsa05160  Hepatitis C
hsa05162  Measles
hsa05168  Herpes simplex virus 1 infection
Disease
H02457  Developmental delay, leukoencephalopathy, and neurologic decompensation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    27102 (EIF2AK1)
   05162 Measles
    27102 (EIF2AK1)
   05168 Herpes simplex virus 1 infection
    27102 (EIF2AK1)
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01001 Protein kinases [BR:hsa01001]
    27102 (EIF2AK1)
Enzymes [BR:hsa01000]
 2. Transferases
  2.7  Transferring phosphorus-containing groups
   2.7.11  Protein-serine/threonine kinases
    2.7.11.1  non-specific serine/threonine protein kinase
     27102 (EIF2AK1)
Protein kinases [BR:hsa01001]
 Serine/threonine kinases: Other
  PEK family [OT]
   27102 (EIF2AK1)
SSDB
Motif
Pfam: Pkinase PK_Tyr_Ser-Thr Kdo APH
Other DBs
NCBI-GeneID: 27102
NCBI-ProteinID: NP_055228
OMIM: 613635
HGNC: 24921
Ensembl: ENSG00000086232
UniProt: Q9BQI3
Position
7:complement(6022247..6059175)
AA seq 630 aa
MQGGNSGVRKREEEGDGAGAVAAPPAIDFPAEGPDPEYDESDVPAEIQVLKEPLQQPTFP
FAVANQLLLVSLLEHLSHVHEPNPLRSRQVFKLLCQTFIKMGLLSSFTCSDEFSSLRLHH
NRAITHLMRSAKERVRQDPCEDISRIQKIRSREVALEAQTSRYLNEFEELAILGKGGYGR
VYKVRNKLDGQYYAIKKILIKGATKTVCMKVLREVKVLAGLQHPNIVGYHTAWIEHVHVI
QPRADRAAIELPSLEVLSDQEEDREQCGVKNDESSSSSIIFAEPTPEKEKRFGESDTENQ
NNKSVKYTTNLVIRESGELESTLELQENGLAGLSASSIVEQQLPLRRNSHLEESFTSTEE
SSEENVNFLGQTEAQYHLMLHIQMQLCELSLWDWIVERNKRGREYVDESACPYVMANVAT
KIFQELVEGVFYIHNMGIVHRDLKPRNIFLHGPDQQVKIGDFGLACTDILQKNTDWTNRN
GKRTPTHTSRVGTCLYASPEQLEGSEYDAKSDMYSLGVVLLELFQPFGTEMERAEVLTGL
RTGQLPESLRKRCPVQAKYIQHLTRRNSSQRPSAIQLLQSELFQNSGNVNLTLQMKIIEQ
EKEIAELKKQLNLLSQDKGVRDDGKDGGVG
NT seq 1893 nt   +upstreamnt  +downstreamnt
atgcaggggggcaactccggggtccgcaagcgcgaagaggagggcgacggggctggggct
gtggctgcgccgccggccatcgactttcccgccgagggcccggaccccgaatatgacgaa
tctgatgttccagcagaaatccaggtgttaaaagaacccctacaacagccaaccttccct
tttgcagttgcaaaccaactcttgctggtttctttgctggagcacttgagccacgtgcat
gaaccaaacccacttcgttcaagacaggtgtttaagctactttgccagacgtttatcaaa
atggggctgctgtcttctttcacttgtagtgacgagtttagctcattgagactacatcac
aacagagctattactcacttaatgaggtctgctaaagagagagttcgtcaggatccttgt
gaggatatttctcgtatccagaaaatcagatcaagggaagtagccttggaagcacaaact
tcacgttacttaaatgaatttgaagaacttgccatcttaggaaaaggtggatacggaaga
gtatacaaggtcaggaataaattagatggtcagtattatgcaataaaaaaaatcctgatt
aagggtgcaactaaaacagtttgcatgaaggtcctacgggaagtgaaggtgctggcaggt
cttcagcaccccaatattgttggctatcacaccgcgtggatagaacatgttcatgtgatt
cagccacgagcagacagagctgccattgagttgccatctctggaagtgctctccgaccag
gaagaggacagagagcaatgtggtgttaaaaatgatgaaagtagcagctcatccattatc
tttgctgagcccaccccagaaaaagaaaaacgctttggagaatctgacactgaaaatcag
aataacaagtcggtgaagtacaccaccaatttagtcataagagaatctggtgaacttgag
tcgaccctggagctccaggaaaatggcttggctggtttgtctgccagttcaattgtggaa
cagcagctgccactcaggcgtaattcccacctagaggagagtttcacatccaccgaagaa
tcttccgaagaaaatgtcaactttttgggtcagacagaggcacagtaccacctgatgctg
cacatccagatgcagctgtgtgagctctcgctgtgggattggatagtcgagagaaacaag
cggggccgggagtatgtggacgagtctgcctgtccttatgttatggccaatgttgcaaca
aaaatttttcaagaattggtagaaggtgtgttttacatacataacatgggaattgtgcac
cgagatctgaagccaagaaatatttttcttcatggccctgatcagcaagtaaaaatagga
gactttggtctggcctgcacagacatcctacagaagaacacagactggaccaacagaaac
gggaagagaacaccaacacatacgtccagagtgggtacttgtctgtacgcttcacccgaa
cagttggaaggatctgagtatgatgccaagtcagatatgtacagcttgggtgtggtcctg
ctagagctctttcagccgtttggaacagaaatggagcgagcagaagttctaacaggttta
agaactggtcagttgccggaatccctccgtaaaaggtgtccagtgcaagccaagtatatc
cagcacttaacgagaaggaactcatcgcagagaccatctgccattcagctgctgcagagt
gaacttttccaaaattctggaaatgttaacctcaccctacagatgaagataatagagcaa
gaaaaagaaattgcagaactaaagaagcagctaaacctcctttctcaagacaaaggggtg
agggatgacggaaaggatgggggcgtgggatga

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