KEGG   Homo sapiens (human): 2874
Entry
2874              CDS       T01001                                 
Symbol
GPS2, AMF-1
Name
(RefSeq) G protein pathway suppressor 2
  KO
K15307  G protein pathway suppressor 2
Organism
hsa  Homo sapiens (human)
Pathway
hsa05166  Human T-cell leukemia virus 1 infection
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    2874 (GPS2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    2874 (GPS2)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Histone modification proteins
   HDAC complexes
    SMART complex
     2874 (GPS2)
SSDB
Motif
Pfam: G_path_suppress MAT1 DUF2252
Other DBs
NCBI-GeneID: 2874
NCBI-ProteinID: NP_004480
OMIM: 601935
HGNC: 4550
Ensembl: ENSG00000132522
UniProt: Q13227
Structure
Position
17:complement(7312661..7315360)
AA seq 327 aa
MPALLERPKLSNAMARALHRHIMMERERKRQEEEEVDKMMEQKMKEEQERRKKKEMEERM
SLEETKEQILKLEEKLLALQEEKHQLFLQLKKVLHEEEKRRRKEQSDLTTLTSAAYQQSL
TVHTGTHLLSMQGSPGGHNRPGTLMAADRAKQMFGPQVLTTRHYVGSAAAFAGTPEHGQF
QGSPGGAYGTAQPPPHYGPTQPAYSPSQQLRAPSAFPAVQYLSQPQPQPYAVHGHFQPTQ
TGFLQPGGALSLQKQMEHANQQTGFSDSSSLRPMHPQALHPAPGLLASPQLPVQMQPAGK
SGFAATSQPGPRLPFIQHSQNPRFYHK
NT seq 984 nt   +upstreamnt  +downstreamnt
atgcccgcactcctggagcgccccaagctttccaacgccatggccagggcgctgcaccgg
cacattatgatggagcgggagcgcaagcggcaggaggaagaagaggtggataagatgatg
gaacagaagatgaaggaagaacaggagagaaggaagaaaaaggagatggaagagagaatg
tcattagaggagaccaaggaacaaattctgaagttggaggagaagcttttggctctacag
gaagagaagcaccagcttttcctgcagctcaagaaagttttacatgaggaagaaaaacgg
aggcgaaaggaacagagtgacctgaccaccctaacatcagctgcataccagcagagcctg
actgttcacacaggaactcatctcctcagcatgcaggggagccctggaggacacaatcgc
ccaggcaccctcatggcagctgacagagccaaacaaatgtttggaccccaagtgcttacg
acccggcactacgtgggctcagcagctgcttttgcagggacaccagagcatggacaattc
caaggcagtcctggtggtgcctatgggactgctcagcccccacctcactatgggcccaca
cagccagcttatagtcctagtcagcagctcagagctccttcggcattccctgcagtgcag
tacctatctcagccacagccacagccctatgctgtgcatggccactttcagcccactcag
acaggtttcctccagcctggtggtgccctgtccttgcaaaagcagatggaacatgctaac
cagcagactggcttctccgactcatcctctctgcgccccatgcacccccaggctctgcat
ccagcccctggactccttgcttccccccagctccctgtgcagatgcagccagcaggaaag
tcgggctttgcagctaccagccaacctggccctcggctccccttcatccaacacagccag
aacccgcgattctaccacaagtga

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