KEGG   Homo sapiens (human): 6908
Entry
6908              CDS       T01001                                 
Symbol
TBP, GTF2D, GTF2D1, HDL4, SCA17, TBP1, TFIID
Name
(RefSeq) TATA-box binding protein
  KO
K03120  transcription initiation factor TFIID TATA-box-binding protein
Organism
hsa  Homo sapiens (human)
Pathway
hsa03022  Basal transcription factors
hsa05016  Huntington disease
hsa05017  Spinocerebellar ataxia
hsa05165  Human papillomavirus infection
hsa05166  Human T-cell leukemia virus 1 infection
hsa05203  Viral carcinogenesis
Network
nt06166  Human papillomavirus (HPV)
  Element
N00376  HPV E7 to TBP1-mediated transcription
Disease
H00063  Spinocerebellar ataxia (SCA)
H01243  Huntington disease-like syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09121 Transcription
   03022 Basal transcription factors
    6908 (TBP)
 09160 Human Diseases
  09161 Cancer: overview
   05203 Viral carcinogenesis
    6908 (TBP)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    6908 (TBP)
   05165 Human papillomavirus infection
    6908 (TBP)
  09164 Neurodegenerative disease
   05016 Huntington disease
    6908 (TBP)
   05017 Spinocerebellar ataxia
    6908 (TBP)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    6908 (TBP)
   03021 Transcription machinery [BR:hsa03021]
    6908 (TBP)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  beta-Scaffold factors with minor groove contacts
   TATA-binding proteins
    6908 (TBP)
Transcription machinery [BR:hsa03021]
 Eukaryotic type
  RNA polymerase II system
   Basal transcription factors
    TFIID
     6908 (TBP)
  RNA polymerase III system
    TFIIIB
     6908 (TBP)
  RNA polymerase I system
    SL1/TIF-1B
     6908 (TBP)
SSDB
Motif
Pfam: TBP DDHD EPL1 Peptidase_S64 TFIIA DUF4746 TMEM51 Tra1_central Cellulose_synt PAT1 MDM10 DUF1501 Tim54 Presenilin SpoIIP FemAB
Other DBs
NCBI-GeneID: 6908
NCBI-ProteinID: NP_003185
OMIM: 600075
HGNC: 11588
Ensembl: ENSG00000112592
UniProt: P20226 Q32MN7
Structure
Position
6:170554369..170572859
AA seq 339 aa
MDQNNSLPPYAQGLASPQGAMTPGIPIFSPMMPYGTGLTPQPIQNTNSLSILEEQQRQQQ
QQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQAVAAAAVQQSTSQQATQGTSGQAPQ
LFHSQTLTTAPLPGTTPLYPSPMTPMTPITPATPASESSGIVPQLQNIVSTVNLGCKLDL
KTIALRARNAEYNPKRFAAVIMRIREPRTTALIFSSGKMVCTGAKSEEQSRLAARKYARV
VQKLGFPAKFLDFKIQNMVGSCDVKFPIRLEGLVLTHQQFSSYEPELFPGLIYRMIKPRI
VLLIFVSGKVVLTGAKVRAEIYEAFENIYPILKGFRKTT
NT seq 1020 nt   +upstreamnt  +downstreamnt
atggatcagaacaacagcctgccaccttacgctcagggcttggcctcccctcagggtgcc
atgactcccggaatccctatctttagtccaatgatgccttatggcactggactgacccca
cagcctattcagaacaccaatagtctgtctattttggaagagcaacaaaggcagcagcag
caacaacaacagcagcagcagcagcagcagcagcaacagcaacagcagcagcagcagcag
cagcagcagcagcagcagcagcagcagcagcagcagcagcaacaggcagtggcagctgca
gccgttcagcagtcaacgtcccagcaggcaacacagggaacctcaggccaggcaccacag
ctcttccactcacagactctcacaactgcacccttgccgggcaccactccactgtatccc
tcccccatgactcccatgacccccatcactcctgccacgccagcttcggagagttctggg
attgtaccgcagctgcaaaatattgtatccacagtgaatcttggttgtaaacttgaccta
aagaccattgcacttcgtgcccgaaacgccgaatataatcccaagcggtttgctgcggta
atcatgaggataagagagccacgaaccacggcactgattttcagttctgggaaaatggtg
tgcacaggagccaagagtgaagaacagtccagactggcagcaagaaaatatgctagagtt
gtacagaagttgggttttccagctaagttcttggacttcaagattcagaatatggtgggg
agctgtgatgtgaagtttcctataaggttagaaggccttgtgctcacccaccaacaattt
agtagttatgagccagagttatttcctggtttaatctacagaatgatcaaacccagaatt
gttctccttatttttgtttctggaaaagttgtattaacaggtgctaaagtcagagcagaa
atttatgaagcatttgaaaacatctaccctattctaaagggattcaggaagacgacgtaa

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