Homo sapiens (human): 10629
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Entry
10629 CDS
T01001
Symbol
TAF6L, PAF65A
Name
(RefSeq) TATA-box binding protein associated factor 6 like
KO
K03131
transcription initiation factor TFIID subunit 6
Organism
hsa
Homo sapiens (human)
Pathway
hsa03022
Basal transcription factors
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09121 Transcription
03022 Basal transcription factors
10629 (TAF6L)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03021 Transcription machinery [BR:
hsa03021
]
10629 (TAF6L)
03036 Chromosome and associated proteins [BR:
hsa03036
]
10629 (TAF6L)
Transcription machinery [BR:
hsa03021
]
Eukaryotic type
RNA polymerase II system
Basal transcription factors
TFIID
10629 (TAF6L)
Coactivators
SAGA/TFTC/STAGA complex
10629 (TAF6L)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
HAT complexes
PCAF complex
10629 (TAF6L)
STAGA complex
10629 (TAF6L)
TFTC complex
10629 (TAF6L)
SAGA complex
10629 (TAF6L)
SLIK complex
10629 (TAF6L)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TAF6_C
TAF
Motif
Other DBs
NCBI-GeneID:
10629
NCBI-ProteinID:
NP_006464
OMIM:
602946
HGNC:
17305
Ensembl:
ENSG00000162227
UniProt:
Q9Y6J9
A8K0D4
Structure
PDB
LinkDB
All DBs
Position
11:62771396..62787342
Genome browser
AA seq
622 aa
AA seq
DB search
MSEREERRFVEIPRESVRLMAESTGLELSDEVAALLAEDVCYRLREATQNSSQFMKHTKR
RKLTVEDFNRALRWSSVEAVCGYGSQEALPMRPAREGELYFPEDREVNLVELALATNIPK
GCAETAVRVHVSYLDGKGNLAPQGSVPSAVSSLTDDLLKYYHQVTRAVLGDDPQLMKVAL
QDLQTNSKIGALLPYFVYVVSGVKSVSHDLEQLHRLLQVARSLFRNPHLCLGPYVRCLVG
SVLYCVLEPLAASINPLNDHWTLRDGAALLLSHIFWTHGDLVSGLYQHILLSLQKILADP
VRPLCCHYGAVVGLHALGWKAVERVLYPHLSTYWTNLQAVLDDYSVSNAQVKADGHKVYG
AILVAVERLLKMKAQAAEPNRGGPGGRGCRRLDDLPWDSLLFQESSSGGGAEPSFGSGLP
LPPGGAGPEDPSLSVTLADIYRELYAFFGDSLATRFGTGQPAPTAPRPPGDKKEPAAAPD
SVRKMPQLTASAIVSPHGDESPRGSGGGGPASASGPAASESRPLPRVHRARGAPRQQGPG
TGTRDVFQKSRFAPRGAPHFRFIIAGRQAGRRCRGRLFQTAFPAPYGPSPASRYVQKLPM
IGRTSRPARRWALSDYSLYLPL
NT seq
1869 nt
NT seq
+upstream
nt +downstream
nt
atgtcagagcgagaagagcggcggtttgtggagatccctcgggagtctgtccggctcatg
gcggagagcacgggcctggagctgagcgatgaggtggcggcgctgctcgcagaggacgtg
tgctatcgtctgagagaggccacgcagaatagctctcagttcatgaagcacaccaaacgc
cggaagctgacggttgaggacttcaacagggccctcagatggagcagcgtggaggctgtg
tgtggttacggatcacaggaggcactgcccatgcgccccgccagggagggtgaactctac
tttcctgaggatcgagaggtgaacctggtggagctggccctggctaccaacatccccaaa
ggctgtgctgagacagctgtcagagttcatgtctcctacctggatggcaaagggaacctg
gcacctcaaggatcggtgcccagtgctgtgtcttcactgacagatgaccttctcaagtac
tatcaccaggtgactcgtgctgtgctaggggatgatccgcaactgatgaaggttgcactc
caggacttgcagacgaactccaagattggggcactcctgccttactttgtttatgtggtc
agtggggtgaaatctgtaagccatgacctggagcaactgcaccggctgctgcaggtggca
cggagcctatttcgtaatccgcacctgtgcttggggccctatgtccgctgtctggtgggc
agtgtcctctactgtgtcctggagccactggctgcctccatcaaccccctgaatgaccac
tggactctgcgggatggggctgccctcctgctcagccacatcttctggactcatggggac
cttgtaagtggcctctatcagcatatcctgctatccctgcagaagatcctggcagatcct
gtgcggccgctctgctgccactatggagccgtggtggggctgcatgctcttggctggaag
gcagtagaacgagtcctgtacccacacctgtccacctactggacaaacttgcaggctgtg
ctggatgattattcagtatctaatgcccaggtcaaagcagatggacacaaagtctatgga
gccattctggtggcggtagagcgactgctgaagatgaaggcccaggcagcagagcccaac
aggggtggcccaggtggcagggggtgccggcgcctggacgacctgccatgggacagcctt
ctctttcaagagtcgtcctccgggggcggtgcagaacccagctttgggtccggcctcccg
ctgccgccagggggcgcggggccggaggacccttctctttcggtgaccctggccgacatc
taccgggagctctacgccttcttcggtgacagcttggccacacgctttggcaccggccag
cctgcacccacggctccgcggccgcccggggacaagaaggagccggcggcagccccggac
tcggtgcggaagatgccgcagctgacggcaagcgccatagtcagcccgcacggcgacgag
agcccccggggcagcggcggaggcggccccgcgtcggcctctgggcccgccgcctctgag
agcaggcccttgccgcgcgtgcatcgggcgcgcggggcaccccggcagcagggccccggg
accggcacccgcgacgttttccagaagagccgtttcgccccgcgcggcgccccgcacttt
cgtttcatcatagccgggcggcaggctgggaggcgctgccgcgggcgccttttccagact
gccttccccgcgccgtacgggcctagcccggcctcgcgctacgtgcagaaactgcccatg
atcggccgtaccagccgccccgcccgccggtgggcgctctcggactactcgctgtacttg
ccgctctga
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