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Protein Page:
TAF172 (human)
p Phosphorylation
a Acetylation
m Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
u Ubiquitination
s Sumoylation
n Neddylation
gl O-GlcNAc
ga O-GalNAc
h Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage

Overview
TAF172 Regulates transcription in association with TATA binding protein (TBP). Removes TBP from the TATA box in an ATP-dependent manner. Associates with TBP to form B-TFIID. Binds DRAP1. Belongs to the SNF2/RAD54 helicase family. Note: This description may include information from UniProtKB.
Protein type: EC 3.6.4.-; EC 3.6.1.-; Helicase; Transcription initiation complex
Cellular Component: nucleus
Molecular Function: DNA binding; helicase activity; transcription factor activity; ATP binding
Biological Process: negative regulation of transcription, DNA-dependent
Reference #:  O14981 (UniProtKB)
Alt. Names/Synonyms: ATP-dependent helicase BTAF1; B-TFIID transcription factor-associated 170 kDa subunit; BTAF1; BTAF1 RNA polymerase II, B-TFIID transcription factor-associated, 170kDa (Mot1 homolog, S. cerevisiae); KIAA0940; MGC138406; MOT1; TAF(II)170; TAF-172; TAF172; TAFII170; TATA-binding protein-associated factor 172; TBP-associated factor 172
Gene Symbols: BTAF1
Molecular weight: 206,887 Da
Basal Isoelectric point: 6.08  Predict pI for various phosphorylation states
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

TAF172

Protein Structure Not Found.


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Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 S91-p QEPTSESsMEDsPTT
0 1 S95-p SESsMEDsPTTERLN
0 3 S224-p KLFAKQRsRDAVETN
0 1 S234 AVETNEKSNDstDGE
0 2 S237-p TNEKSNDstDGEPEE
0 1 T238-p NEKSNDstDGEPEEK
0 1 S257-p ANVVINQsANDsKVL
0 1 S261-p INQsANDsKVLIDNI
0 17 Y415-p GGLLGIKyALAVRQD
0 1 K430-u VINTLLPkVLTRIIE
0 1 S925 KIIKNLCSSLCVDPY
0 1 S926 IIKNLCSSLCVDPYL
0 3 Y974-p HRGIITLyRHQKAAF
0 1 Y1256-p DGKKLENyKIPVPIN
0 2 Y1359-p EYLNPLHyTGPPTER
0 1 Y1400-p FRNIKFNyCILDEGH
0 2 S1472-p YGKPILAsRDARSSS
  mouse

 
S90 KQEPTESSMEDSSTT
S94 TESSMEDSSTTDRLN
S223-p KLFAKQRsRDAVETN
S233-p AVETNEKsNDstDGE
S236-p TNEKsNDstDGEPEE
T237-p NEKsNDstDGEPEEK
T256 ANVVINQTASDSKVL
S260 INQTASDSKVLIDNV
Y414-p GGLLGIKyALAVRQD
K429 VINTLLPKVLTRIIE
S924 KVIKNLCSSLCVDPY
S925 VIKNLCSSLCVDPYL
Y973 HRGIITLYRHQKAAF
Y1255 DGKKLENYKIPVPIN
Y1358 EYLNPLHYTGPPTER
Y1399 FRNIKFNYCILDEGH
S1471 YGKPILASRDARSSS
  rat

 
S97 KQEPTECSMEDSSTT
S101 TECSMEDSSTTDRLN
S230-p KLFAKQRsRDAVETN
S240 AVETNEKSNDSTDGE
S243 TNEKSNDSTDGEPEE
T244 NEKSNDSTDGEPEEK
T263 ANVVINQTASDAKVL
A267 INQTASDAKVLIDNV
Y421-p GGLLGIKyALAVRQD
K436 VINTLLPKVLTRIIE
S931-p KVIKNLCssLCVDPY
S932-p VIKNLCssLCVDPYL
Y980 HRGIITLYRHQKAAF
Y1262 DGKKLENYKIPVPIN
Y1365 EYLNPLHYTGPPTER
Y1406 FRNIKFNYCILDEGH
S1478 YGKPILASRDARSSS
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