SRCAP (Homo sapiens)
AT hook

TF Information

Pfam ID Interpro ID Gene ID CIS-BP ID Sequence source Animal TF db
PF02178 (AT_hook) IPR017956 ENSG00000080603 T017387_2.00 Ensembl (2018-Dec-8) Link out
NCBI Gene Info:
This gene encodes the core catalytic component of the multiprotein chromatin-remodeling SRCAP complex. The encoded protein is an ATPase that is necessary for the incorporation of the histone variant H2A.Z into nucleosomes. It can function as a transcriptional activator in Notch-mediated, CREB-mediated and steroid receptor-mediated transcription. Mutations in this gene cause Floating-Harbor syndrome, a rare disorder characterized by short stature, language deficits and dysmorphic facial features. [provided by RefSeq, Feb 2012]

Directly determined binding motifs

Name/Motif ID Species Forward Reverse Type/Study/Study ID SR
Score
DBD
Identity
No direct experiments

Motifs from related TFs

Name/Motif ID Species Forward Reverse Type/Study/Study ID SR
Score
DBD
Identity
No TFs with similar DNA binding domains

DNA Binding Domains

Protein ID Domain From To Sequence
ENSP00000262518 AT hook 2856 2868
ENSP00000262518 AT hook 2935 2947
ENSP00000262518 AT hook 3003 3015
ENSP00000378499 AT hook 2597 2609
ENSP00000378499 AT hook 2676 2688
ENSP00000378499 AT hook 2744 2756

Links

Other AT hook family TFs
Other Homo sapiens TFs

0 Related TFs

">No related TF found