8CLK の概要
エントリーDOI | 10.2210/pdb8clk/pdb |
EMDBエントリー | 16715 |
分子名称 | General transcription factor 3C polypeptide 1, General transcription factor 3C polypeptide 3, General transcription factor 3C polypeptide 5, ... (4 entities in total) |
機能のキーワード | tfiiic, trna gene, b-box promoter, dna recognition, transcription |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 431127.11 |
構造登録者 | Seifert-Davila, W.,Girbig, M.,Hauptmann, L.,Hoffmann, T.,Eustermann, S.,Mueller, C.W. (登録日: 2023-02-16, 公開日: 2023-06-21, 最終更新日: 2025-07-09) |
主引用文献 | Seifert-Davila, W.,Girbig, M.,Hauptmann, L.,Hoffmann, T.,Eustermann, S.,Muller, C.W. Structural insights into human TFIIIC promoter recognition. Sci Adv, 9:eadh2019-eadh2019, 2023 Cited by PubMed Abstract: Transcription factor (TF) IIIC recruits RNA polymerase (Pol) III to most of its target genes. Recognition of intragenic A- and B-box motifs in transfer RNA (tRNA) genes by TFIIIC modules τA and τB is the first critical step for tRNA synthesis but is mechanistically poorly understood. Here, we report cryo-electron microscopy structures of the six-subunit human TFIIIC complex unbound and bound to a tRNA gene. The τB module recognizes the B-box via DNA shape and sequence readout through the assembly of multiple winged-helix domains. TFIIIC220 forms an integral part of both τA and τB connecting the two subcomplexes via a ~550-amino acid residue flexible linker. Our data provide a structural mechanism by which high-affinity B-box recognition anchors TFIIIC to promoter DNA and permits scanning for low-affinity A-boxes and TFIIIB for Pol III activation. PubMed: 37418517DOI: 10.1126/sciadv.adh2019 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.5 Å) |
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