RNA polymerase II intronic transcription regulatory region sequence-specific DNA binding / locomotor rhythm / aryl hydrocarbon receptor binding / cellular response to Thyroglobulin triiodothyronine / regulation of lipid metabolic process / regulation of glucose metabolic process / Synthesis of bile acids and bile salts / Synthesis of bile acids and bile salts via 27-hydroxycholesterol / Endogenous sterols / Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol ...RNA polymerase II intronic transcription regulatory region sequence-specific DNA binding / locomotor rhythm / aryl hydrocarbon receptor binding / cellular response to Thyroglobulin triiodothyronine / regulation of lipid metabolic process / regulation of glucose metabolic process / Synthesis of bile acids and bile salts / Synthesis of bile acids and bile salts via 27-hydroxycholesterol / Endogenous sterols / Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol / transcription regulator inhibitor activity / cellular response to hormone stimulus / Recycling of bile acids and salts / positive regulation of adipose tissue development / : / Regulation of lipid metabolism by PPARalpha / peroxisome proliferator activated receptor signaling pathway / regulation of cellular response to insulin stimulus / BMAL1:CLOCK,NPAS2 activates circadian expression / SUMOylation of transcription cofactors / Activation of gene expression by SREBF (SREBP) / response to progesterone / nuclear receptor binding / negative regulation of smoothened signaling pathway / circadian regulation of gene expression / mRNA transcription by RNA polymerase II / Heme signaling / Transcriptional activation of mitochondrial biogenesis / Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 / PPARA activates gene expression / Cytoprotection by HMOX1 / Transcriptional regulation of white adipocyte differentiation / RNA polymerase II transcription regulator complex / : / HATs acetylate histones / MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis / transcription regulator complex / Estrogen-dependent gene expression / transcription coactivator activity / protein dimerization activity / nuclear body / protein domain specific binding / RNA polymerase II cis-regulatory region sequence-specific DNA binding / chromatin binding / regulation of DNA-templated transcription / chromatin / negative regulation of transcription by RNA polymerase II / positive regulation of transcription by RNA polymerase II / protein-containing complex / nucleoplasm / nucleus / cytoplasm 類似検索 - 分子機能
Nuclearreceptorcoactivator2 / NCoA-2 / Class E basic helix-loop-helix protein 75 / bHLHe75 / Transcriptional intermediary factor ...NCoA-2 / Class E basic helix-loop-helix protein 75 / bHLHe75 / Transcriptional intermediary factor 2 / hTIF2 / ACE-GLU-LYS-ASN-ALA-LEU-LEU-ARG-TYR-LEU-LEU-ASP-LYS-ASP-NH2
分子量: 1617.889 Da / 分子数: 13 / 断片: UNP Residues 740-752 / 由来タイプ: 合成 詳細: The sequence is supposed to be (ACE)KENALLRYLLDKD(NH2), but during synthesis of the peptide, the first two residues were swapped. 由来: (合成) Homo sapiens (ヒト) / 参照: UniProt: Q15596
プロトコル: SINGLE WAVELENGTH / 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray
放射波長
波長: 0.9722 Å / 相対比: 1
反射
解像度: 1.82→45.2 Å / Num. obs: 32046 / % possible obs: 97.5 % / 冗長度: 4.1 % / Biso Wilson estimate: 25.4 Å2 / Rmerge(I) obs: 0.05 / Net I/σ(I): 15.1
反射 シェル
解像度: 1.82→1.89 Å / 冗長度: 3.6 % / Rmerge(I) obs: 0.558 / Mean I/σ(I) obs: 3 / % possible all: 93.1
-
解析
ソフトウェア
名称
バージョン
分類
DENZO
データ削減
PHENIX
(phenix.refine: dev_1769)
精密化
Coot
モデル構築
Arcimboldo
位相決定
SADABS
データスケーリング
精密化
構造決定の手法: 分子置換 開始モデル: ideal alpha-helix 解像度: 1.82→45.158 Å / SU ML: 0.18 / 交差検証法: FREE R-VALUE / σ(F): 1.34 / 位相誤差: 23.31 / 立体化学のターゲット値: ML 詳細: The occupancy of the C-terminal two residues was set to 0.5 based on weak electron density and clashes between equivalent residues of different chains if they had full occupancy. The peptide ...詳細: The occupancy of the C-terminal two residues was set to 0.5 based on weak electron density and clashes between equivalent residues of different chains if they had full occupancy. The peptide crystallized was therefore probably a mixture of full-length and C-terminally truncated peptide. It is not known at which stage (synthesis or crystallization at acidic pH) the partial hydrolysis occurred.
Rfactor
反射数
%反射
Selection details
Rfree
0.2176
1605
5.01 %
random
Rwork
0.1849
-
-
-
obs
0.1866
32008
97.42 %
-
溶媒の処理
減衰半径: 0.9 Å / VDWプローブ半径: 1.11 Å / 溶媒モデル: FLAT BULK SOLVENT MODEL