IgG binding / error-prone translesion synthesis / translesion synthesis / Translesion synthesis by POLI / Termination of translesion DNA synthesis / cytoplasmic ribonucleoprotein granule / damaged DNA binding / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / DNA replication ...IgG binding / error-prone translesion synthesis / translesion synthesis / Translesion synthesis by POLI / Termination of translesion DNA synthesis / cytoplasmic ribonucleoprotein granule / damaged DNA binding / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / DNA replication / nuclear speck / DNA repair / extracellular region / nucleoplasm / metal ion binding 類似検索 - 分子機能
HUWE1/Rev1, ubiquitin binding region / Ubiquitin binding region / : / DNA polymerase-iota, thumb domain / IgG-binding B / B domain / M protein-type anchor domain / GA-like domain / GA-like domain / Immunoglobulin/albumin-binding domain superfamily ...HUWE1/Rev1, ubiquitin binding region / Ubiquitin binding region / : / DNA polymerase-iota, thumb domain / IgG-binding B / B domain / M protein-type anchor domain / GA-like domain / GA-like domain / Immunoglobulin/albumin-binding domain superfamily / YSIRK Gram-positive signal peptide / DNA polymerase, Y-family, little finger domain / impB/mucB/samB family C-terminal domain / UmuC domain / DNA polymerase, Y-family, little finger domain superfamily / impB/mucB/samB family / UmuC domain profile. / LPXTG cell wall anchor motif / Gram-positive cocci surface proteins LPxTG motif profile. / LPXTG cell wall anchor domain / Reverse transcriptase/Diguanylate cyclase domain / DNA/RNA polymerase superfamily 類似検索 - ドメイン・相同性
Immunoglobulin G-binding protein G / DNA polymerase iota 類似検索 - 構成要素
ACCORDING TO THE AUTHORS THE N-TERMINAL PART IS A GB1 TAG USED FOR ENHANCEMENT OF PROTEIN ...ACCORDING TO THE AUTHORS THE N-TERMINAL PART IS A GB1 TAG USED FOR ENHANCEMENT OF PROTEIN SOLUBILITY. THEY CHOOSE TO DEPOSIT ONLY THE C-TERMINAL PART OF THE SEQUENCE CORRESPONDING TO DNA POLYMERASE IOTA. THESE 2 SEGMENTS ARE LINKED BY THE RESIDUES GSDE
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実験情報
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実験
実験
手法: 溶液NMR 詳細: Solution Structure of the Ubiquitin-Binding Motif of Human Polymerase Iota
NMR実験
Conditions-ID
Experiment-ID
Solution-ID
タイプ
1
1
1
3D (H)CCH-TOCSY
1
2
1
3D HNCA
1
3
1
3D HN(CA)CB
1
4
1
3DHN(CO)CA
1
5
1
3D HNCO
1
6
1
3DHN(COCA)CB
1
7
1
3D 1H-15N NOESY
1
8
1
3D 1H-13C NOESY
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試料調製
詳細
内容: 1-4 mM [U-100% 13C; U-100% 15N] D2O-1, 1-4 mM [U-100% 13C; U-100% 15N] H2O-2, 100% D2O 溶媒系: 100% D2O
試料
単位
構成要素
Isotopic labeling
Conc. range (mg/ml)
Solution-ID
mM
D2O-1
[U-100% 13C; U-100% 15N]
1-4
1
mM
H2O-2
[U-100% 13C; U-100% 15N]
1-4
1
試料状態
イオン強度: 0.1 / pH: 7 / 圧: ambient / 温度: 25 K
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NMR測定
NMRスペクトロメーター
タイプ
製造業者
モデル
磁場強度 (MHz)
Spectrometer-ID
Varian INOVA
Varian
INOVA
800
1
Varian INOVA
Varian
INOVA
600
2
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解析
NMR software
名称
バージョン
開発者
分類
X-PLOR NIH
2.19
Schwieters, Kuszewski, TjandraandClore
構造決定
X-PLOR NIH
2.19
Schwieters, Kuszewski, TjandraandClore
精密化
精密化
手法: simulated annealing / ソフトェア番号: 1
代表構造
選択基準: lowest energy
NMRアンサンブル
コンフォーマー選択の基準: structures with the lowest energy 計算したコンフォーマーの数: 40 / 登録したコンフォーマーの数: 25