6wfk

Crystal structure of human Naa50 in complex with CoA and an inhibitor (compound 4a) identified using DNA encoded library technology

Method: X-RAY DIFFRACTION Dmax: 109.4 Å Quality: GOOD

1. 蛋白身份与相关结构 Protein Identity & Related Structures

N-alpha-acetyltransferase 50

Homo sapiens

UniProt Q9GZZ1

当前结构中的状态

Assembly 聚集状态 构建体 突变与修饰 配体、离子与共同组分 实验方法与环境 结构质量
1 蛋白单体 单体 蛋白 × 1 PDB 声明:monomeric(1) 与蛋白拷贝数一致 链 A; UniProt 1–169 未记录 COA COENZYME A × 1 U2J (4S)-1-methyl-N-{(3S,5S)-5-[4-(methylcarbamoyl)-1,3-thiazol-2-yl]-1-[4-(1H-tetrazol-5-yl)benzene-1-carbonyl]pyrrolidin-3-yl}-2,6-dioxohexahydropyrimidine-4-carboxamide × 1 X-RAY DIFFRACTION X-ray结晶条件:VAPOR DIFFUSION, SITTING DROP;pH 5;294 K;Compound 4a soaked into crystals of Naa50+CoA. CoA co-crystals: Naa50 apo protein (14.3 mg/ml) was incubated with CoA in a 1:3 molar ratio on ice for 60 min. Crystallization solution: 0.1 M Na acetate, pH5.0, 25% (w/v) PEG 3350, 10 mM Dithiothreitol (DTT), and 0.1% Dioxane 分辨率 1.87 Å R-free 0.222
2 蛋白单体 单体 蛋白 × 1 PDB 声明:monomeric(1) 与蛋白拷贝数一致 链 B; UniProt 1–169 未记录 COA COENZYME A × 1 U2J (4S)-1-methyl-N-{(3S,5S)-5-[4-(methylcarbamoyl)-1,3-thiazol-2-yl]-1-[4-(1H-tetrazol-5-yl)benzene-1-carbonyl]pyrrolidin-3-yl}-2,6-dioxohexahydropyrimidine-4-carboxamide × 1 X-RAY DIFFRACTION X-ray结晶条件:VAPOR DIFFUSION, SITTING DROP;pH 5;294 K;Compound 4a soaked into crystals of Naa50+CoA. CoA co-crystals: Naa50 apo protein (14.3 mg/ml) was incubated with CoA in a 1:3 molar ratio on ice for 60 min. Crystallization solution: 0.1 M Na acetate, pH5.0, 25% (w/v) PEG 3350, 10 mM Dithiothreitol (DTT), and 0.1% Dioxane 分辨率 1.87 Å R-free 0.222
3 蛋白单体 单体 蛋白 × 1 PDB 声明:monomeric(1) 与蛋白拷贝数一致 链 C; UniProt 1–169 未记录 COA COENZYME A × 1 U2J (4S)-1-methyl-N-{(3S,5S)-5-[4-(methylcarbamoyl)-1,3-thiazol-2-yl]-1-[4-(1H-tetrazol-5-yl)benzene-1-carbonyl]pyrrolidin-3-yl}-2,6-dioxohexahydropyrimidine-4-carboxamide × 1 X-RAY DIFFRACTION X-ray结晶条件:VAPOR DIFFUSION, SITTING DROP;pH 5;294 K;Compound 4a soaked into crystals of Naa50+CoA. CoA co-crystals: Naa50 apo protein (14.3 mg/ml) was incubated with CoA in a 1:3 molar ratio on ice for 60 min. Crystallization solution: 0.1 M Na acetate, pH5.0, 25% (w/v) PEG 3350, 10 mM Dithiothreitol (DTT), and 0.1% Dioxane 分辨率 1.87 Å R-free 0.222

数据库中的同蛋白其他状态

以下每一行都是同一 UniProt 蛋白在另一个 PDB 条目中的 biological assembly, “相对当前条目”直接指出证据层面的不同;没有差异标签表示当前已读取字段一致。

共 14 个其他 PDB 条目、30 个 assembly。 打开独立比较页并筛选聚集状态

查看构建体与数据证据
UniProt名称 NAA50_HUMAN
Isoform
PDB实体 1
链与序列区间 作者链 A; PDB构建体 3–171; UniProt 1–169 作者链 B; PDB构建体 3–171; UniProt 1–169 作者链 C; PDB构建体 3–171; UniProt 1–169

页面优先展示蛋白身份、当前 assembly、共同组分、聚集状态和跨 PDB 结构链接。 链映射与序列区间收在“数据证据”中;数据库内部编号、导入时间和 assembly 操作表达式仅用于维护,因此不在读者页面展示。

SAXS 散射曲线 SAXS Profile

SAXS profile for 6wfk

P(r) 距离分布 P(r) Distribution

P(r) distribution for 6wfk
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2. 结构基本信息 2. Structure Basics

条目编号 entry_id6wfk
沉积日期 deposition_date2020-04-03
结构标题 titleCrystal structure of human Naa50 in complex with CoA and an inhibitor (compound 4a) identified using DNA encoded library technology
关键词 keywordsN-alpha-acetyltransferase 50, Inhibitor complex, DNA encoded library, CoA, TRANSFERASE; TRANSFERASE
实验方法 methodX-RAY DIFFRACTION

3. SAXS 参数 (CRYSOL 理论计算) 3. SAXS Parameters (CRYSOL)

回转半径 Rg (Guinier) rg_guinier31.48
回转半径 Rg (电子) rg_electron31.55
零角强度 I(0) i052716100.00
分子量 molecular_weight56444.0 kDa
排除体积 excluded_volume70333 ų
包络体积 envelope_volume88856 ų
水化壳体积 shell_volume26235 ų
包络直径 envelope_diameter116.5
壳层 Rg shell_rg34.69
包络 Rg envelope_rg31.53
形状 Rg shape_rg31.59
总 Rg total_rg31.70
总原子数 total_atoms4028
残基数 n_residues456
球谐函数阶数 n_harmonics20
q 范围 q_range— – 0.5000 −1
数据点数 n_points101
壳层类型 shell_typedirectional
溶剂电子密度 solvent_density0.3340 e/ų
壳层衬度 contrast_shell0.0300 e/ų
CRYSOL 版本 crysol_version4.1.3

4. P(r) 距离分布 (GNOM 反演) 4. P(r) Analysis (GNOM)

最大尺寸 Dmax dmax109.4
Rg (实空间) rg_real31.96
Rg 误差 (实空间) rg_real_error0.97
I(0) (实空间) i0_real5.2720e+07
I(0) 误差 (实空间) i0_real_error8.4880e+05
Rg (倒空间) rg_reciprocal31.76
I(0) (倒空间) i0_reciprocal52710000.0000
解质量估计 total_estimate0.7807
解质量评级 solution_quality GOOD a GOOD solution
P(r) 峰数 n_peaks1
主峰位置 r_peak_primary26.3
偏度 Skewness skewness0.594
峰度 Kurtosis kurtosis-0.374
角度范围 angular_range— – 0.2500 −1
当前正则化参数 α current_alpha0.0000
最高正则化参数 α highest_alpha18090000.0000
实空间数据点数 n_real_points51
GNOM 版本 gnom_version4.1.3
质量判据 quality_criteria AN1: 0.000; Oscil: 0.592; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.552; Smooth: 0.817

5. 晶体学与实验 5. Crystallography & Experiment

6. 实体与聚合物信息 Entities & Polymers (4)

7. 折叠分类 (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

结构域编号 domain_idd6wfka_
类 Class classd — Alpha and beta proteins (a+b)
折叠类型 Fold foldd.108 — Acyl-CoA N-acyltransferases (Nat)
超家族 Superfamily superfamilyd.108.1 — Acyl-CoA N-acyltransferases (Nat)
家族 Family familyd.108.1.0 — automated matches
结构域编号 domain_idd6wfkb_
类 Class classd — Alpha and beta proteins (a+b)
折叠类型 Fold foldd.108 — Acyl-CoA N-acyltransferases (Nat)
超家族 Superfamily superfamilyd.108.1 — Acyl-CoA N-acyltransferases (Nat)
家族 Family familyd.108.1.0 — automated matches
结构域编号 domain_idd6wfkc_
类 Class classd — Alpha and beta proteins (a+b)
折叠类型 Fold foldd.108 — Acyl-CoA N-acyltransferases (Nat)
超家族 Superfamily superfamilyd.108.1 — Acyl-CoA N-acyltransferases (Nat)
家族 Family familyd.108.1.0 — automated matches

CATH v4.4 (3 domains)

结构域编号 domain_id6wfkA00
类 Class class3 — Alpha Beta
架构 Architecture architecture40 — 3-Layer(aba) Sandwich
拓扑 Topology topology630 — Aminopeptidase
同源超家族 H-superfamily homologous superfamily30 — Gcn5-related N-acetyltransferase (GNAT)
结构域编号 domain_id6wfkB00
类 Class class3 — Alpha Beta
架构 Architecture architecture40 — 3-Layer(aba) Sandwich
拓扑 Topology topology630 — Aminopeptidase
同源超家族 H-superfamily homologous superfamily30 — Gcn5-related N-acetyltransferase (GNAT)
结构域编号 domain_id6wfkC00
类 Class class3 — Alpha Beta
架构 Architecture architecture40 — 3-Layer(aba) Sandwich
拓扑 Topology topology630 — Aminopeptidase
同源超家族 H-superfamily homologous superfamily30 — Gcn5-related N-acetyltransferase (GNAT)

8. 引用文献 (1)

9. 文件与曲线 (10)