2mow

Structure of Nrd1p CID - Trf4p NIM complex

Method: SOLUTION NMR Dmax: 65.8 Å Quality: REASONABLE

1. Protein Identity and Related Structures Protein Identity & Related Structures

Protein NRD1

Saccharomyces cerevisiae

UniProt P53617

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–153 Fragment:CID (UNP residues 1-153) Poly(A) RNA polymerase protein 2 × 1 (P53632) SOLUTION NMR NMR measurement conditions:pH 8;293.15 K;Ionic strength (raw mmCIF value) 0.1;Pressure ambient NMR sample composition:1.5 mM Trf4p, 1 mM [U-99% 13C; U-99% 15N] Nrd1p, 100 mM sodium chloride, 50 mM sodium phosphate, 90% H2O/10% D2O | 90% H2O/10% D2O Resolution not provided

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

13 other PDB entries and 18 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NRD1_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–153; UniProt 1–153

Poly(A) RNA polymerase protein 2

OrganismNot specified

UniProt P53632

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 573–584 Fragment:NIM (UNP residues 573-584) Protein NRD1 × 1 (P53617) SOLUTION NMR NMR measurement conditions:pH 8;293.15 K;Ionic strength (raw mmCIF value) 0.1;Pressure ambient NMR sample composition:1.5 mM Trf4p, 1 mM [U-99% 13C; U-99% 15N] Nrd1p, 100 mM sodium chloride, 50 mM sodium phosphate, 90% H2O/10% D2O | 90% H2O/10% D2O Resolution not provided

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PAP2_YEAST
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–12; UniProt 573–584

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 2mow

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2mow
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2mow
Deposition date deposition_date2014-05-06
Structure title titleStructure of Nrd1p CID - Trf4p NIM complex
Keywords keywordstranscription termination, RNA degradation, RNAP II CTD, protein-protein interaction, TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodSOLUTION NMR

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier17.32
Radius of gyration Rg (electron density) rg_electron16.32
Forward intensity I(0) i02296750000.00
Molecular weight molecular_weight393220.0 kDa
Excluded volume excluded_volume486130 ų
Envelope volume envelope_volume51908 ų
Hydration-shell volume shell_volume21518 ų
Envelope diameter envelope_diameter78.9
Shell Rg shell_rg27.36
Envelope Rg envelope_rg21.09
Shape Rg shape_rg16.32
Total Rg total_rg16.51
Total atoms total_atoms54440
Residues n_residues3460
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax65.8
Rg (real space) rg_real17.30
Rg uncertainty (real space) rg_real_error0.66
I(0) (real space) i0_real2.2970e+09
I(0) uncertainty (real space) i0_real_error3.3710e+07
Rg (reciprocal space) rg_reciprocal17.30
I(0) (reciprocal space) i0_reciprocal2297000000.0000
Solution quality estimate total_estimate0.6939
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks4
Primary peak position r_peak_primary22.5
Skewness Skewness skewness0.387
Kurtosis Kurtosis kurtosis0.121
Angular range angular_range— – 0.4600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha979900.0000
Real-space data points n_real_points77
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.407; Stabil: 0.971; Sysdev: 1.000; Positv: 1.000; Valcen: 0.883; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id2mowA00
Class class1 — Mainly Alpha
Architecture architecture25 — Alpha Horseshoe
Topology topology40 — Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat
Homologous superfamily homologous superfamily90

8. Citations (1)

9. Files and Curves (10)