1ygw

NMR STRUCTURE OF RIBONUCLEASE T1, 34 STRUCTURES

Method: SOLUTION NMR Dmax: 32.4 Å Quality: EXCELLENT

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

RIBONUCLEASE T1

Aspergillus oryzae

UniProt P00651

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 22–125 Mutation:ISOENZYME WITH LYSINE AT POSITION 25 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 5.5;313 K 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.

67 other PDB entries and 100 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RNT1_ASPOR
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–104; UniProt 22–125

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 1ygw

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1ygw
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1ygw
Deposition date deposition_date1996-09-28
Structure title titleNMR STRUCTURE OF RIBONUCLEASE T1, 34 STRUCTURES
Keywords keywordsHYDROLASE, RIBONUCLEASE, ENDONUCLEASE, RIBONUCLEASE T1 PRECURSOR, ENDORIBONUCLEASE; HYDROLASE
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier12.36
Radius of gyration Rg (electron density) rg_electron11.92
Forward intensity I(0) i02317630000.00
Molecular weight molecular_weight376130.0 kDa
Excluded volume excluded_volume453910 ų
Envelope volume envelope_volume18151 ų
Hydration-shell volume shell_volume11735 ų
Envelope diameter envelope_diameter41.0
Shell Rg shell_rg18.92
Envelope Rg envelope_rg13.24
Shape Rg shape_rg11.87
Total Rg total_rg12.15
Total atoms total_atoms49606
Residues n_residues3536
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 dmax32.4
Rg (real space) rg_real12.23
Rg uncertainty (real space) rg_real_error0.16
I(0) (real space) i0_real2.3180e+09
I(0) uncertainty (real space) i0_real_error2.1850e+07
Rg (reciprocal space) rg_reciprocal12.24
I(0) (reciprocal space) i0_reciprocal2318000000.0000
Solution quality estimate total_estimate0.9056
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary15.2
Skewness Skewness skewness-0.069
Kurtosis Kurtosis kurtosis-0.576
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha184900.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.994; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.993; Smooth: 0.799

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1ygwa_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.1 — Microbial ribonucleases
Superfamily Superfamily superfamilyd.1.1 — Microbial ribonucleases
Family Family familyd.1.1.4 — Fungal ribonucleases

CATH v4.4 (1 domains)

Domain ID domain_id1ygwA00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology450 — Nuclear Transport Factor 2; Chain: A,
Homologous superfamily homologous superfamily30 — Microbial ribonucleases

8. Citations (3)

9. Files and Curves (10)