2lln

Solution structure of Thermus thermophilus apo-CuA

Method: SOLUTION NMR Dmax: 49.2 Å Quality: GOOD

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

Cytochrome c oxidase subunit 2

Thermus thermophilus

UniProt P98052

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 11–135 Fragment:UNP residues 11-135 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6;298 K;Ionic strength (raw mmCIF value) 0.1;Pressure ambient NMR sample composition:0.8 -1 mM [U-99% 13C; U-99% 15N] protein, 100 mM potassium phosphate, 2 mM DTT, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:0.8 -1 mM [U-99% 15N] protein, 100 mM potassium phosphate, 2 mM DTT, 90% H2O/10% D2O | 90% H2O/10% D2O NMR sample composition:0.8 - 1 mM protein, 100 mM potassium phosphate, 2 mM DTT, 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.

6 other PDB entries and 16 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name COX2_THETH
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–126; UniProt 11–135

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 2lln

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2lln
Deposition date deposition_date2011-11-15
Structure title titleSolution structure of Thermus thermophilus apo-CuA
Keywords keywordsentatic state, electron transfer, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier14.67
Radius of gyration Rg (electron density) rg_electron14.34
Forward intensity I(0) i01019520000.00
Molecular weight molecular_weight278560.0 kDa
Excluded volume excluded_volume351070 ų
Envelope volume envelope_volume31491 ų
Hydration-shell volume shell_volume16170 ų
Envelope diameter envelope_diameter56.5
Shell Rg shell_rg22.43
Envelope Rg envelope_rg16.53
Shape Rg shape_rg14.30
Total Rg total_rg14.63
Total atoms total_atoms39020
Residues n_residues2520
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 dmax49.2
Rg (real space) rg_real14.56
Rg uncertainty (real space) rg_real_error0.33
I(0) (real space) i0_real1.0200e+09
I(0) uncertainty (real space) i0_real_error1.1040e+07
Rg (reciprocal space) rg_reciprocal14.57
I(0) (reciprocal space) i0_reciprocal1020000000.0000
Solution quality estimate total_estimate0.8799
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary19.3
Skewness Skewness skewness0.068
Kurtosis Kurtosis kurtosis-0.460
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha389800.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.813; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.996

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_idd2llna_
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.2 — Periplasmic domain of cytochrome c oxidase subunit II

CATH v4.4 (1 domains)

Domain ID domain_id2llnA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins

8. Citations (1)

9. Files and Curves (10)