2p80

Solution structure of the complex between nitrite reductase and pseudoazurin from A. faecalis

Method: SOLUTION NMR Dmax: 98.3 Å Quality: GOOD

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

Copper-containing nitrite reductase

Alcaligenes faecalis

UniProt P38501

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 40–376 Chain B; UniProt 40–376 Chain C; UniProt 40–376 Not recorded Pseudoazurin × 1 (P04377) CU COPPER (II) ION × 7 GD GADOLINIUM ATOM × 9 SOLUTION NMR NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound GdCLaNP at position 221/223 (0.38 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound YCLaNP at position 221/223 (0.38 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound GdCLaNP at position 234/236 (0.32 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound YCLaNP at position 234/236 (0.32 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound GdCLaNP at position 333/336 (0.53 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound YCLaNP at position 333/336 (0.53 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) 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.

46 other PDB entries and 46 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NIR_ALCFA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–337; UniProt 40–376 Author chain B; PDBConstruct 1–337; UniProt 40–376 Author chain C; PDBConstruct 1–337; UniProt 40–376

Pseudoazurin

Alcaligenes faecalis

UniProt P04377

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain D; UniProt 24–146 Not recorded Copper-containing nitrite reductase × 3 (P38501) CU COPPER (II) ION × 7 GD GADOLINIUM ATOM × 9 SOLUTION NMR NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR measurement conditions:pH 6.5;298 K;Ionic strength (raw mmCIF value) 50 mM phosphate;Pressure 1 NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound GdCLaNP at position 221/223 (0.38 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound YCLaNP at position 221/223 (0.38 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound GdCLaNP at position 234/236 (0.32 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound YCLaNP at position 234/236 (0.32 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound GdCLaNP at position 333/336 (0.53 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) D2O NMR sample composition:250 mM 15N, 2H pseudoazurin in complex with nitrite reductase -bound YCLaNP at position 333/336 (0.53 eq), in 50 mM phosphate buffer, H2O, 6% (v/v) D2O | H2O, 6% (v/v) 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.

16 other PDB entries and 17 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name AZUP_ALCFA
Isoform
PDB entities 2
Chains and sequence ranges Author chain D; PDBConstruct 1–123; UniProt 24–146

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 2p80

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2p80
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2p80
Deposition date deposition_date2007-03-21
Structure title titleSolution structure of the complex between nitrite reductase and pseudoazurin from A. faecalis
Keywords keywordstransient complex, protein-protein interaction, redox partners, electron transfer, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier30.24
Radius of gyration Rg (electron density) rg_electron30.01
Forward intensity I(0) i084701900000.00
Molecular weight molecular_weight2478000.0 kDa
Excluded volume excluded_volume3079700 ų
Envelope volume envelope_volume188020 ų
Hydration-shell volume shell_volume49223 ų
Envelope diameter envelope_diameter108.9
Shell Rg shell_rg39.06
Envelope Rg envelope_rg31.20
Shape Rg shape_rg29.92
Total Rg total_rg30.35
Total atoms total_atoms341440
Residues n_residues22600
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 dmax98.3
Rg (real space) rg_real30.13
Rg uncertainty (real space) rg_real_error0.58
I(0) (real space) i0_real8.4700e+10
I(0) uncertainty (real space) i0_real_error1.2640e+09
Rg (reciprocal space) rg_reciprocal30.18
I(0) (reciprocal space) i0_reciprocal84710000000.0000
Solution quality estimate total_estimate0.8844
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary37.8
Skewness Skewness skewness0.287
Kurtosis Kurtosis kurtosis-0.236
Angular range angular_range— – 0.2600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha66890000.0000
Real-space data points n_real_points53
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.853; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.937

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 14 domains

SCOP 2.08 (7 domains)

Domain ID domain_idd2p80a1
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.0 — automated matches
Domain ID domain_idd2p80a2
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.0 — automated matches
Domain ID domain_idd2p80b1
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.0 — automated matches
Domain ID domain_idd2p80b2
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.0 — automated matches
Domain ID domain_idd2p80c1
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.0 — automated matches
Domain ID domain_idd2p80c2
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.0 — automated matches
Domain ID domain_idd2p80d_
Class classb — All beta proteins
Fold Fold foldb.6 — Cupredoxin-like
Superfamily Superfamily superfamilyb.6.1 — Cupredoxins
Family Family familyb.6.1.1 — Plastocyanin/azurin-like

CATH v4.4 (7 domains)

Domain ID domain_id2p80A01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins
Domain ID domain_id2p80A02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins
Domain ID domain_id2p80B01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins
Domain ID domain_id2p80B02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins
Domain ID domain_id2p80C01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins
Domain ID domain_id2p80C02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily420 — Cupredoxins - blue copper proteins
Domain ID domain_id2p80D00
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)