2mgu

Structure of the complex between calmodulin and the binding domain of HIV-1 matrix protein

Method: SOLUTION NMR Dmax: 76.0 Å Quality: GOOD

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

Calmodulin

Rattus norvegicus

UniProt P62161

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 2–149 Not recorded MA8-43 × 1 (Q7ZJG2) CA CALCIUM ION × 4 SOLUTION NMR NMR measurement conditions:pH 6.3;308 K;Ionic strength (raw mmCIF value) 0.015;Pressure ambient NMR sample composition:0.1-1.2 mM [U-95% 13C; U-95% 15N] calmodulin, 0.1-1.2 mM MA8-43, 5 mM CALCIUM ION, 100% D2O | 100% 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.

22 other PDB entries and 47 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CALM_RAT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–148; UniProt 2–149

MA8-43

Human immunodeficiency virus 1

UniProt Q7ZJG2

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 M; UniProt 8–43 Not recorded Calmodulin × 1 (P62161) CA CALCIUM ION × 4 SOLUTION NMR NMR measurement conditions:pH 6.3;308 K;Ionic strength (raw mmCIF value) 0.015;Pressure ambient NMR sample composition:0.1-1.2 mM [U-95% 13C; U-95% 15N] calmodulin, 0.1-1.2 mM MA8-43, 5 mM CALCIUM ION, 100% D2O | 100% 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.

No other PDB entry for the same UniProt protein was found.

View Construct and Data Evidence
UniProt name Q7ZJG2_9HIV1
Isoform
PDB entities 2
Chains and sequence ranges Author chain M; PDBConstruct 1–36; UniProt 8–43

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 2mgu

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2mgu
Deposition date deposition_date2013-11-07
Structure title titleStructure of the complex between calmodulin and the binding domain of HIV-1 matrix protein
Keywords keywordscalmodulin, HIV-1 matrix, PROTEIN BINDING; PROTEIN BINDING
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier22.44
Radius of gyration Rg (electron density) rg_electron21.97
Forward intensity I(0) i02710770000.00
Molecular weight molecular_weight422390.0 kDa
Excluded volume excluded_volume520740 ų
Envelope volume envelope_volume122780 ų
Hydration-shell volume shell_volume37492 ų
Envelope diameter envelope_diameter83.0
Shell Rg shell_rg35.00
Envelope Rg envelope_rg26.43
Shape Rg shape_rg21.97
Total Rg total_rg22.28
Total atoms total_atoms57780
Residues n_residues3680
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 dmax76.0
Rg (real space) rg_real22.41
Rg uncertainty (real space) rg_real_error0.59
I(0) (real space) i0_real2.7110e+09
I(0) uncertainty (real space) i0_real_error3.7660e+07
Rg (reciprocal space) rg_reciprocal22.42
I(0) (reciprocal space) i0_reciprocal2711000000.0000
Solution quality estimate total_estimate0.8818
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary21.9
Skewness Skewness skewness0.224
Kurtosis Kurtosis kurtosis-0.661
Angular range angular_range— – 0.3550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4094000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.835; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.955; Smooth: 0.999

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 1 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2mgua_
Class classa — All alpha proteins
Fold Fold folda.39 — EF Hand-like
Superfamily Superfamily superfamilya.39.1 — EF-hand
Family Family familya.39.1.5 — Calmodulin-like

8. Citations (1)

9. Files and Curves (10)