4ae3

Crystal structure of ammosamide 272:myosin-2 motor domain complex

Method: X-RAY DIFFRACTION Dmax: 99.3 Å Quality: GOOD

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

MYOSIN-2 HEAVY CHAIN

DICTYOSTELIUM DISCOIDEUM

UniProt P08799

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 2–761 Fragment:MOTOR DOMAIN, RESIDUES 2-761 AOV ADP ORTHOVANADATE × 1 MG MAGNESIUM ION × 1 27X AMMOSAMIDE 272 × 2 EDO 1,2-ETHANEDIOL × 4 X-RAY DIFFRACTION X-ray crystallization conditions:50 MM HEPES PH 7.6, 140 MM NACL, 11% W/V PEG5K-MME, 2% (V/V) MPD Resolution 2.50 Å R-free 0.254

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.

48 other PDB entries and 52 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MYS2_DICDI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–760; UniProt 2–761

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 4ae3

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4ae3
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4ae3
Deposition date deposition_date2012-01-05
Structure title titleCrystal structure of ammosamide 272:myosin-2 motor domain complex
Keywords keywordsHYDROLASE, ATPASE, CONTRACTILE PROTEIN, ACTIN BINDING, MOTOR PROTEIN; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier29.75
Radius of gyration Rg (electron density) rg_electron29.02
Forward intensity I(0) i0116867000.00
Molecular weight molecular_weight85814.0 kDa
Excluded volume excluded_volume107550 ų
Envelope volume envelope_volume134680 ų
Hydration-shell volume shell_volume38441 ų
Envelope diameter envelope_diameter106.7
Shell Rg shell_rg36.36
Envelope Rg envelope_rg29.56
Shape Rg shape_rg29.03
Total Rg total_rg29.69
Total atoms total_atoms6052
Residues n_residues743
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 dmax99.3
Rg (real space) rg_real29.75
Rg uncertainty (real space) rg_real_error0.73
I(0) (real space) i0_real1.1690e+08
I(0) uncertainty (real space) i0_real_error1.8830e+06
Rg (reciprocal space) rg_reciprocal29.75
I(0) (reciprocal space) i0_reciprocal116900000.0000
Solution quality estimate total_estimate0.8790
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary97.5
Skewness Skewness skewness0.403
Kurtosis Kurtosis kurtosis-0.199
Angular range angular_range— – 0.2650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha20030000.0000
Real-space data points n_real_points54
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.823; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.997; Smooth: 0.957

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id4ae3A01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology58 — Methane Monooxygenase Hydroxylase; Chain G, domain 1
Homologous superfamily homologous superfamily530
Domain ID domain_id4ae3A02
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology58 — Methane Monooxygenase Hydroxylase; Chain G, domain 1
Homologous superfamily homologous superfamily60

8. Citations (1)

9. Files and Curves (10)