2lnk

Solution structure of Ca-bound S100A4 in complex with non-muscle myosin IIA

Method: SOLUTION NMR Dmax: 70.9 Å Quality: GOOD

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

Myosin heavy chain, non-muscle IIa

OrganismNot specified

UniProt P35579

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 1897–1935 Fragment:UNP residues 1897-1935 Protein S100-A4 × 2 (P26447) SOLUTION NMR NMR measurement conditions:pH 6.1;313 K;Ionic strength (raw mmCIF value) 0.02;Pressure ambient NMR sample composition:0.5 mM protein_1, 1 mM [U-100% 13C; U-100% 15N] protein_2, 5 mM CALCIUM ION, 20 mM MES, 20 mM sodium chloride, 4 mM TCEP, 95% H2O/5% D2O | 95% H2O/5% 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.

7 other PDB entries and 8 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MYH9_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain C; PDBConstruct 1–39; UniProt 1897–1935

Protein S100-A4

Homo sapiens

UniProt P26447

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–101 Chain B; UniProt 1–101 Not recorded Myosin heavy chain, non-muscle IIa × 1 (P35579) SOLUTION NMR NMR measurement conditions:pH 6.1;313 K;Ionic strength (raw mmCIF value) 0.02;Pressure ambient NMR sample composition:0.5 mM protein_1, 1 mM [U-100% 13C; U-100% 15N] protein_2, 5 mM CALCIUM ION, 20 mM MES, 20 mM sodium chloride, 4 mM TCEP, 95% H2O/5% D2O | 95% H2O/5% 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 35 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name S10A4_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain A; PDBConstruct 13–113; UniProt 1–101 Author chain B; PDBConstruct 13–113; UniProt 1–101

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 2lnk

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2lnk
Deposition date deposition_date2011-12-30
Structure title titleSolution structure of Ca-bound S100A4 in complex with non-muscle myosin IIA
Keywords keywordsEF-hand, calcium binding, all alpha, METAL BINDING PROTEIN, CALCIUM BINDING PROTEIN; CALCIUM BINDING PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier17.89
Radius of gyration Rg (electron density) rg_electron17.38
Forward intensity I(0) i04437650000.00
Molecular weight molecular_weight559140.0 kDa
Excluded volume excluded_volume696480 ų
Envelope volume envelope_volume69344 ų
Hydration-shell volume shell_volume25941 ų
Envelope diameter envelope_diameter83.9
Shell Rg shell_rg29.61
Envelope Rg envelope_rg23.03
Shape Rg shape_rg17.38
Total Rg total_rg17.50
Total atoms total_atoms77900
Residues n_residues4820
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 dmax70.9
Rg (real space) rg_real17.82
Rg uncertainty (real space) rg_real_error0.51
I(0) (real space) i0_real4.4380e+09
I(0) uncertainty (real space) i0_real_error5.5930e+07
Rg (reciprocal space) rg_reciprocal17.82
I(0) (reciprocal space) i0_reciprocal4438000000.0000
Solution quality estimate total_estimate0.7741
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary69.0
Skewness Skewness skewness0.308
Kurtosis Kurtosis kurtosis-0.052
Angular range angular_range— – 0.4450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2348000.0000
Real-space data points n_real_points75
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.376; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.931; Smooth: 0.998

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id2lnkA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand
Domain ID domain_id2lnkB00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand

8. Citations (1)

9. Files and Curves (10)