3ikq

Crystal structure of alpha 1-2 mannobiose bound trimeric human lung surfactant protein D

Method: X-RAY DIFFRACTION Dmax: 75.8 Å Quality: REASONABLE

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

Pulmonary surfactant-associated protein D

Homo sapiens

UniProt P35247

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 homooligomer Homooligomer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 199–375 Chain B; UniProt 199–375 Chain C; UniProt 199–375 Fragment:UNP residues 199-375 Mutation:P180S CA CALCIUM ION × 10 MAN alpha-D-mannopyranose × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8;293 K;PEG 4000, tris, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 2.25 Å R-free 0.239

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.

30 other PDB entries and 36 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SFTPD_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–177; UniProt 199–375 Author chain B; PDBConstruct 1–177; UniProt 199–375 Author chain C; PDBConstruct 1–177; UniProt 199–375

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 3ikq

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3ikq
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3ikq
Deposition date deposition_date2009-08-06
Structure title titleCrystal structure of alpha 1-2 mannobiose bound trimeric human lung surfactant protein D
Keywords keywords;Trimeric recombinant fragment, neck+CRD, Collagen, Disulfide bond, Extracellular matrix, Gaseous exchange, Glycoprotein, Hydroxylation, Lectin, Secreted, Surface film, SUGAR BINDING PROTEIN ;; SUGAR BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.13
Radius of gyration Rg (electron density) rg_electron24.79
Forward intensity I(0) i040944800.00
Molecular weight molecular_weight48323.0 kDa
Excluded volume excluded_volume59971 ų
Envelope volume envelope_volume72059 ų
Hydration-shell volume shell_volume25141 ų
Envelope diameter envelope_diameter75.5
Shell Rg shell_rg31.07
Envelope Rg envelope_rg24.78
Shape Rg shape_rg24.75
Total Rg total_rg25.66
Total atoms total_atoms3382
Residues n_residues437
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 dmax75.8
Rg (real space) rg_real26.00
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real4.0940e+07
I(0) uncertainty (real space) i0_real_error5.1330e+05
Rg (reciprocal space) rg_reciprocal26.04
I(0) (reciprocal space) i0_reciprocal40950000.0000
Solution quality estimate total_estimate0.7069
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary38.5
Skewness Skewness skewness0.019
Kurtosis Kurtosis kurtosis-0.802
Angular range angular_range— – 0.3050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha13830000.0000
Real-space data points n_real_points62
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.977; Stabil: 1.000; Sysdev: 0.105; Positv: 1.000; Valcen: 0.997; Smooth: 0.943

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 9 domains

SCOP 2.08 (6 domains)

Domain ID domain_idd3ikqa1
Class classh — Coiled coil proteins
Fold Fold foldh.1 — Parallel coiled-coil
Superfamily Superfamily superfamilyh.1.1 — Triple coiled coil domain of C-type lectins
Family Family familyh.1.1.1 — Triple coiled coil domain of C-type lectins
Domain ID domain_idd3ikqa2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.169 — C-type lectin-like
Superfamily Superfamily superfamilyd.169.1 — C-type lectin-like
Family Family familyd.169.1.1 — C-type lectin domain
Domain ID domain_idd3ikqb1
Class classh — Coiled coil proteins
Fold Fold foldh.1 — Parallel coiled-coil
Superfamily Superfamily superfamilyh.1.1 — Triple coiled coil domain of C-type lectins
Family Family familyh.1.1.1 — Triple coiled coil domain of C-type lectins
Domain ID domain_idd3ikqb2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.169 — C-type lectin-like
Superfamily Superfamily superfamilyd.169.1 — C-type lectin-like
Family Family familyd.169.1.1 — C-type lectin domain
Domain ID domain_idd3ikqc1
Class classh — Coiled coil proteins
Fold Fold foldh.1 — Parallel coiled-coil
Superfamily Superfamily superfamilyh.1.1 — Triple coiled coil domain of C-type lectins
Family Family familyh.1.1.1 — Triple coiled coil domain of C-type lectins
Domain ID domain_idd3ikqc2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.169 — C-type lectin-like
Superfamily Superfamily superfamilyd.169.1 — C-type lectin-like
Family Family familyd.169.1.1 — C-type lectin domain

CATH v4.4 (3 domains)

Domain ID domain_id3ikqA00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology100 — Mannose-Binding Protein A; Chain A
Homologous superfamily homologous superfamily10 — Mannose-Binding Protein A, subunit A
Domain ID domain_id3ikqB00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology100 — Mannose-Binding Protein A; Chain A
Homologous superfamily homologous superfamily10 — Mannose-Binding Protein A, subunit A
Domain ID domain_id3ikqC00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology100 — Mannose-Binding Protein A; Chain A
Homologous superfamily homologous superfamily10 — Mannose-Binding Protein A, subunit A

8. Citations (2)

9. Files and Curves (10)