1wbr

SOLUTION STRUCTURE OF THE HUMAN CD4 (403-419) RECEPTOR PEPTIDE, NMR, 32 STRUCTURES

Method: SOLUTION NMR Dmax: 31.3 Å Quality: REASONABLE

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

CD4 RECEPTOR

Homo sapiens

UniProt P01730

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 428–444 Fragment:403 - 419 Mutation:N-TERMINUS IS ACETYLATED, C-TERMINUS IS AMIDATED Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer SOLUTION NMR NMR measurement conditions:pH 7;298 K 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.

78 other PDB entries and 99 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CD4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–18; UniProt 428–444

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 1wbr

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1wbr
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id1wbr
Deposition date deposition_date1996-12-20
Structure title titleSOLUTION STRUCTURE OF THE HUMAN CD4 (403-419) RECEPTOR PEPTIDE, NMR, 32 STRUCTURES
Keywords keywordsIMMUNOGLOBULIN FOLD, CD4(403-419) RECEPTOR PEPTIDE, HIV, VPU; IMMUNOGLOBULIN FOLD
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier7.55
Radius of gyration Rg (electron density) rg_electron8.21
Forward intensity I(0) i067171700.00
Molecular weight molecular_weight66928.0 kDa
Excluded volume excluded_volume83939 ų
Envelope volume envelope_volume7671 ų
Hydration-shell volume shell_volume6799 ų
Envelope diameter envelope_diameter34.3
Shell Rg shell_rg15.24
Envelope Rg envelope_rg10.61
Shape Rg shape_rg8.15
Total Rg total_rg8.64
Total atoms total_atoms9824
Residues n_residues544
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 dmax31.3
Rg (real space) rg_real7.63
Rg uncertainty (real space) rg_real_error0.49
I(0) (real space) i0_real6.7170e+07
I(0) uncertainty (real space) i0_real_error6.5550e+05
Rg (reciprocal space) rg_reciprocal7.63
I(0) (reciprocal space) i0_reciprocal67170000.0000
Solution quality estimate total_estimate0.7299
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary7.1
Skewness Skewness skewness0.512
Kurtosis Kurtosis kurtosis-0.107
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2350.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.462; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.155; Smooth: 0.943

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 1 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1wbra_
Class classj — Peptides
Fold Fold foldj.48 — CD4 and CD8 receptor regions
Superfamily Superfamily superfamilyj.48.1 — CD4 and CD8 receptor regions
Family Family familyj.48.1.1 — CD4 and CD8 receptor regions

8. Citations (1)

9. Files and Curves (10)