5ka5

HIV-1 gp41 variant V549E resistance mutation

Method: X-RAY DIFFRACTION Dmax: 66.1 Å Quality: GOOD

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

Transmembrane glycoprotein gp41

Human immunodeficiency virus type 1

UniProt P04578

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 543–582 Chain A; UniProt 625–661 Fragment:UNP residues 543-582 and 625-661 linked via GGRGG Mutation:V549E No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.5;291 K;3M Sodium chloride, 0.1M Sodium Acetate Sample concentration: 6 mg/ml Resolution 1.80 Å R-free 0.223

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.

38 other PDB entries and 49 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ENV_HV1H2
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–41; UniProt 543–582 Author chain A; PDBConstruct 47–83; UniProt 625–661

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 5ka5

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5ka5
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5ka5
Deposition date deposition_date2016-06-01
Structure title titleHIV-1 gp41 variant V549E resistance mutation
Keywords keywordsHiv-1, membrane fusion, 5-helix, C-peptide, VIRAL PROTEIN; VIRAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier17.97
Radius of gyration Rg (electron density) rg_electron17.88
Forward intensity I(0) i01902230.00
Molecular weight molecular_weight9188.0 kDa
Excluded volume excluded_volume11322 ų
Envelope volume envelope_volume14461 ų
Hydration-shell volume shell_volume8229 ų
Envelope diameter envelope_diameter64.3
Shell Rg shell_rg20.48
Envelope Rg envelope_rg18.52
Shape Rg shape_rg17.83
Total Rg total_rg18.53
Total atoms total_atoms647
Residues n_residues79
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 dmax66.1
Rg (real space) rg_real18.38
Rg uncertainty (real space) rg_real_error0.76
I(0) (real space) i0_real1.9020e+06
I(0) uncertainty (real space) i0_real_error2.6970e+04
Rg (reciprocal space) rg_reciprocal18.33
I(0) (reciprocal space) i0_reciprocal1902000.0000
Solution quality estimate total_estimate0.7515
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary14.3
Skewness Skewness skewness0.640
Kurtosis Kurtosis kurtosis-0.257
Angular range angular_range— – 0.4450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha176300.0000
Real-space data points n_real_points75
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.525; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.194; Smooth: 0.995

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id5ka5A00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology287 — Helix Hairpins
Homologous superfamily homologous superfamily210

8. Citations (1)

9. Files and Curves (10)