3oud

MDR769 HIV-1 protease complexed with CA/p2 hepta-peptide

Method: X-RAY DIFFRACTION Dmax: 69.6 Å Quality: REASONABLE

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

MDR HIV-1 protease

Human immunodeficiency virus 1

UniProt Q000H7

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 1–99 Chain B; UniProt 1–99 Not recorded CA/p2 substrate peptide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.8;298 K;0.8M NaCl 0.1 M MES , pH 5.8, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.80 Å R-free 0.244

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.

20 other PDB entries and 20 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q000H7_9HIV1
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–99; UniProt 1–99 Author chain B; PDBConstruct 1–99; UniProt 1–99

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 3oud

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id3oud
Deposition date deposition_date2010-09-14
Structure title titleMDR769 HIV-1 protease complexed with CA/p2 hepta-peptide
Keywords keywords;MDR HIV-1 protease, inhibitor, drug resistance, substrate envelope, HIV-1 protease, protease, CA/p2 substrate peptide, none, HYDROLASE, HYDROLASE-PEPTIDE complex ;; HYDROLASE/PEPTIDE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.50
Radius of gyration Rg (electron density) rg_electron17.66
Forward intensity I(0) i08477830.00
Molecular weight molecular_weight22589.0 kDa
Excluded volume excluded_volume28863 ų
Envelope volume envelope_volume33277 ų
Hydration-shell volume shell_volume16161 ų
Envelope diameter envelope_diameter67.0
Shell Rg shell_rg23.40
Envelope Rg envelope_rg18.01
Shape Rg shape_rg17.72
Total Rg total_rg18.44
Total atoms total_atoms1570
Residues n_residues203
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 dmax69.6
Rg (real space) rg_real18.50
Rg uncertainty (real space) rg_real_error0.52
I(0) (real space) i0_real8.4780e+06
I(0) uncertainty (real space) i0_real_error1.0500e+05
Rg (reciprocal space) rg_reciprocal18.50
I(0) (reciprocal space) i0_reciprocal8478000.0000
Solution quality estimate total_estimate0.7316
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.0
Skewness Skewness skewness0.391
Kurtosis Kurtosis kurtosis-0.168
Angular range angular_range— – 0.4300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4324000.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.541; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.883; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3ouda_
Class classb — All beta proteins
Fold Fold foldb.50 — Acid proteases
Superfamily Superfamily superfamilyb.50.1 — Acid proteases
Family Family familyb.50.1.1 — Retroviral protease (retropepsin)
Domain ID domain_idd3oudb_
Class classb — All beta proteins
Fold Fold foldb.50 — Acid proteases
Superfamily Superfamily superfamilyb.50.1 — Acid proteases
Family Family familyb.50.1.1 — Retroviral protease (retropepsin)

CATH v4.4 (2 domains)

Domain ID domain_id3oudA00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology70 — Cathepsin D, subunit A; domain 1
Homologous superfamily homologous superfamily10 — Acid Proteases
Domain ID domain_id3oudB00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology70 — Cathepsin D, subunit A; domain 1
Homologous superfamily homologous superfamily10 — Acid Proteases

8. Citations (1)

9. Files and Curves (10)