1u4s

Plasmodium falciparum lactate dehydrogenase complexed with 2,6-naphthalenedisulphonic acid

Method: X-RAY DIFFRACTION Dmax: 68.4 Å Quality: GOOD

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

L-lactate dehydrogenase

Plasmodium falciparum

UniProt Q27743

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 2–316 Not recorded BIH NAPHTHALENE-2,6-DISULFONIC ACID × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;291 K;MPD, Hepes, Imidazole, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 291K Resolution 2.00 Å R-free 0.188

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.

15 other PDB entries and 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LDH1_PLAFD
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–315; UniProt 2–316

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 1u4s

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1u4s
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1u4s
Deposition date deposition_date2004-07-26
Structure title titlePlasmodium falciparum lactate dehydrogenase complexed with 2,6-naphthalenedisulphonic acid
Keywords keywordsProtein-ligand complex, OXIDOREDUCTASE; OXIDOREDUCTASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.58
Radius of gyration Rg (electron density) rg_electron19.43
Forward intensity I(0) i018467600.00
Molecular weight molecular_weight33386.0 kDa
Excluded volume excluded_volume42264 ų
Envelope volume envelope_volume48566 ų
Hydration-shell volume shell_volume20884 ų
Envelope diameter envelope_diameter69.5
Shell Rg shell_rg25.96
Envelope Rg envelope_rg19.62
Shape Rg shape_rg19.45
Total Rg total_rg20.30
Total atoms total_atoms2340
Residues n_residues301
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 dmax68.4
Rg (real space) rg_real20.49
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real1.8470e+07
I(0) uncertainty (real space) i0_real_error2.2900e+05
Rg (reciprocal space) rg_reciprocal20.51
I(0) (reciprocal space) i0_reciprocal18470000.0000
Solution quality estimate total_estimate0.8833
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.8
Skewness Skewness skewness0.218
Kurtosis Kurtosis kurtosis-0.354
Angular range angular_range— – 0.3850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3432000.0000
Real-space data points n_real_points70
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.828; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.995

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 5 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1u4sa1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.2 — NAD(P)-binding Rossmann-fold domains
Superfamily Superfamily superfamilyc.2.1 — NAD(P)-binding Rossmann-fold domains
Family Family familyc.2.1.5 — LDH N-terminal domain-like
Domain ID domain_idd1u4sa2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.162 — LDH C-terminal domain-like
Superfamily Superfamily superfamilyd.162.1 — LDH C-terminal domain-like
Family Family familyd.162.1.1 — Lactate & malate dehydrogenases, C-terminal domain
Domain ID domain_idd1u4sa3
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (2 domains)

Domain ID domain_id1u4sA01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily720 — NAD(P)-binding Rossmann-like Domain
Domain ID domain_id1u4sA02
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology110 — L-2-Hydroxyisocaproate Dehydrogenase; Chain A, domain 2
Homologous superfamily homologous superfamily10 — Lactate dehydrogenase/glycoside hydrolase, family 4, C-terminal

8. Citations (1)

9. Files and Curves (10)