1m4a

Crystal Structure of Human Interleukin-2 Y31C Covalently Modified at C31 with (1H-Indol-3-yl)-(2-mercapto-ethoxyimino)-acetic acid

Method: X-RAY DIFFRACTION Dmax: 51.7 Å Quality: GOOD

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

interleukin-2

Homo sapiens

UniProt P60568

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 21–153 Mutation:Y31C MPE (1H-INDOL-3-YL)-(2-MERCAPTO-ETHOXYIMINO)-ACETIC ACID × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;298 K;pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 2.18 Å R-free 0.324

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.

33 other PDB entries and 77 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name IL2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–133; UniProt 21–153

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 1m4a

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1m4a
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1m4a
Deposition date deposition_date2002-07-02
Structure title titleCrystal Structure of Human Interleukin-2 Y31C Covalently Modified at C31 with (1H-Indol-3-yl)-(2-mercapto-ethoxyimino)-acetic acid
Keywords keywordscytokine, four-helix bundle, small molecule complex; CYTOKINE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.56
Radius of gyration Rg (electron density) rg_electron14.24
Forward intensity I(0) i03426540.00
Molecular weight molecular_weight13721.0 kDa
Excluded volume excluded_volume17553 ų
Envelope volume envelope_volume19680 ų
Hydration-shell volume shell_volume11942 ų
Envelope diameter envelope_diameter53.8
Shell Rg shell_rg19.80
Envelope Rg envelope_rg14.72
Shape Rg shape_rg14.19
Total Rg total_rg15.61
Total atoms total_atoms959
Residues n_residues114
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 dmax51.7
Rg (real space) rg_real15.49
Rg uncertainty (real space) rg_real_error0.35
I(0) (real space) i0_real3.4270e+06
I(0) uncertainty (real space) i0_real_error4.3540e+04
Rg (reciprocal space) rg_reciprocal15.50
I(0) (reciprocal space) i0_reciprocal3427000.0000
Solution quality estimate total_estimate0.7955
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary19.6
Skewness Skewness skewness0.205
Kurtosis Kurtosis kurtosis-0.247
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha524800.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.781; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1m4aa_
Class classa — All alpha proteins
Fold Fold folda.26 — 4-helical cytokines
Superfamily Superfamily superfamilya.26.1 — 4-helical cytokines
Family Family familya.26.1.2 — Short-chain cytokines

CATH v4.4 (1 domains)

Domain ID domain_id1m4aA00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1250 — Growth Hormone; Chain: A;
Homologous superfamily homologous superfamily10

8. Citations (1)

9. Files and Curves (10)