3esa

cut-1b; NCN-Pt-Pincer-Cutinase Hybrid

Method: X-RAY DIFFRACTION Dmax: 92.0 Å Quality: GOOD

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

Cutinase 1

Fusarium solani f. pisi

UniProt P00590

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 17–230 Mutation:N172K NXC (2,6-bis[(dimethylamino-kappaN)methyl]-4-{3-[(S)-ethoxy(4-nitrophenoxy)phosphoryl]propyl}phenyl-kappaC~1~)(chloro)platinum(2+) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 5.5;291 K;22%(w/v) PEG-6000, 0.1M sodium acetate, 0.2M sodium chloride, pH 5.5, VAPOR DIFFUSION, temperature 291K Resolution 2.00 Å R-free 0.253
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 17–230 Mutation:N172K NXC (2,6-bis[(dimethylamino-kappaN)methyl]-4-{3-[(S)-ethoxy(4-nitrophenoxy)phosphoryl]propyl}phenyl-kappaC~1~)(chloro)platinum(2+) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 5.5;291 K;22%(w/v) PEG-6000, 0.1M sodium acetate, 0.2M sodium chloride, pH 5.5, VAPOR DIFFUSION, temperature 291K Resolution 2.00 Å R-free 0.253

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.

43 other PDB entries and 48 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CUTI1_FUSSO
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–214; UniProt 17–230 Author chain B; PDBConstruct 1–214; UniProt 17–230

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 3esa

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id3esa
Deposition date deposition_date2008-10-05
Structure title titlecut-1b; NCN-Pt-Pincer-Cutinase Hybrid
Keywords keywordsprotein-metallopincer complex, Glycoprotein, Hydrolase, Secreted, Serine esterase; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.55
Radius of gyration Rg (electron density) rg_electron26.17
Forward intensity I(0) i031919600.00
Molecular weight molecular_weight42054.0 kDa
Excluded volume excluded_volume51910 ų
Envelope volume envelope_volume60600 ų
Hydration-shell volume shell_volume20925 ų
Envelope diameter envelope_diameter92.2
Shell Rg shell_rg31.04
Envelope Rg envelope_rg26.48
Shape Rg shape_rg26.26
Total Rg total_rg26.45
Total atoms total_atoms2927
Residues n_residues394
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 dmax92.0
Rg (real space) rg_real26.90
Rg uncertainty (real space) rg_real_error0.72
I(0) (real space) i0_real3.1920e+07
I(0) uncertainty (real space) i0_real_error4.9620e+05
Rg (reciprocal space) rg_reciprocal26.79
I(0) (reciprocal space) i0_reciprocal31920000.0000
Solution quality estimate total_estimate0.7553
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.0
Skewness Skewness skewness0.576
Kurtosis Kurtosis kurtosis-0.450
Angular range angular_range— – 0.3000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha20390000.0000
Real-space data points n_real_points61
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.465; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.471; Smooth: 0.949

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3esaa_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.69 — alpha/beta-Hydrolases
Superfamily Superfamily superfamilyc.69.1 — alpha/beta-Hydrolases
Family Family familyc.69.1.30 — Cutinase-like
Domain ID domain_idd3esab_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.69 — alpha/beta-Hydrolases
Superfamily Superfamily superfamilyc.69.1 — alpha/beta-Hydrolases
Family Family familyc.69.1.30 — Cutinase-like

CATH v4.4 (2 domains)

Domain ID domain_id3esaA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1820 — Alpha/Beta hydrolase fold, catalytic domain
Domain ID domain_id3esaB00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1820 — Alpha/Beta hydrolase fold, catalytic domain

8. Citations (1)

9. Files and Curves (10)