1k88

Crystal structure of procaspase-7

Method: X-RAY DIFFRACTION Dmax: 72.0 Å Quality: EXCELLENT

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

procaspase-7

Homo sapiens

UniProt P55210

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 51–303 Chain B; UniProt 51–303 Fragment:procaspase-7 Mutation:C186A No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.8;296 K;lithium sulfate, sodium chloride, pH 5.8, VAPOR DIFFUSION, HANGING DROP, temperature 296K Resolution 2.70 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.

46 other PDB entries and 54 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CASP7_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–253; UniProt 51–303 Author chain B; PDBConstruct 1–253; UniProt 51–303

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 1k88

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1k88
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1k88
Deposition date deposition_date2001-10-23
Structure title titleCrystal structure of procaspase-7
Keywords keywordsprocaspase activation, apoptosis, protease, substrate binding; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.44
Radius of gyration Rg (electron density) rg_electron22.06
Forward intensity I(0) i045998000.00
Molecular weight molecular_weight52544.0 kDa
Excluded volume excluded_volume65721 ų
Envelope volume envelope_volume76871 ų
Hydration-shell volume shell_volume28133 ų
Envelope diameter envelope_diameter74.4
Shell Rg shell_rg29.80
Envelope Rg envelope_rg22.36
Shape Rg shape_rg22.07
Total Rg total_rg22.93
Total atoms total_atoms3692
Residues n_residues461
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 dmax72.0
Rg (real space) rg_real23.28
Rg uncertainty (real space) rg_real_error0.32
I(0) (real space) i0_real4.6000e+07
I(0) uncertainty (real space) i0_real_error5.7190e+05
Rg (reciprocal space) rg_reciprocal23.32
I(0) (reciprocal space) i0_reciprocal46000000.0000
Solution quality estimate total_estimate0.9018
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.8
Skewness Skewness skewness0.128
Kurtosis Kurtosis kurtosis-0.511
Angular range angular_range— – 0.3400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7189000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.923; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.985; Smooth: 0.965

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1k88a_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.17 — Caspase-like
Superfamily Superfamily superfamilyc.17.1 — Caspase-like
Family Family familyc.17.1.1 — Caspase catalytic domain
Domain ID domain_idd1k88b_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.17 — Caspase-like
Superfamily Superfamily superfamilyc.17.1 — Caspase-like
Family Family familyc.17.1.1 — Caspase catalytic domain

CATH v4.4 (2 domains)

Domain ID domain_id1k88A00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1460
Domain ID domain_id1k88B00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1460

8. Citations (1)

9. Files and Curves (10)