2ipp

Crystal Structure of the tetragonal form of human liver cathepsin B

Method: X-RAY DIFFRACTION Dmax: 58.3 Å Quality: GOOD

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

Cathepsin B

OrganismNot specified

UniProt P07858

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 80–126 Chain B; UniProt 129–333 Fragment:light chain, residues 80-126 Fragment:heavy chain, residues 129-333 PYS 2-PYRIDINETHIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4;293 K;pH 4.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K Resolution 2.15 Å

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 29 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CATB_HUMAN
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–47; UniProt 80–126 Author chain B; PDBConstruct 1–205; UniProt 129–333

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 2ipp

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2ipp
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2ipp
Deposition date deposition_date2006-10-12
Structure title titleCrystal Structure of the tetragonal form of human liver cathepsin B
Keywords keywordsCATHEPSIN, CYSTEINE PROTEINASE, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.23
Radius of gyration Rg (electron density) rg_electron17.22
Forward intensity I(0) i015077800.00
Molecular weight molecular_weight27725.0 kDa
Excluded volume excluded_volume33979 ų
Envelope volume envelope_volume38164 ų
Hydration-shell volume shell_volume18209 ų
Envelope diameter envelope_diameter59.6
Shell Rg shell_rg23.73
Envelope Rg envelope_rg17.57
Shape Rg shape_rg17.19
Total Rg total_rg18.26
Total atoms total_atoms1945
Residues n_residues252
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 dmax58.3
Rg (real space) rg_real18.12
Rg uncertainty (real space) rg_real_error0.29
I(0) (real space) i0_real1.5080e+07
I(0) uncertainty (real space) i0_real_error1.8630e+05
Rg (reciprocal space) rg_reciprocal18.14
I(0) (reciprocal space) i0_reciprocal15080000.0000
Solution quality estimate total_estimate0.8886
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary22.8
Skewness Skewness skewness0.164
Kurtosis Kurtosis kurtosis-0.373
Angular range angular_range— – 0.4350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3184000.0000
Real-space data points n_real_points75
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.862; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.989; Smooth: 0.974

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id2ippA01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology5 — Single alpha-helices involved in coiled-coils or other helix-helix interfaces
Homologous superfamily homologous superfamily170
Domain ID domain_id2ippB00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology70 — Cathepsin B; Chain A
Homologous superfamily homologous superfamily10 — Cysteine proteinases

8. Citations (1)

9. Files and Curves (10)