1d1p

CRYSTAL STRUCTURE OF A YEAST LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE (LTP1)

Method: X-RAY DIFFRACTION Dmax: 75.7 Å Quality: REASONABLE

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

TYROSINE PHOSPHATASE

Saccharomyces cerevisiae

UniProt P40347

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 2–161 Not recorded EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;298 K;PEG 3400, HEPES, sodium chloride, pH 7.0, VAPOR DIFFUSION, SITTING DROP, temperature 298.0K Resolution 2.20 Å R-free 0.235
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 2–161 Not recorded EPE 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;298 K;PEG 3400, HEPES, sodium chloride, pH 7.0, VAPOR DIFFUSION, SITTING DROP, temperature 298.0K Resolution 2.20 Å R-free 0.235

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.

2 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PPAL_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–160; UniProt 2–161 Author chain B; PDBConstruct 1–160; UniProt 2–161

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 1d1p

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1d1p
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1d1p
Deposition date deposition_date1999-09-20
Structure title titleCRYSTAL STRUCTURE OF A YEAST LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE (LTP1)
Keywords keywordsBETA-ALPHA-BETA, TYROSINE PHOSPHATASE, LTP1, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.13
Radius of gyration Rg (electron density) rg_electron22.37
Forward intensity I(0) i023058800.00
Molecular weight molecular_weight36751.0 kDa
Excluded volume excluded_volume45967 ų
Envelope volume envelope_volume54418 ų
Hydration-shell volume shell_volume20905 ų
Envelope diameter envelope_diameter76.7
Shell Rg shell_rg28.46
Envelope Rg envelope_rg22.33
Shape Rg shape_rg22.37
Total Rg total_rg23.14
Total atoms total_atoms2589
Residues n_residues313
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 dmax75.7
Rg (real space) rg_real23.19
Rg uncertainty (real space) rg_real_error0.44
I(0) (real space) i0_real2.3060e+07
I(0) uncertainty (real space) i0_real_error2.8870e+05
Rg (reciprocal space) rg_reciprocal23.18
I(0) (reciprocal space) i0_reciprocal23060000.0000
Solution quality estimate total_estimate0.7292
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.3
Skewness Skewness skewness0.389
Kurtosis Kurtosis kurtosis-0.460
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4987000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.875; Stabil: 1.000; Sysdev: 0.307; Positv: 1.000; Valcen: 0.945; Smooth: 0.986

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_idd1d1pa_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.44 — Phosphotyrosine protein phosphatases I-like
Superfamily Superfamily superfamilyc.44.1 — Phosphotyrosine protein phosphatases I
Family Family familyc.44.1.1 — Low-molecular-weight phosphotyrosine protein phosphatases
Domain ID domain_idd1d1pb_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.44 — Phosphotyrosine protein phosphatases I-like
Superfamily Superfamily superfamilyc.44.1 — Phosphotyrosine protein phosphatases I
Family Family familyc.44.1.1 — Low-molecular-weight phosphotyrosine protein phosphatases

CATH v4.4 (2 domains)

Domain ID domain_id1d1pA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2300 — Response regulator
Domain ID domain_id1d1pB00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily2300 — Response regulator

8. Citations (2)

9. Files and Curves (10)