3bhd

Crystal structure of human thiamine triphosphatase (THTPA)

Method: X-RAY DIFFRACTION
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1. Protein Identity and Related Structures Protein Identity & Related Structures

Thiamine triphosphatase

Homo sapiens

UniProt Q9BU02

State in the Current Structure

Assembly Physical composition Protein state Molecular copy count Associated components Data consistency
1 Protein monomer Monomer Protein 1 SULFATE ION × 1 CHLORIDE ION × 2 CITRIC ACID × 1 water × 1 Consistent with protein count
2 Protein monomer Monomer Protein 1 CITRIC ACID × 2 SODIUM ION × 1 GLYCEROL × 5 water × 1 Consistent with protein count

Other States of the Same Protein in the Database

View Construct and Data Evidence
UniProt name THTPA_HUMAN
Isoform —
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 20–234; UniProt 1–215 Author chain B; PDBConstruct 20–234; UniProt 1–215

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.

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2. Structure Basics 2. Structure Basics

Entry ID entry_id3bhd
Deposition date deposition_date2007-11-28
Structure title titleCrystal structure of human thiamine triphosphatase (THTPA)
Keywords keywordsHydrolase, Structural Genomics Consortium, Phosphatase, CYTH domain, SGC; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION
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3. Official assembly/model SAXS Official SAXS Profiles

This page reads only the latest assembly calculations. Every curve maps to an explicit PDB entry, official biological assembly and coordinate model.

3bhd__assembly_1__model_1

Assembly 1 · Model 1 · CRYSOL 4.1.3-1-20251215 (887e7ef)

Download this curve (.dat)

3bhd__assembly_1__model_1 | I(q)

10-2 10-1 105 106 107 q (1/Angstrom) I(q)
100 plotted points; both axes use logarithmic scales.

3bhd__assembly_1__model_1 | P(r) · Pending

The new assembly/model P(r) has not been calculated yet This placeholder does not display legacy data r (Angstrom) P(r)
P(r) will be calculated and displayed separately for the same assembly/model.
Rg(Guinier)18.12 Å
Rg (electron density)17.08 Å
Total Rg18.08 Å
Atom count1670
Residues208
Excluded volume29718 ų
Maximum q0.500 Å⁻¹
Assembly Model Structure unit Oligomeric description Status CRYSOL Actions
1 1 3bhd__assembly_1__model_1 monomeric (1) Success 4.1.3-1-20251215 (887e7ef) View Download
2 1 3bhd__assembly_2__model_1 monomeric (1) Success 4.1.3-1-20251215 (887e7ef) View Download
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4. Crystallography and Experiment 4. Crystallography & Experiment

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5. Entities and Polymers Entities & Polymers (7)

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6. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3bhda_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.63 — CYTH-like phosphatases
Superfamily Superfamily superfamilyd.63.1 — CYTH-like phosphatases
Family Family familyd.63.1.2 — CYTH domain
Domain ID domain_idd3bhdb_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.63 — CYTH-like phosphatases
Superfamily Superfamily superfamilyd.63.1 — CYTH-like phosphatases
Family Family familyd.63.1.2 — CYTH domain

CATH v4.4 (2 domains)

Domain ID domain_id3bhdA00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology320 — Hypothetical Protein Pfu-838710-001
Homologous superfamily homologous superfamily10 — Hypothetical Protein Pfu-838710-001
Domain ID domain_id3bhdB00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology320 — Hypothetical Protein Pfu-838710-001
Homologous superfamily homologous superfamily10 — Hypothetical Protein Pfu-838710-001
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7. Citations (1)