4zzz

Structure of human PARP1 catalytic domain bound to an isoindolinone inhibitor

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

POLY [ADP-RIBOSE] POLYMERASE 1

HOMO SAPIENS

UniProt P09874

State in the Current Structure

Assembly Physical composition Protein state Molecular copy count Associated components Data consistency
1 Protein homooligomer Homooligomer Protein 2 SULFATE ION × 4 GLYCEROL × 3 2-(3-methoxypropyl)-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamide × 2 water × 2 Consistent with protein count

Other States of the Same Protein in the Database

View Construct and Data Evidence
UniProt name PARP1_HUMAN
Isoform —
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–362; UniProt 655–1014 Author chain B; PDBConstruct 3–362; UniProt 655–1014

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_id4zzz
Deposition date deposition_date2015-04-15
Structure title titleStructure of human PARP1 catalytic domain bound to an isoindolinone inhibitor
Keywords keywordsTRANSFERASE, HUMAN PARP1, ARTD1; TRANSFERASE
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.

4zzz__assembly_1__model_1

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

Download this curve (.dat)

4zzz__assembly_1__model_1 | I(q)

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

4zzz__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)29.59 Å
Rg (electron density)29.17 Å
Total Rg29.97 Å
Atom count5530
Residues692
Excluded volume99268 ų
Maximum q0.500 Å⁻¹
Assembly Model Structure unit Oligomeric description Status CRYSOL Actions
1 1 4zzz__assembly_1__model_1 dimeric (2) 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 (5)

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6. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd4zzzb1
Class classa — All alpha proteins
Fold Fold folda.41 — Domain of poly(ADP-ribose) polymerase
Superfamily Superfamily superfamilya.41.1 — Domain of poly(ADP-ribose) polymerase
Family Family familya.41.1.0 — automated matches
Domain ID domain_idd4zzzb2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.166 — ADP-ribosylation
Superfamily Superfamily superfamilyd.166.1 — ADP-ribosylation
Family Family familyd.166.1.0 — automated matches

CATH v4.4 (4 domains)

Domain ID domain_id4zzzA01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology142 — Poly(ADP-ribose) Polymerase; domain 1
Homologous superfamily homologous superfamily10 — Poly(ADP-ribose) polymerase, regulatory domain
Domain ID domain_id4zzzA02
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology228 — Phosphoenolpyruvate Carboxykinase; domain 3
Homologous superfamily homologous superfamily10 —
Domain ID domain_id4zzzB01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology142 — Poly(ADP-ribose) Polymerase; domain 1
Homologous superfamily homologous superfamily10 — Poly(ADP-ribose) polymerase, regulatory domain
Domain ID domain_id4zzzB02
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology228 — Phosphoenolpyruvate Carboxykinase; domain 3
Homologous superfamily homologous superfamily10 —
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7. Citations (1)