4ebd

Conformationally Restrained North-methanocarba-2'-deoxyadenosine Corrects the Error-Prone Nature of Human DNA Polymerase Iota

Method: X-RAY DIFFRACTION Dmax: 80.3 Å Quality: GOOD

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

DNA polymerase iota

Homo sapiens

UniProt Q9UNA4

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–DNA Monomer Protein × 1 DNA 2 PDB declaration: trimeric(3) Consistent with all polymer counts Chain A; UniProt 26–445 Fragment:UNP residues 26-445 5'-D(P*AP*GP*GP*AP*CP*CP*(DOC))-3' × 1 5'-D(P*CP*TP*GP*GP*GP*TP*CP*CP*T)-3' × 1 0OJ South-methanocarba-2'-deoxyadenosine triphosphate × 1 CA CALCIUM ION × 3 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.9;277 K;20 mM Tris-HCl, pH 7.9, 5% glycerol, 10 mM 2-mercaptoethanol, 150 mM calcium chloride, 12% PEG3350, VAPOR DIFFUSION, SITTING DROP, temperature 277K Resolution 2.57 Å R-free 0.263

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.

52 other PDB entries and 53 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name POLI_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–420; UniProt 26–445

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 4ebd

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4ebd
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4ebd
Deposition date deposition_date2012-03-23
Structure title titleConformationally Restrained North-methanocarba-2'-deoxyadenosine Corrects the Error-Prone Nature of Human DNA Polymerase Iota
Keywords keywordspolymerase, TRANSFERASE-DNA complex; TRANSFERASE/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.63
Radius of gyration Rg (electron density) rg_electron23.19
Forward intensity I(0) i079913400.00
Molecular weight molecular_weight44906.0 kDa
Excluded volume excluded_volume42328 ų
Envelope volume envelope_volume71939 ų
Hydration-shell volume shell_volume25990 ų
Envelope diameter envelope_diameter87.2
Shell Rg shell_rg30.30
Envelope Rg envelope_rg23.40
Shape Rg shape_rg23.19
Total Rg total_rg23.78
Total atoms total_atoms3371
Residues n_residues391
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 dmax80.3
Rg (real space) rg_real23.58
Rg uncertainty (real space) rg_real_error0.67
I(0) (real space) i0_real7.9910e+07
I(0) uncertainty (real space) i0_real_error1.2490e+06
Rg (reciprocal space) rg_reciprocal23.60
I(0) (reciprocal space) i0_reciprocal79910000.0000
Solution quality estimate total_estimate0.7946
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.1
Skewness Skewness skewness0.318
Kurtosis Kurtosis kurtosis-0.216
Angular range angular_range— – 0.3350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha17040000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.782; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.981; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd4ebda1
Class classe — Multi-domain proteins (alpha and beta)
Fold Fold folde.8 — DNA/RNA polymerases
Superfamily Superfamily superfamilye.8.1 — DNA/RNA polymerases
Family Family familye.8.1.7 — Lesion bypass DNA polymerase (Y-family), catalytic domain
Domain ID domain_idd4ebda2
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.240 — Lesion bypass DNA polymerase (Y-family), little finger domain
Superfamily Superfamily superfamilyd.240.1 — Lesion bypass DNA polymerase (Y-family), little finger domain
Family Family familyd.240.1.1 — Lesion bypass DNA polymerase (Y-family), little finger domain

CATH v4.4 (4 domains)

Domain ID domain_id4ebdA01
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily270 — Reverse transcriptase/Diguanylate cyclase domain
Domain ID domain_id4ebdA02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology1170 — MutS, DNA mismatch repair protein, domain I
Homologous superfamily homologous superfamily60
Domain ID domain_id4ebdA03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology150 — DNA polymerase; domain 1
Homologous superfamily homologous superfamily20 — 5' to 3' exonuclease, C-terminal subdomain
Domain ID domain_id4ebdA04
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology1490 — Dna Ligase; domain 1
Homologous superfamily homologous superfamily100 — DNA polymerase, Y-family, little finger domain

8. Citations (1)

9. Files and Curves (10)