2c7r

HhaI DNA methyltransferase (T250G mutant) complex with oligonucleotide containing 2-aminopurine as a target base (GPGC:GMGC) and SAH

Method: X-RAY DIFFRACTION Dmax: 76.2 Å Quality: GOOD

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

MODIFICATION METHYLASE HHAI

HAEMOPHILUS HAEMOLYTICUS

UniProt P05102

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 1–327 Mutation:YES 5'-D(*G*GP*AP*TP*GP*(5CM)*GP*CP*TP*GP*AP*C)-3' × 1 5'-D(*G*TP*CP*AP*GP*(2PR)*GP*CP*AP*TP*CP*C)-3' × 1 SAH S-ADENOSYL-L-HOMOCYSTEINE × 1 SO4 SULFATE ION × 7 GOL GLYCEROL × 5 X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.6;50 MM NA CITRATE PH 5.6, 1.7 M AMMONIUM SULFATE, 5 % GLUCOSE Resolution 1.90 Å R-free 0.217

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.

30 other PDB entries and 31 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MTH1_HAEHA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–327; UniProt 1–327

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 2c7r

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2c7r
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2c7r
Deposition date deposition_date2005-11-27
Structure title titleHhaI DNA methyltransferase (T250G mutant) complex with oligonucleotide containing 2-aminopurine as a target base (GPGC:GMGC) and SAH
Keywords keywordsBASE FLIPPING, RESTRICTION SYSTEM, TRANSFERASE-DNA COMPLEX, TRANSFERASE; TRANSFERASE/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.96
Radius of gyration Rg (electron density) rg_electron20.85
Forward intensity I(0) i044450800.00
Molecular weight molecular_weight45984.0 kDa
Excluded volume excluded_volume55014 ų
Envelope volume envelope_volume63876 ų
Hydration-shell volume shell_volume24978 ų
Envelope diameter envelope_diameter79.3
Shell Rg shell_rg28.12
Envelope Rg envelope_rg21.26
Shape Rg shape_rg20.80
Total Rg total_rg21.75
Total atoms total_atoms3191
Residues n_residues349
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 dmax76.2
Rg (real space) rg_real21.84
Rg uncertainty (real space) rg_real_error0.47
I(0) (real space) i0_real4.4450e+07
I(0) uncertainty (real space) i0_real_error6.0230e+05
Rg (reciprocal space) rg_reciprocal21.86
I(0) (reciprocal space) i0_reciprocal44450000.0000
Solution quality estimate total_estimate0.8607
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.3
Skewness Skewness skewness0.239
Kurtosis Kurtosis kurtosis-0.311
Angular range angular_range— – 0.3600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7776000.0000
Real-space data points n_real_points68
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.734; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.989; Smooth: 0.994

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2c7ra_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.66 — S-adenosyl-L-methionine-dependent methyltransferases
Superfamily Superfamily superfamilyc.66.1 — S-adenosyl-L-methionine-dependent methyltransferases
Family Family familyc.66.1.26 — C5 cytosine-specific DNA methylase, DCM

CATH v4.4 (2 domains)

Domain ID domain_id2c7rA01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily150 — Vaccinia Virus protein VP39
Domain ID domain_id2c7rA02
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology120 — DNA Methylase; Chain A, domain 2
Homologous superfamily homologous superfamily10 — DNA Methylase, subunit A, domain 2

8. Citations (1)

9. Files and Curves (10)