6a9a

Ternary complex crystal structure of dCH with dCMP and THF

Method: X-RAY DIFFRACTION Dmax: 62.0 Å Quality: GOOD

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

Deoxycytidylate 5-hydroxymethyltransferase

Enterobacteria phage T4

UniProt P08773

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–246 Mutation:C148S, D179N IOD IODIDE ION × 2 DCM 2'-DEOXYCYTIDINE-5'-MONOPHOSPHATE × 2 THG (6S)-5,6,7,8-TETRAHYDROFOLATE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8.5;298 K;Tris-HCl pH 8.0, Sodium citrate Resolution 1.90 Å R-free 0.187

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.

5 other PDB entries and 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DCHM_BPT4
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–246; UniProt 1–246

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 6a9a

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6a9a
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id6a9a
Deposition date deposition_date2018-07-12
Structure title titleTernary complex crystal structure of dCH with dCMP and THF
Keywords keywordspyrimidine hydroxymethylase, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.66
Radius of gyration Rg (electron density) rg_electron18.69
Forward intensity I(0) i015423100.00
Molecular weight molecular_weight29332.0 kDa
Excluded volume excluded_volume36502 ų
Envelope volume envelope_volume41605 ų
Hydration-shell volume shell_volume18766 ų
Envelope diameter envelope_diameter64.2
Shell Rg shell_rg24.79
Envelope Rg envelope_rg19.02
Shape Rg shape_rg18.65
Total Rg total_rg19.70
Total atoms total_atoms2062
Residues n_residues246
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 dmax62.0
Rg (real space) rg_real19.58
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real1.5420e+07
I(0) uncertainty (real space) i0_real_error2.0000e+05
Rg (reciprocal space) rg_reciprocal19.59
I(0) (reciprocal space) i0_reciprocal15420000.0000
Solution quality estimate total_estimate0.8218
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary23.6
Skewness Skewness skewness0.236
Kurtosis Kurtosis kurtosis-0.412
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2916000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.894; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd6a9aa_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.117 — Thymidylate synthase/dCMP hydroxymethylase
Superfamily Superfamily superfamilyd.117.1 — Thymidylate synthase/dCMP hydroxymethylase
Family Family familyd.117.1.1 — Thymidylate synthase/dCMP hydroxymethylase

CATH v4.4 (1 domains)

Domain ID domain_id6a9aA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology572 — Thymidylate Synthase; Chain A
Homologous superfamily homologous superfamily10 — Thymidylate synthase/dCMP hydroxymethylase domain

8. Citations (1)

9. Files and Curves (10)