8cqg

Crystal Structure of a Chimeric Alpha-Amylase from Pseudoalteromonas Haloplanktis

Method: X-RAY DIFFRACTION Dmax: 81.7 Å Quality: GOOD

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

Alpha-amylase

Pseudoalteromonas haloplanktis

UniProt P29957

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 25–232 Chain A; UniProt 236–294 Chain A; UniProt 302–471 Mutation:A77V Q204L S226G T227A E228K N231T T232L G270_G271insA A272G G273S N274S V275I I276L D310N T311D D312W EDO 1,2-ETHANEDIOL × 11 CL CHLORIDE ION × 2 CA CALCIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;298 K;3 M NaCl, 0.1 M BisTris Resolution 1.74 Å R-free 0.205

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.

10 other PDB entries and 10 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name AMY_PSEHA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–209; UniProt 25–232 Author chain A; PDBConstruct 213–271; UniProt 236–294 Author chain A; PDBConstruct 280–449; UniProt 302–471

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 8cqg

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8cqg
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8cqg
Deposition date deposition_date2023-03-06
Structure title titleCrystal Structure of a Chimeric Alpha-Amylase from Pseudoalteromonas Haloplanktis
Keywords keywordsAPO, Alpha-Amylase, Hydrolase, Chimeric; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.55
Radius of gyration Rg (electron density) rg_electron22.42
Forward intensity I(0) i044710300.00
Molecular weight molecular_weight49734.0 kDa
Excluded volume excluded_volume61181 ų
Envelope volume envelope_volume69104 ų
Hydration-shell volume shell_volume25767 ų
Envelope diameter envelope_diameter81.2
Shell Rg shell_rg29.44
Envelope Rg envelope_rg22.63
Shape Rg shape_rg22.38
Total Rg total_rg23.30
Total atoms total_atoms6771
Residues n_residues447
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 dmax81.7
Rg (real space) rg_real23.53
Rg uncertainty (real space) rg_real_error0.66
I(0) (real space) i0_real4.4710e+07
I(0) uncertainty (real space) i0_real_error5.4290e+05
Rg (reciprocal space) rg_reciprocal23.54
I(0) (reciprocal space) i0_reciprocal44710000.0000
Solution quality estimate total_estimate0.7830
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.1
Skewness Skewness skewness0.366
Kurtosis Kurtosis kurtosis-0.236
Angular range angular_range— – 0.3350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7654000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.741; Stabil: 0.993; Sysdev: 1.000; Positv: 1.000; Valcen: 0.972; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id8cqgA01
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily80 — Glycosidases
Domain ID domain_id8cqgA02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily1180 — Golgi alpha-mannosidase II

8. Citations (1)

9. Files and Curves (10)