1cag
CRYSTAL AND MOLECULAR STRUCTURE OF A COLLAGEN-LIKE PEPTIDE AT 1.9 ANGSTROM RESOLUTION
1. Protein Identity and Related Structures Protein Identity & Related Structures
No usable UniProt protein identity is available for this entry.
七张关系表仍保留该条目的 assembly 与组成信息，但缺少统一蛋白身份时，不能可靠建立跨 PDB 的同蛋白Chain接。
Assembly Composition of the Current Entry
| Assembly | Oligomeric State | 实体与Construct证据 | Mutations and Modifications | Ligands, Ions and Associated Components | Method and Experimental Conditions | Structure Quality |
|---|---|---|---|---|---|---|
| 1 | Protein homooligomer Homooligomer 蛋白 3 / DNA 0 / RNA 0 / 其他Polymer 0 PDB declaration: trimeric | Entity 1：COLLAGEN-LIKE PEPTIDE × 3 缺少 UniProt 身份时不显示参考序列区间 | Non-standard monomer：Yes (specific site not provided by mmCIF) | ACY ACETIC ACID × 6 | X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions | Resolution 1.85 Å |
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
P(r) Distance Distribution P(r) Distribution
2. Structure Basics 2. Structure Basics
| Entry ID entry_id | 1cag |
| Deposition date deposition_date | 1994-03-29 |
| Structure title title | CRYSTAL AND MOLECULAR STRUCTURE OF A COLLAGEN-LIKE PEPTIDE AT 1.9 ANGSTROM RESOLUTION |
| Keywords keywords | COLLAGEN; COLLAGEN |
| Experimental Method method | X-RAY DIFFRACTION |
3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)
| Radius of gyration Rg (Guinier) rg_guinier | 22.93 Å |
| Radius of gyration Rg (electron density) rg_electron | 24.23 Å |
| Forward intensity I(0) i0 | 1413830.00 |
| Molecular weight molecular_weight | 8340.0 kDa |
| Excluded volume excluded_volume | 10405 ų |
| Envelope volume envelope_volume | 13333 ų |
| Hydration-shell volume shell_volume | 6648 ų |
| Envelope diameter envelope_diameter | 88.8 Å |
| Shell Rg shell_rg | 23.50 Å |
| Envelope Rg envelope_rg | 25.06 Å |
| Shape Rg shape_rg | 24.22 Å |
| Total Rg total_rg | 24.12 Å |
| Total atoms total_atoms | 589 |
| Residues n_residues | 58 |
| Spherical-harmonic order n_harmonics | 20 |
| q range q_range | — – 0.5000 Å−1 |
| Data points n_points | 101 |
| Shell type shell_type | directional |
| Solvent electron density solvent_density | 0.3340 e/ų |
| Shell contrast contrast_shell | 0.0300 e/ų |
| CRYSOL version crysol_version | 4.1.3 |
4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)
| Maximum dimension Dmax dmax | 91.2 Å |
| Rg (real space) rg_real | 23.73 Å |
| Rg uncertainty (real space) rg_real_error | 1.58 Å |
| I(0) (real space) i0_real | 1.4140e+06 |
| I(0) uncertainty (real space) i0_real_error | 2.2680e+04 |
| Rg (reciprocal space) rg_reciprocal | 23.54 Å |
| I(0) (reciprocal space) i0_reciprocal | 1414000.0000 |
| Solution quality estimate total_estimate | 0.6199 |
| Solution quality rating solution_quality | REASONABLE a REASONABLE solution |
| P(r) peaks n_peaks | 2 |
| Primary peak position r_peak_primary | 11.2 Å |
| Skewness Skewness skewness | 0.697 |
| Kurtosis Kurtosis kurtosis | -0.313 |
| Angular range angular_range | — – 0.3450 Å−1 |
| Current regularization parameter α current_alpha | 0.0000 |
| Highest regularization parameter α highest_alpha | 36910.0000 |
| Real-space data points n_real_points | 66 |
| GNOM version gnom_version | 4.1.3 |
| Quality Criteria quality_criteria | AN1: 0.000; Oscil: 0.024; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.003; Smooth: 0.987 |
5. Crystallography and Experiment 5. Crystallography & Experiment
6. Entities and Polymers Entities & Polymers (3)
7. Fold Classification (SCOP + CATH) 9 domains
SCOP 2.08 (9 domains)
| Domain ID domain_id | d1caga1 |
| Class class | k — Designed proteins |
| Fold Fold fold | k.3 — Collagen-like peptides |
| Superfamily Superfamily superfamily | k.3.1 — Collagen-like peptides |
| Family Family family | k.3.1.1 — Collagen-like peptides |
| Domain ID domain_id | d1caga2 |
| Class class | l — Artifacts |
| Fold Fold fold | l.1 — Tags |
| Superfamily Superfamily superfamily | l.1.1 — Tags |
| Family Family family | l.1.1.1 — Tags |
| Domain ID domain_id | d1caga3 |
| Class class | l — Artifacts |
| Fold Fold fold | l.1 — Tags |
| Superfamily Superfamily superfamily | l.1.1 — Tags |
| Family Family family | l.1.1.1 — Tags |
| Domain ID domain_id | d1cagb1 |
| Class class | k — Designed proteins |
| Fold Fold fold | k.3 — Collagen-like peptides |
| Superfamily Superfamily superfamily | k.3.1 — Collagen-like peptides |
| Family Family family | k.3.1.1 — Collagen-like peptides |
| Domain ID domain_id | d1cagb2 |
| Class class | l — Artifacts |
| Fold Fold fold | l.1 — Tags |
| Superfamily Superfamily superfamily | l.1.1 — Tags |
| Family Family family | l.1.1.1 — Tags |
| Domain ID domain_id | d1cagb3 |
| Class class | l — Artifacts |
| Fold Fold fold | l.1 — Tags |
| Superfamily Superfamily superfamily | l.1.1 — Tags |
| Family Family family | l.1.1.1 — Tags |
| Domain ID domain_id | d1cagc1 |
| Class class | k — Designed proteins |
| Fold Fold fold | k.3 — Collagen-like peptides |
| Superfamily Superfamily superfamily | k.3.1 — Collagen-like peptides |
| Family Family family | k.3.1.1 — Collagen-like peptides |
| Domain ID domain_id | d1cagc2 |
| Class class | l — Artifacts |
| Fold Fold fold | l.1 — Tags |
| Superfamily Superfamily superfamily | l.1.1 — Tags |
| Family Family family | l.1.1.1 — Tags |
| Domain ID domain_id | d1cagc3 |
| Class class | l — Artifacts |
| Fold Fold fold | l.1 — Tags |
| Superfamily Superfamily superfamily | l.1.1 — Tags |
| Family Family family | l.1.1.1 — Tags |