1rlp

TWO BINDING ORIENTATIONS FOR PEPTIDES TO SRC SH3 DOMAIN: DEVELOPMENT OF A GENERAL MODEL FOR SH3-LIGAND INTERACTIONS

Method: SOLUTION NMR Dmax: 41.5 Å Quality: GOOD

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

C-SRC TYROSINE KINASE SH3 DOMAIN

Gallus gallus

UniProt P00523

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 76–139 Not recorded PROLINE-RICH LIGAND RLP2 (RALPPLPRY) × 1 SOLUTION NMR mmCIF provides none of the parsed experimental conditions Resolution not provided

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.

133 other PDB entries and 236 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SRC_CHICK
Isoform
PDB entities 1
Chains and sequence ranges Author chain C; PDBConstruct 1–64; UniProt 76–139

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 1rlp

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1rlp
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1rlp
Deposition date deposition_date1994-10-10
Structure title titleTWO BINDING ORIENTATIONS FOR PEPTIDES TO SRC SH3 DOMAIN: DEVELOPMENT OF A GENERAL MODEL FOR SH3-LIGAND INTERACTIONS
Keywords keywordsCOMPLEX (SIGNAL TRANSDUCTION-PEPTIDE), COMPLEX (SIGNAL TRANSDUCTION-PEPTIDE) complex; COMPLEX (SIGNAL TRANSDUCTION/PEPTIDE)
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier11.61
Radius of gyration Rg (electron density) rg_electron11.29
Forward intensity I(0) i0196402000.00
Molecular weight molecular_weight119250.0 kDa
Excluded volume excluded_volume149530 ų
Envelope volume envelope_volume18889 ų
Hydration-shell volume shell_volume11787 ų
Envelope diameter envelope_diameter46.1
Shell Rg shell_rg19.37
Envelope Rg envelope_rg14.16
Shape Rg shape_rg11.24
Total Rg total_rg11.73
Total atoms total_atoms16560
Residues n_residues1040
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 dmax41.5
Rg (real space) rg_real11.56
Rg uncertainty (real space) rg_real_error0.30
I(0) (real space) i0_real1.9640e+08
I(0) uncertainty (real space) i0_real_error1.9600e+06
Rg (reciprocal space) rg_reciprocal11.56
I(0) (reciprocal space) i0_reciprocal196400000.0000
Solution quality estimate total_estimate0.7506
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary14.7
Skewness Skewness skewness0.244
Kurtosis Kurtosis kurtosis-0.001
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha158900.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.587; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.992; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1rlpc_
Class classb — All beta proteins
Fold Fold foldb.34 — SH3-like barrel
Superfamily Superfamily superfamilyb.34.2 — SH3-domain
Family Family familyb.34.2.1 — SH3-domain

CATH v4.4 (1 domains)

Domain ID domain_id1rlpC00
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology30 — SH3 type barrels.
Homologous superfamily homologous superfamily40 — SH3 Domains

8. Citations (3)

9. Files and Curves (10)