1qg1

GROWTH FACTOR RECEPTOR BINDING PROTEIN SH2 DOMAIN COMPLEXED WITH AN SHC-DERIVED PEPTIDE

Method: SOLUTION NMR Dmax: 57.1 Å Quality: REASONABLE

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

PROTEIN (GROWTH FACTOR RECEPTOR BINDING PROTEIN)

Homo sapiens

UniProt P62993

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 E; UniProt 58–159 Fragment:SH2 PROTEIN (SHC-DERIVED PEPTIDE) × 1 (P29353) SOLUTION NMR NMR measurement conditions:pH 6.3;301 K 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.

50 other PDB entries and 103 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name GRB2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain E; PDBConstruct 3–104; UniProt 58–159

PROTEIN (SHC-DERIVED PEPTIDE)

OrganismNot specified

UniProt P29353

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 I; UniProt 423–435 Fragment:423-435 Non-standard monomer:Yes (specific site not provided by mmCIF) PROTEIN (GROWTH FACTOR RECEPTOR BINDING PROTEIN) × 1 (P62993) SOLUTION NMR NMR measurement conditions:pH 6.3;301 K 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.

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

View Construct and Data Evidence
UniProt name SHC1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain I; PDBConstruct 1–13; UniProt 423–435

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 1qg1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1qg1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1qg1
Deposition date deposition_date1999-04-19
Structure title titleGROWTH FACTOR RECEPTOR BINDING PROTEIN SH2 DOMAIN COMPLEXED WITH AN SHC-DERIVED PEPTIDE
Keywords keywordsSIGNAL TRANSDUCTION, SH2 DOMAIN, PHOSPHOTYROSYL PEPTIDE, COMPLEX (SIGNAL TRANSDUCTION-PEPTIDE), HORMONE-GROWTH FACTOR COMPLEX; HORMONE/GROWTH FACTOR
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier15.22
Radius of gyration Rg (electron density) rg_electron13.64
Forward intensity I(0) i03847820.00
Molecular weight molecular_weight13582.0 kDa
Excluded volume excluded_volume16879 ų
Envelope volume envelope_volume18911 ų
Hydration-shell volume shell_volume11725 ų
Envelope diameter envelope_diameter52.9
Shell Rg shell_rg19.52
Envelope Rg envelope_rg14.42
Shape Rg shape_rg13.60
Total Rg total_rg14.99
Total atoms total_atoms1886
Residues n_residues116
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 dmax57.1
Rg (real space) rg_real15.15
Rg uncertainty (real space) rg_real_error0.50
I(0) (real space) i0_real3.8480e+06
I(0) uncertainty (real space) i0_real_error4.7750e+04
Rg (reciprocal space) rg_reciprocal15.16
I(0) (reciprocal space) i0_reciprocal3848000.0000
Solution quality estimate total_estimate0.7344
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary19.5
Skewness Skewness skewness0.255
Kurtosis Kurtosis kurtosis-0.077
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha779900.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.535; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.938; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1qg1e1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.93 — SH2-like
Superfamily Superfamily superfamilyd.93.1 — SH2 domain
Family Family familyd.93.1.1 — SH2 domain
Domain ID domain_idd1qg1e2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (1 domains)

Domain ID domain_id1qg1E00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology505 — SHC Adaptor Protein
Homologous superfamily homologous superfamily10 — SH2 domain

8. Citations (1)

9. Files and Curves (10)