4bq8

Crystal structure of the RGMB-NEO1 complex form 3

Method: X-RAY DIFFRACTION Dmax: 90.3 Å Quality: GOOD

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

NEOGENIN

MUS MUSCULUS

UniProt P97798

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 883–1083 Fragment:FN-TYPE III DOMAINS 5 AND 6, RESIDUES 883-1083 RGM DOMAIN FAMILY MEMBER B × 1 (Q6NW40) RGM DOMAIN FAMILY MEMBER B × 1 (Q6NW40) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 4.5;0.1 M SODIUM ACETATE, PH 4.6, 0.18 M POTASSIUM ACETATE, 18 % PEG 3350 Resolution 2.80 Å R-free 0.199

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.

8 other PDB entries and 17 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NEO1_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–204; UniProt 883–1083

RGM DOMAIN FAMILY MEMBER B

HOMO SAPIENS

UniProt Q6NW40

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 50–168 Chain C; UniProt 169–410 Fragment:ECTODOMAIN, RESIDUES 50-168 Fragment:ECTODOMAIN, RESIDUES 169-410 NEOGENIN × 1 (P97798) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 4.5;0.1 M SODIUM ACETATE, PH 4.6, 0.18 M POTASSIUM ACETATE, 18 % PEG 3350 Resolution 2.80 Å R-free 0.199

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 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RGMB_HUMAN
Isoform
PDB entities 2, 3
Chains and sequence ranges Author chain B; PDBConstruct 4–122; UniProt 50–168 Author chain C; PDBConstruct 1–242; UniProt 169–410

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 4bq8

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4bq8
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4bq8
Deposition date deposition_date2013-05-30
Structure title titleCrystal structure of the RGMB-NEO1 complex form 3
Keywords keywordsCELL ADHESION; CELL ADHESION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.09
Radius of gyration Rg (electron density) rg_electron24.38
Forward intensity I(0) i028990500.00
Molecular weight molecular_weight41339.0 kDa
Excluded volume excluded_volume51730 ų
Envelope volume envelope_volume63632 ų
Hydration-shell volume shell_volume23086 ų
Envelope diameter envelope_diameter94.8
Shell Rg shell_rg29.76
Envelope Rg envelope_rg25.36
Shape Rg shape_rg24.34
Total Rg total_rg25.14
Total atoms total_atoms2909
Residues n_residues370
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 dmax90.3
Rg (real space) rg_real25.25
Rg uncertainty (real space) rg_real_error0.74
I(0) (real space) i0_real2.8990e+07
I(0) uncertainty (real space) i0_real_error4.0690e+05
Rg (reciprocal space) rg_reciprocal25.20
I(0) (reciprocal space) i0_reciprocal28990000.0000
Solution quality estimate total_estimate0.8188
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.2
Skewness Skewness skewness0.589
Kurtosis Kurtosis kurtosis0.037
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3724000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.676; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.746; Smooth: 0.866

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 3 domains

CATH v4.4 (3 domains)

Domain ID domain_id4bq8A01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins
Domain ID domain_id4bq8A02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins
Domain ID domain_id4bq8C00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology1000 — Protein Transport Mog1p; Chain A
Homologous superfamily homologous superfamily10 — Mog1/PsbP, alpha/beta/alpha sandwich

8. Citations (1)

9. Files and Curves (10)