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Human transthyretin (ttr) complexed with 3-(9H-fluoren-9- YLIDENEAMINOOXY)PROPANOIC acid in a dual binding mode

Analyse Human transthyretin (ttr) complexed with 3-(9H-fluoren-9… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB: 4TQI
Type: protein
Length: 232 residues
Chains: 2
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Transthyretin
UniProt: P02766
Ligands: 6BD
Pockets: 3 · best druggability 0.35

Structure

x-ray diffraction · 1 distinct chain · 6% helix, 51% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A, B	Transthyretin	protein	116	6% helix, 51% strand	P02766

Ligands and binding sites

6BD · (2S)-3-[(9H-fluoren-9-ylideneamino)oxy]-2-methylpropanoic acid · ligand · 2 copies · chains A, B
GOL · Glycerol · additive · 2 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	75	0.35	0.76	16	empty
2	60	0.34	0.77	14	empty
3	52	0.30	0.76	11	GOL

Interfaces

1 interface between chains.

A–B · 925 Å² buried · 19 hydrogen bonds · protein-protein

Compared structures

4TQI · Human transthyretin (TTR) complexed with 3-(9H-fluoren-9-ylideneaminooxy)propanoic acid… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
Every structure of UniProt P02766
Elsewhere: RCSB PDB 4TQI · PDBe 4TQI · UniProt P02766

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