MolNFT v1 · #38725 · protein

Crystal structure of thioredoxin mutant D10E in hexagonal (P61) space group

2H76: “Crystal structure of thioredoxin mutant D10E in hexagonal (P61) space group”. X-ray diffraction, 2 pockets (best druggability 0.37). MolNFT v1 #38725 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB: 2H76
Type: protein
Length: 215 residues
Chains: 2
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Thioredoxin
UniProt: Q2M889
Pockets: 2 · best druggability 0.37

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 26% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A	Thioredoxin	protein	108	35% helix, 27% strand	Q2M889
B	Thioredoxin	protein	107	36% helix, 24% strand	Q2M889

Ligands and binding sites

MPD · (4S)-2-methyl-2,4-pentanediol · additive · 2 copies · chains A

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

Pockets

2 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	84	0.37	0.76	20	empty
2	68	0.32	0.75	18	empty

Interfaces

1 interface between chains.

A–B · 547 Å² buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

2H76 · Crystal Structure of Thioredoxin Mutant D10E in Hexagonal (p61) Space Group · 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 Q2M889
Elsewhere: RCSB PDB 2H76 · PDBe 2H76 · UniProt Q2M889

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