MolNFT v1 · #38719 · protein

Crystal structure of thioredoxin mutant D9E in hexagonal (P61) space group

2H70: “Crystal structure of thioredoxin mutant D9E in hexagonal (P61) space group”. X-ray diffraction, 3 pockets (best druggability 0.41). MolNFT v1 #38719 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB: 2H70
Type: protein
Length: 214 residues
Chains: 2
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Thioredoxin
UniProt: Q2M889
Pockets: 3 · best druggability 0.41

Structure

x-ray diffraction · 1 distinct chain · 36% helix, 26% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A, B	Thioredoxin	protein	107	36% helix, 26% strand	Q2M889

Ligands and binding sites

MPD · (4S)-2-methyl-2,4-pentanediol · additive · 3 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	93	0.41	0.78	20	empty
2	73	0.35	0.76	14	empty
3	74	0.32	0.74	18	MPD

Interfaces

1 interface between chains.

A–B · 528 Å² buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

2H70 · Crystal Structure of Thioredoxin Mutant D9E 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 2H70 · PDBe 2H70 · UniProt Q2M889

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