Research workbench

Crystal structure of V44G cp rubredoxin

Analyse Crystal structure of V44G cp rubredoxin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB: 1T9O
Type: protein
Length: 159 residues
Chains: 3
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Rubredoxin
UniProt: P00268
Ligands: FE
Pockets: 1 · best druggability 0.40

Structure

x-ray diffraction · 1 distinct chain · 17% helix, 23% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A, B, C	Rubredoxin	protein	53	17% helix, 23% strand	P00268

Ligands and binding sites

FE · Fe (III) ion · metal · 3 copies · chains A, B, C

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

Pockets

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

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	50	0.40	0.82	17	empty

Interfaces

3 interfaces between chains.

A–C · 385 Å² buried · 8 hydrogen bonds · protein-protein
B–C · 332 Å² buried · 3 hydrogen bonds · protein-protein
A–B · 70 Å² buried · 0 hydrogen bonds · protein-protein

Compared structures

1T9O · Crystal Structure of V44G Cp Rubredoxin · the same entry in another collection · chain A against A, TM-score 1.00
P00268 · AlphaFold monomer V2.0 prediction for rubredoxin (P00268) · a predicted model of the same protein · chain A against A, TM-score 0.98

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 P00268
Elsewhere: RCSB PDB 1T9O · PDBe 1T9O · UniProt P00268

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.