MolNFT v1 · #6189 · protein

Bacteriorhodopsin-br state of the E204Q mutant at 1.7 ångström resolution

1F50: “Bacteriorhodopsin-br state of the E204Q mutant at 1.7 ångström resolution”. X-ray diffraction, 3 ligands (LI1, SQU, RET), 1 pocket (best druggability 0.78). MolNFT v1 #6189 on GenesisL1: 3D structure, binding sites and pockets in…

PDB: 1F50
Type: protein
Length: 222 residues
Chains: 1
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Bacteriorhodopsin
UniProt: P02945
Ligands: LI1, SQU, RET
Pockets: 1 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 76% helix, 5% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A	Bacteriorhodopsin	protein	222	76% helix, 5% strand	P02945

Ligands and binding sites

LI1 · 1-[2,6,10.14-tetramethyl-hexadecan-16-yl]-2-[2,10,14-trimethylhexadecan-16-yl]glycerol · ligand · 13 copies · chains A
SQU · 2,10,23-trimethyl-tetracosane · ligand · chains A
RET · Retinal · ligand · chains A

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

Pockets

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

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	98	0.78	0.98	22	RET

Modifications

Observed in the structure: 1 cofactor (retinal Schiff base).

Compared structures

1F50 · Bacteriorhodopsin-br state of the E204Q mutant at 1.7 ångström resolution · the same entry in another collection · chain A against A, TM-score 1.00
P02945 · AlphaFold monomer V2.0 prediction for bacteriorhodopsin (P02945) · a predicted model of the same protein · chain A against A, TM-score 0.99

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 P02945
Elsewhere: RCSB PDB 1F50 · PDBe 1F50 · UniProt P02945

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