MolNFT v1 · #117520 · protein

Crystal structure of DHFR in 0% isopropanol

5EAJ · Dihydrofolate reductase: “Crystal structure of DHFR in 0% isopropanol”. X-ray diffraction, 3 ligands (FOL, CA, CL), 3 pockets (best druggability 0.76). MolNFT v1 #117520 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB: 5EAJ
Type: protein
Length: 318 residues
Chains: 2
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Dihydrofolate reductase
EC: 1.5.1.3
UniProt: C3TR70
Ligands: FOL, CA, CL
Pockets: 3 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 26% helix, 33% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
B, A	Dihydrofolate reductase (EC 1.5.1.3)	protein	159	26% helix, 33% strand	C3TR70

Ligands and binding sites

FOL · Folic acid · ligand · 2 copies · chains B, A
CA · Calcium ion · metal · chains B
CL · Chloride ion · ion · 4 copies · chains B, A

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

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	545	0.76	0.83	46	FOL, CL
2	525	0.75	0.83	43	FOL, CL
3	112	0.37	0.74	24	empty

Interfaces

1 interface between chains.

B–A · 577 Å² buried · 4 hydrogen bonds · protein-protein

Compared structures

5EAJ · Crystal structure of DHFR in 0% Isopropanol · the same entry in another collection · chain B against B, 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 C3TR70
Elsewhere: RCSB PDB 5EAJ · PDBe 5EAJ · UniProt C3TR70

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