MolNFT v1 · #93521 · protein

Crystal structure of ferredoxin reductase, BPHA4 E175C/T176R/Q177G mutant (reduced form)

4H4W · Biphenyl dioxygenase ferredoxin reductase subunit: “Crystal structure of ferredoxin reductase, BPHA4 E175C/T176R/Q177G mutant (reduced form)”. X-ray diffraction, 2 ligands (FAD, NAP), 2 pockets (best druggability 0.83). MolNFT v1…

PDB: 4H4W
Type: protein
Length: 399 residues
Chains: 1
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Biphenyl dioxygenase ferredoxin reductase subunit
EC: 1.18.1.3
UniProt: E7FJB9
Ligands: FAD, NAP
Pockets: 2 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 27% helix, 29% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A	Biphenyl dioxygenase ferredoxin reductase subunit (EC 1.18.1.3)	protein	399	27% helix, 29% strand	E7FJB9

Ligands and binding sites

FAD · Flavin-adenine dinucleotide · ligand · chains A
NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · chains A
FMT · Formic acid · additive · 5 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, 1 with a druggability of 0.5 or more.

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	782	0.83	0.86	87	FAD, NAP
2	110	0.47	0.79	16	empty

Compared structures

4H4W · Crystal Structure of Ferredoxin reductase, BphA4 E175C/T176R/Q177G mutant (reduced form) · 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 E7FJB9
Elsewhere: RCSB PDB 4H4W · PDBe 4H4W · UniProt E7FJB9

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