Structure of PDB 2xnj Chain B Binding Site BS04
Receptor Information
>2xnj Chain B (length=250) Species:
562
(Escherichia coli) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
ADWVTGKVTKVQNWTDALFSLTVHAPVLPFTAGQFTKLGLEIDGERVQRA
YSYVNSPDNPDLEFYLVTVVYTNDAGEVVKGKLSPRLAALKPGDEVQVVS
EAAGFFVLDEVPHCETLWMLATGTAIGPYLSILRLGKDLDRFKNLVLVHA
ARYAADLSYLPLMQELEKRYEGKLRIQTVVSRETAAGSLTGRIPALIESG
ELESTIGLPMNKETSHVMLCGNPQMVRDTQQLLKETRQMTKHGHMTAEHY
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2xnj Chain B Residue 1264 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
2xnj
Swapping Fad Binding Motifs between Plastidic and Bacterial Ferredoxin-Nadp(H) Reductases.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
E111 H243
Binding residue
(residue number reindexed from 1)
E110 H242
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F36 Y52 S53 C221 E254 Y256
Catalytic site (residue number reindexed from 1)
F35 Y51 S52 C220 E248 Y250
Enzyme Commision number
1.18.1.2
: ferredoxin--NADP(+) reductase.
1.19.1.1
: flavodoxin--NADP(+) reductase.
Gene Ontology
Molecular Function
GO:0004324
ferredoxin-NADP+ reductase activity
GO:0016491
oxidoreductase activity
View graph for
Molecular Function
External links
PDB
RCSB:2xnj
,
PDBe:2xnj
,
PDBj:2xnj
PDBsum
2xnj
PubMed
21306142
UniProt
P28861
|FENR_ECOLI Flavodoxin/ferredoxin--NADP reductase (Gene Name=fpr)
[
Back to BioLiP
]