Structure of PDB 3l9w Chain A Binding Site BS02
Receptor Information
>3l9w Chain A (length=338) Species:
83333
(Escherichia coli K-12) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
GMRVIIAGFGRFGQITGRLLLSSGVKMVVLDHDPDHIETLRKFGMKVFYG
DATRMDLLESAGAAKAEVLINAIDDPQTNLQLTEMVKEHFPHLQIIARAR
DVDHYIRLRQAGVEKPERETFEGALKTGRLALESLGLGPYEARERADVFR
RFNIQMVEEMAMVGMILIIYAHPYPHHSHANKRMLEQARTLEGVEIRSLY
QLYPDFNIDIAAEQEALSRADLIVWQHPMQWYSIPPLLKLWIDKVFSHGW
AYGHGGTALHGKHLLWAVTTGGGESHFEIGAHPGFDVLSQPLQATAIYCG
LNWLPPFAMHCTFICDDETLEGQARHYKQRLLEWQEAH
Ligand information
Ligand ID
AMP
InChI
InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
UDMBCSSLTHHNCD-KQYNXXCUSA-N
SMILES
Software
SMILES
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(O)=O)[CH](O)[CH]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N
ACDLabs 12.01
O=P(O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)O)O)O)N
Formula
C10 H14 N5 O7 P
Name
ADENOSINE MONOPHOSPHATE
ChEMBL
CHEMBL752
DrugBank
DB00131
ZINC
ZINC000003860156
PDB chain
3l9w Chain A Residue 2401 [
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
3l9w
Mechanism of ligand-gated potassium efflux in bacterial pathogens.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
G408 R409 F410 D429 H430 H434 D449 A450 I471 D472 R496
Binding residue
(residue number reindexed from 1)
G10 R11 F12 D31 H32 H36 D51 A52 I73 D74 R98
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
G1107 F1113 H1118
Catalytic site (residue number reindexed from 1)
G271 F277 H282
Enzyme Commision number
?
1.6.5.2
: NAD(P)H dehydrogenase (quinone).
Gene Ontology
Molecular Function
GO:0003955
NAD(P)H dehydrogenase (quinone) activity
GO:0005515
protein binding
GO:0008753
NADPH dehydrogenase (quinone) activity
GO:0009055
electron transfer activity
GO:0010181
FMN binding
GO:0015079
potassium ion transmembrane transporter activity
GO:0016491
oxidoreductase activity
GO:0042803
protein homodimerization activity
GO:0050136
NADH:ubiquinone reductase (non-electrogenic) activity
Biological Process
GO:0006813
potassium ion transport
GO:0032414
positive regulation of ion transmembrane transporter activity
GO:0051453
regulation of intracellular pH
GO:0051454
intracellular pH elevation
GO:1901381
positive regulation of potassium ion transmembrane transport
Cellular Component
GO:0005886
plasma membrane
GO:1903103
potassium:proton antiporter complex
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3l9w
,
PDBe:3l9w
,
PDBj:3l9w
PDBsum
3l9w
PubMed
21041667
UniProt
P03819
|KEFC_ECOLI Glutathione-regulated potassium-efflux system protein KefC (Gene Name=kefC);
P0A754
[
Back to BioLiP
]