Structure of PDB 3fi0 Chain F Binding Site BS02
Receptor Information
>3fi0 Chain F (length=296) Species:
1422
(Geobacillus stearothermophilus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MKTIFSGIQIGNYIGALRQFVELQHEYNCYFCIVDQHAITVWQDPHELRQ
NIRRLAALYLAVGIDPTQATLFIQSEVPAHAQAAWMLQCIVYIGELERMT
QVSAGLLTYPPLMAADILLYNTDIVPVGEDQKQHIELTRDLAERFNKRFT
IPEARIPKVGARIMSLVDPTKKMSKSDPNPKAYITLLDDAKTIEKKIKSS
EGTIRYGISNLLNIYSTLSGQSIEELERQYEGKGYGVFKADLAQVVIETL
RPIQERYHHWMESEELDRVLDEGAEKANRVASEMVRKMEQAMGLGR
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
3fi0 Chain F Residue 1003 [
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
3fi0
Independent saturation of three TrpRS subsites generates a partially assembled state similar to those observed in molecular simulations.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
G17 N18 I183
Binding residue
(residue number reindexed from 1)
G11 N12 I163
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K192 K195
Catalytic site (residue number reindexed from 1)
K172 K175
Enzyme Commision number
6.1.1.2
: tryptophan--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004830
tryptophan-tRNA ligase activity
GO:0005524
ATP binding
Biological Process
GO:0006412
translation
GO:0006418
tRNA aminoacylation for protein translation
GO:0006436
tryptophanyl-tRNA aminoacylation
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3fi0
,
PDBe:3fi0
,
PDBj:3fi0
PDBsum
3fi0
PubMed
19174517
UniProt
P00953
|SYW_GEOSE Tryptophan--tRNA ligase (Gene Name=trpS)
[
Back to BioLiP
]