Structure of PDB 1fws Chain A Binding Site BS01
Receptor Information
>1fws Chain A (length=256) Species:
63363
(Aquifex aeolicus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
EKFLVIAGPCAIESEELLLKVGEEIKRLSEKFKEVEFVFKSSFDKANRSS
IHSFRGHGLEYGVKALRKVKEEFGLKITTDIHESWQAEPVAEVADIIQIP
AFLCRQTDLLLAAAKTGRAVNVKKGQFLAPWDTKNVVEKLKFGGAKEIYL
TERGTTFGYNNLVVDFRSLPIMKQWAKVIYDATHSVQLPGGMREFIFPLI
RAAVAVGCDGVFMETHPEPEKALSDASTQLPLSQLEGIIEAILEIREVAS
KYYETI
Ligand information
Ligand ID
PEP
InChI
InChI=1S/C3H5O6P/c1-2(3(4)5)9-10(6,7)8/h1H2,(H,4,5)(H2,6,7,8)
InChIKey
DTBNBXWJWCWCIK-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C=C(C(=O)O)OP(=O)(O)O
CACTVS 3.341
OC(=O)C(=C)O[P](O)(O)=O
ACDLabs 10.04
O=C(O)C(\OP(=O)(O)O)=C
Formula
C3 H5 O6 P
Name
PHOSPHOENOLPYRUVATE
ChEMBL
CHEMBL1235228
DrugBank
DB01819
ZINC
ZINC000003870145
PDB chain
1fws Chain A Residue 1268 [
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
1fws
Electronic structure of the metal center in the Cd(2+), Zn(2+), and Cu(2+) substituted forms of KDO8P synthase: implications for catalysis.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
K1041 K1046 Q1099 P1101 A1102 K1124 R1154 H1185
Binding residue
(residue number reindexed from 1)
K40 K45 Q98 P100 A101 K123 R153 H184
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.5.1.55
: 3-deoxy-8-phosphooctulonate synthase.
Gene Ontology
Molecular Function
GO:0008676
3-deoxy-8-phosphooctulonate synthase activity
GO:0016740
transferase activity
Biological Process
GO:0009058
biosynthetic process
GO:0009103
lipopolysaccharide biosynthetic process
GO:0019294
keto-3-deoxy-D-manno-octulosonic acid biosynthetic process
GO:0046364
monosaccharide biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1fws
,
PDBe:1fws
,
PDBj:1fws
PDBsum
1fws
PubMed
19228070
UniProt
O66496
|KDSA_AQUAE 2-dehydro-3-deoxyphosphooctonate aldolase (Gene Name=kdsA)
[
Back to BioLiP
]