Structure of PDB 3deq Chain A Binding Site BS01
Receptor Information
>3deq Chain A (length=341) Species:
243274
(Thermotoga maritima MSB8) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
RIVNVKLSLKRYEYEKPFHITGSVSSESRNVEVEIVLESGVKGYGEASPS
FRVNGERVEALLAIENAVREMITGIDVRNYARIFEITDRLFGFPSLKAAV
QFATLDALSQELGTQVCYLLGGKRDEIETDKTVGIDTVENRVKEAKKIFE
EGFRVIKIKVGENLKEDIEAVEEIAKVTRGAKYIVDANMGYTQKEAVEFA
RAVYQKGIDIAVYEQPVRREDIEGLKFVRFHSPFPVAADESARTKFDVMR
LVKEEAVDYVNIKLMKSGISDALAIVEIAESSGLKLMIGCMGESSLGINQ
SVHFALGTGAFEFHDLDSHLMLKEEVFRGKFIQDGPRMRVK
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
3deq Chain A Residue 401 [
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
3deq
Discovery of a dipeptide epimerase enzymatic function guided by homology modeling and virtual screening.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
D188 E216 D241
Binding residue
(residue number reindexed from 1)
D186 E214 D239
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F20 T134 K159 K161 D188 E216 D241 E242 S243 K265 G291 C292 M293 H316 D317 L318
Catalytic site (residue number reindexed from 1)
F18 T132 K157 K159 D186 E214 D239 E240 S241 K263 G289 C290 M291 H314 D315 L316
Enzyme Commision number
5.1.1.20
: L-Ala-D/L-Glu epimerase.
Gene Ontology
Molecular Function
GO:0016853
isomerase activity
GO:0016854
racemase and epimerase activity
GO:0016855
racemase and epimerase activity, acting on amino acids and derivatives
GO:0046872
metal ion binding
GO:0103031
L-Ala-D/L-Glu epimerase activity
Biological Process
GO:0016998
cell wall macromolecule catabolic process
GO:0071555
cell wall organization
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3deq
,
PDBe:3deq
,
PDBj:3deq
PDBsum
3deq
PubMed
19000819
UniProt
Q9WXM1
|AEEP_THEMA L-Ala-D/L-Glu epimerase (Gene Name=TM_0006)
[
Back to BioLiP
]