Structure of PDB 6u0z Chain A Binding Site BS03
Receptor Information
>6u0z Chain A (length=266) Species:
522373
(Stenotrophomonas maltophilia K279a) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
EAPLPQLRAYTVDASWLQPMAPLQVADHTWQIGTEDLTALLVQTAEGAVL
LDGGMPQMAGHLLDNMKLRGVAPQDLRLILLSHAHADHAGPVAELKRRTG
AHVAANAETAVLLARGGSNDLHFGDGITYPPASADRIIMDGEVVTVGGIA
FTAHFMPGHTPGSTAWTWTDTRDGKPVRIAYADSLSAPGYQLKGNPRYPR
LIEDYKRSFATVRALPCDLLLTPHPGASNWNYAVGSKASAEALTCNAYAD
AAEKKFDAQLARETAG
Ligand information
Ligand ID
FRU
InChI
InChI=1S/C6H12O6/c7-1-3-4(9)5(10)6(11,2-8)12-3/h3-5,7-11H,1-2H2/t3-,4-,5+,6-/m1/s1
InChIKey
RFSUNEUAIZKAJO-ARQDHWQXSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OC1C(O)C(OC1(O)CO)CO
OpenEye OEToolkits 1.5.0
C([C@@H]1[C@H]([C@@H]([C@](O1)(CO)O)O)O)O
CACTVS 3.341
OC[CH]1O[C](O)(CO)[CH](O)[CH]1O
OpenEye OEToolkits 1.5.0
C(C1C(C(C(O1)(CO)O)O)O)O
CACTVS 3.341
OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O
Formula
C6 H12 O6
Name
beta-D-fructofuranose;
beta-D-fructose;
D-fructose;
fructose
ChEMBL
CHEMBL604608
DrugBank
ZINC
ZINC000001529270
PDB chain
6u0z Chain C Residue 2 [
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
6u0z
Crystal Structure of the metallo-beta-lactamase L1 from Stenotrophomonas maltophilia in the complex with the hydrolyzed penicillin G.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
R200 C239
Binding residue
(residue number reindexed from 1)
R178 C217
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H105 H107 D109 H110 H181 Y212 H246
Catalytic site (residue number reindexed from 1)
H83 H85 D87 H88 H159 Y190 H224
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0008800
beta-lactamase activity
Biological Process
GO:0017001
antibiotic catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6u0z
,
PDBe:6u0z
,
PDBj:6u0z
PDBsum
6u0z
PubMed
UniProt
B2FTM1
[
Back to BioLiP
]