Structure of PDB 3mbz Chain A Binding Site BS01
Receptor Information
>3mbz Chain A (length=244) Species:
470
(Acinetobacter baumannii) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
HISSQQHEKAIKSYFDEAQTQGVIIIKEGKNLSTYGNALARANKEYVPAS
TFKMLNALIGLENHKATTNEIFKWDGKKRTYPMWEKDMTLGEAMALSAVP
VYQELARRTGLELMQKEVKRVNFGNTNIGTQVDNFWLVGPLKITPVQEVN
FADDLAHNRLPFKLETQEEVKKMLLIKEVNGSKIYAKSGWGMGVTPQVGW
LTGWVEQANGKKIPFSLNLEMKEGMSGSIRNEITYKSLENLGII
Ligand information
Ligand ID
MXC
InChI
InChI=1S/C16H18N4O8S/c1-16(29(26)27,7-28-15(18)25)11(14(23)24)19-13-9(6-21)5-10-4-8(12(17)22)2-3-20(10)13/h2-6,11,19H,7H2,1H3,(H2,17,22)(H2,18,25)(H,23,24)(H,26,27)/t11-,16-/m0/s1
InChIKey
WVRCRSIVCWLCEG-ZBEGNZNMSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(COC(=O)N)(C(C(=O)O)Nc1c(cc2n1ccc(c2)C(=O)N)C=O)S(=O)O
OpenEye OEToolkits 1.5.0
C[C@](COC(=O)N)([C@H](C(=O)O)Nc1c(cc2n1ccc(c2)C(=O)N)C=O)[S@](=O)O
ACDLabs 10.04
O=C(OCC(S(=O)O)(C)C(C(=O)O)Nc2c(cc1cc(ccn12)C(=O)N)C=O)N
CACTVS 3.341
C[C](COC(N)=O)([CH](Nc1n2ccc(cc2cc1C=O)C(N)=O)C(O)=O)[S](O)=O
CACTVS 3.341
C[C@](COC(N)=O)([C@@H](Nc1n2ccc(cc2cc1C=O)C(N)=O)C(O)=O)[S@@](O)=O
Formula
C16 H18 N4 O8 S
Name
(2S,3R)-2-[(7-aminocarbonyl-2-methanoyl-indolizin-3-yl)amino]-4-aminocarbonyloxy-3-methyl-3-sulfino-butanoic acid
ChEMBL
DrugBank
ZINC
ZINC000058650896
PDB chain
3mbz Chain A Residue 276 [
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
3mbz
Design, synthesis, and crystal structures of 6-alkylidene-2'-substituted penicillanic acid sulfones as potent inhibitors of Acinetobacter baumannii OXA-24 carbapenemase
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
S81 K84 Y112 S128 V130 S219 W221 R261
Binding residue
(residue number reindexed from 1)
S50 K53 Y81 S97 V99 S188 W190 R230
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=5.80,Ki=1.6uM
Enzymatic activity
Catalytic site (original residue number in PDB)
S81 K84 S128 Y133 W167 W221
Catalytic site (residue number reindexed from 1)
S50 K53 S97 Y102 W136 W190
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008658
penicillin binding
GO:0008800
beta-lactamase activity
GO:0016787
hydrolase activity
Biological Process
GO:0071555
cell wall organization
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3mbz
,
PDBe:3mbz
,
PDBj:3mbz
PDBsum
3mbz
PubMed
20822105
UniProt
Q8RLA6
[
Back to BioLiP
]