Structure of PDB 3m83 Chain D Binding Site BS03
Receptor Information
>3m83 Chain D (length=324) Species:
2336
(Thermotoga maritima) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
HMAFFDLPLEELKKYRPERYEEKDFDEFWEETLAESEKFPLDPVFERMES
HLKTVEAYDVTFSGYRGQRIKGWLLVPKLEEEKLPCVVQYIGYNGGRGFP
HDWLFWPSMGYICFVMDTRGQGSGWLKGDTPDYPEGPVDPQYPGFMTRGI
LDPRTYYYRRVFTDAVRAVEAAASFPQVDQERIVIAGGSQGGGIALAVSA
LSKKAKALLCDVPFLCHFRRAVQLVDTHPYAEITNFLKTHRDKEEIVFRT
LSYFDGVNFAARAKIPALFSVGLMDNICPPSTVFAAYNYYAGPKEIRIYP
YNNHEGGGSFQAVEQVKFLKKLFE
Ligand information
Ligand ID
ACT
InChI
InChI=1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)/p-1
InChIKey
QTBSBXVTEAMEQO-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
[O-]C(=O)C
OpenEye OEToolkits 1.5.0
CC(=O)[O-]
CACTVS 3.341
CC([O-])=O
Formula
C2 H3 O2
Name
ACETATE ION
ChEMBL
DrugBank
DB14511
ZINC
PDB chain
3m83 Chain D Residue 410 [
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
3m83
Functional and structural characterization of a thermostable acetyl esterase from Thermotoga maritima.
Resolution
2.12 Å
Binding residue
(original residue number in PDB)
Q140 P142 G143 F144 R147
Binding residue
(residue number reindexed from 1)
Q141 P143 G144 F145 R148
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
S188 Q189 D274 H303
Catalytic site (residue number reindexed from 1)
S189 Q190 D275 H304
Enzyme Commision number
3.1.1.41
: cephalosporin-C deacetylase.
3.1.1.72
: acetylxylan esterase.
Gene Ontology
Molecular Function
GO:0005509
calcium ion binding
GO:0016788
hydrolase activity, acting on ester bonds
GO:0046555
acetylxylan esterase activity
GO:0046872
metal ion binding
GO:0047739
cephalosporin-C deacetylase activity
GO:0052689
carboxylic ester hydrolase activity
Biological Process
GO:0005976
polysaccharide metabolic process
GO:0030245
cellulose catabolic process
GO:0045491
xylan metabolic process
GO:1901266
cephalosporin C metabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3m83
,
PDBe:3m83
,
PDBj:3m83
PDBsum
3m83
PubMed
22411095
UniProt
Q9WXT2
|CAH_THEMA Cephalosporin-C deacetylase (Gene Name=axeA)
[
Back to BioLiP
]