Structure of PDB 2ntb Chain B Binding Site BS03
Receptor Information
>2ntb Chain B (length=342) Species:
198628
(Dickeya dadantii 3937) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
ATTYNAVVSKSSSDGKTFKTIADAIASAPAGSTPFVILIKNGVYNERLTI
TRNNLHLKGESRNGAVIAAATAAGTLKSDGSKWGTAGSSTITISAKDFSA
QSLTIRNDFDFPANQAKSDSDSSKIKDTQAVALYVTKSGDRAYFKDVSLV
GYQDTLYVSGGRSFFSDCRISGTVDFIFGDGTALFNNCDLVSRYRADVKS
GNVSGYLTAPSTNINQKYGLVITNSRVIRESDSVPAKSYGLGRPWHPTTT
FSDGRYADPNAIGQTVFLNTSMDNHIYGWDKMSGKDKNGNTIWFNPEDSR
FFEYKSYGAGATVSKDRRQLTDAQAAEYTQSKVLGDWTPTLP
Ligand information
Ligand ID
ADA
InChI
InChI=1S/C6H10O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,6-9,12H,(H,10,11)/t1-,2+,3+,4-,6-/m0/s1
InChIKey
AEMOLEFTQBMNLQ-BKBMJHBISA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1(C(C(OC(C1O)O)C(=O)O)O)O
CACTVS 3.341
O[CH]1O[CH]([CH](O)[CH](O)[CH]1O)C(O)=O
CACTVS 3.341
O[C@H]1O[C@@H]([C@H](O)[C@H](O)[C@H]1O)C(O)=O
ACDLabs 10.04
O=C(O)C1OC(O)C(O)C(O)C1O
OpenEye OEToolkits 1.5.0
[C@@H]1([C@H]([C@H](O[C@@H]([C@@H]1O)O)C(=O)O)O)O
Formula
C6 H10 O7
Name
alpha-D-galactopyranuronic acid;
alpha-D-galacturonic acid;
D-galacturonic acid;
galacturonic acid;
ALPHA D-GALACTURONIC ACID
ChEMBL
DrugBank
DB03511
ZINC
ZINC000004228259
PDB chain
2ntb Chain D Residue 5 [
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
2ntb
Molecular basis of the activity of the phytopathogen pectin methylesterase.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
T109 A110 P271 T272
Binding residue
(residue number reindexed from 1)
T85 A86 P247 T248
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q153 Q177 D178 D199 R267
Catalytic site (residue number reindexed from 1)
Q129 Q153 D154 D175 R243
Enzyme Commision number
3.1.1.11
: pectinesterase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0030599
pectinesterase activity
GO:0052689
carboxylic ester hydrolase activity
Biological Process
GO:0042545
cell wall modification
GO:0045490
pectin catabolic process
GO:0071555
cell wall organization
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0009279
cell outer membrane
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2ntb
,
PDBe:2ntb
,
PDBj:2ntb
PDBsum
2ntb
PubMed
17717531
UniProt
P0C1A9
|PMEA_DICD3 Pectinesterase A (Gene Name=pemA)
[
Back to BioLiP
]