Structure of PDB 2v2b Chain A Binding Site BS01
Receptor Information
>2v2b Chain A (length=272) Species:
562
(Escherichia coli) [
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QNITQSWFVQGMIKATTDAWLKGWDERNGGNLTLRLDDADIAPYHDNFHQ
QPRYIPLSQPMPLLANTPFIVTGSGKFFRNVQLDPAANLGIVKVDSDGAG
YHILWGLTNEAVPTSSLPAHFLSHCERIKATNGKDRVIMHCHATNLIALT
YVLENDTAVFTRQLWEGSTECLVVFPDGVGILPWMVPGTDAIGQATAQEM
QKHSLVLWPFHGVFGSGPTLDETFGLIDTAEKSAQVLVKVYSMGGMGQTI
SAAELIALGKRFGVTPLASALA
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2v2b Chain A Residue 1274 [
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Receptor-Ligand Complex Structure
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PDB
2v2b
Antenna Domain Mobility and Enzymatic Reaction of L-Rhamnulose-1-Phosphate Aldolase.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
H141 H143 H212
Binding residue
(residue number reindexed from 1)
H140 H142 H211
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S117 H141 H143 E171 H212
Catalytic site (residue number reindexed from 1)
S116 H140 H142 E170 H211
Enzyme Commision number
4.1.2.19
: rhamnulose-1-phosphate aldolase.
Gene Ontology
Molecular Function
GO:0008994
rhamnulose-1-phosphate aldolase activity
GO:0016829
lyase activity
GO:0016830
carbon-carbon lyase activity
GO:0016832
aldehyde-lyase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0005996
monosaccharide metabolic process
GO:0019299
rhamnose metabolic process
GO:0019301
rhamnose catabolic process
GO:0019323
pentose catabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2v2b
,
PDBe:2v2b
,
PDBj:2v2b
PDBsum
2v2b
PubMed
18085797
UniProt
P32169
|RHAD_ECOLI Rhamnulose-1-phosphate aldolase (Gene Name=rhaD)
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