Structure of PDB 1nvm Chain G Binding Site BS01
Receptor Information
>1nvm Chain G (length=339) Species:
79676
(Pseudomonas sp. CF600) [
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FNPSKKLYISDVTLRDGSHAIRHQYTLDDVRAIARALDKAKVDSIEVAHG
DGLQGSSFNYGFGRHTDLEYIEAVAGEISHAQIATLLLPGIGSVHDLKNA
YQAGARVVRVATHCTEADVSKQHIEYARNLGMDTVGFLMMSHMIPAEKLA
EQGKLMESYGATCIYMADSGGAMSMNDIRDRMRAFKAVLKPETQVGMHAH
HNLSLGVANSIVAVEEGCDRVDASLAGMGAGAGNAPLEVFIAVAERLGWN
HGTDLYTLMDAADDIVRPLQDRPVRVDRETLGLGYAGVYSSFLRHAEIAA
AKYNLKTLDILVELGHRRMVGGQEDMIVDVALDLLAAHK
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
1nvm Chain G Residue 3507 [
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Receptor-Ligand Complex Structure
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PDB
1nvm
Crystal structure of a bifunctional aldolase-dehydrogenase: Sequestering a reactive and volatile intermediate
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
D18 H200 H202
Binding residue
(residue number reindexed from 1)
D16 H198 H200
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D18 H21 H200 H202 Y291
Catalytic site (residue number reindexed from 1)
D16 H19 H198 H200 Y289
Enzyme Commision number
4.1.3.39
: 4-hydroxy-2-oxovalerate aldolase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003852
2-isopropylmalate synthase activity
GO:0005515
protein binding
GO:0008701
4-hydroxy-2-oxovalerate aldolase activity
GO:0016829
lyase activity
GO:0016833
oxo-acid-lyase activity
GO:0030145
manganese ion binding
GO:0046872
metal ion binding
Biological Process
GO:0009056
catabolic process
GO:0009098
L-leucine biosynthetic process
GO:0019336
phenol-containing compound catabolic process
GO:0043640
benzoate catabolic process via hydroxylation
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1nvm
,
PDBe:1nvm
,
PDBj:1nvm
PDBsum
1nvm
PubMed
12764229
UniProt
P51016
|HOA_PSEUF 4-hydroxy-2-oxovalerate aldolase (Gene Name=dmpG)
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