Structure of PDB 2hne Chain A Binding Site BS01
Receptor Information
>2hne Chain A (length=426) Species:
340
(Xanthomonas campestris pv. campestris) [
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MRTIIALETHDVRFPTSREPDPDYSAAYVVLRTDGAEDLAGYGLVFTIGR
GNDVQTAAVAALAEHVVGLSVDKVIADLGAFARRLTNDSQLRWLGPEKGV
MHMAIGAVINAAWDLAARAANKPLWRFIAELTPEQLVDTIDFRYLSDALT
RDEALAILRDAQPQRAARTATLIEQGYPAYTTSPGWLGYSDEKLVRLAKE
AVADGFRTIKLKVGANVQDDIRRCRLARAAIGPDIAMAVDANQRWDVGPA
IDWMRQLAEFDIAWIEEPTSPDDVLGHAAIRQGITPVPVSTGEHTQNRVV
FKQLLQAGAVDLIQIDAARVGGVNENLAILLLAAKFGVRVFPHAGGVGLC
ELVQHLAMADFVAITGKMEDRAIEFVDHLHQHFLDPVRIQHGRYLAPEVP
GFSAEMHPASIAEFSYPDGRFWVEDL
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
2hne Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
2hne
Crystal structure of l-fuconate dehydratase from xanthomonas campestris pv. campestris str. ATCC 33913
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D248 E274 E301
Binding residue
(residue number reindexed from 1)
D240 E266 E293
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T55 T190 K218 K220 D248 N250 E274 G300 E301 D324 P350 H351 A352 D368 K375 E382
Catalytic site (residue number reindexed from 1)
T47 T182 K210 K212 D240 N242 E266 G292 E293 D316 P342 H343 A344 D360 K367 E374
Enzyme Commision number
4.2.1.68
: L-fuconate dehydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0016829
lyase activity
GO:0016836
hydro-lyase activity
GO:0046872
metal ion binding
GO:0050023
L-fuconate dehydratase activity
Biological Process
GO:0016052
carbohydrate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2hne
,
PDBe:2hne
,
PDBj:2hne
PDBsum
2hne
PubMed
UniProt
Q8P3K2
|FUCD_XANCP L-fuconate dehydratase (Gene Name=XCC4069)
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