Structure of PDB 3qke Chain D Binding Site BS01
Receptor Information
>3qke Chain D (length=396) Species:
158080
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LKIRDAYTIVTCPGRNFVTLKIVTESGTHGIGDATLNGREMAVAAYLDEH
VVPALIGRDAGRIEDTWQYLYRGAYWRRGPVTMTAIAAVDMALWDIKAKA
AGMPLYQLLGGKSRERVMTYAHCTGQTIEDCLGEVARHVELGYRAVRVQS
GVPGIETTYGVYEPADSSLPAEHVWSTEKYLNHAPKLFAAVRERFGDDLH
VLHDVHHRLTPIEAARLGKAVEPYHLFWLEDCVPAENQESLRLIREHTTT
PLAIGEVFNSIHDCRELIQNQWIDYIRMPLTHGGGITAMRRVADLASLYH
VRTGFHGPTDLSPVCLGAAIHFDTWVPNFGIQEHMPHTDETDAVFPHDYR
FEDGHFLAGESPGHGVDIDEELAAKYPYERASLPVNRLEDGTLWHW
Ligand information
Ligand ID
GCO
InChI
InChI=1S/C6H12O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-5,7-11H,1H2,(H,12,13)/t2-,3-,4+,5-/m1/s1
InChIKey
RGHNJXZEOKUKBD-SQOUGZDYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C([C@H]([C@H]([C@@H]([C@H](C(=O)O)O)O)O)O)O
OpenEye OEToolkits 1.5.0
C(C(C(C(C(C(=O)O)O)O)O)O)O
CACTVS 3.341
OC[CH](O)[CH](O)[CH](O)[CH](O)C(O)=O
CACTVS 3.341
OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O
ACDLabs 10.04
O=C(O)C(O)C(O)C(O)C(O)CO
Formula
C6 H12 O7
Name
D-gluconic acid;
GLUCONIC ACID
ChEMBL
CHEMBL464345
DrugBank
DB13180
ZINC
ZINC000001531008
PDB chain
3qke Chain D Residue 406 [
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Receptor-Ligand Complex Structure
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PDB
3qke
Cystal structure of D-mannonate dehydratase from Chromohalobacter salexigens complexed with Mg and D-Gluconate
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
N39 Y161 D213 H215 E265 H315 P317 D319 E342 W405
Binding residue
(residue number reindexed from 1)
N37 Y159 D204 H206 E256 H306 P308 D310 E333 W396
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H124 R149 Q151 Y161 D213 H215 E239 G264 E265 R286 P288 H315 G316 E342 W405
Catalytic site (residue number reindexed from 1)
H122 R147 Q149 Y159 D204 H206 E230 G255 E256 R277 P279 H306 G307 E333 W396
Enzyme Commision number
4.2.1.-
4.2.1.39
: gluconate dehydratase.
4.2.1.8
: mannonate dehydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0008927
mannonate dehydratase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
GO:0047929
gluconate dehydratase activity
Biological Process
GO:0009063
amino acid catabolic process
GO:0016052
carbohydrate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3qke
,
PDBe:3qke
,
PDBj:3qke
PDBsum
3qke
PubMed
UniProt
Q1QT89
|DMGD_CHRSD D-galactonate dehydratase family member ManD (Gene Name=manD)
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