Structure of PDB 3gg2 Chain A Binding Site BS02
Receptor Information
>3gg2 Chain A (length=431) Species:
837
(Porphyromonas gingivalis) [
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SLDIAVVGIGYVGLVSATCFAELGANVRCIDTDRNKIEQLNSGTIPIYEP
GLEKMIARNVKAGRLRFGTEIEQAVPEADIIFIAVGTPAGEDGSADMSYV
LDAARSIGRAMSRYILIVTKSTVPVGSYRLIRKAIQEELDKREVLIDFDI
ASNPEFLKEGNAIDDFMKPDRVVVGVDSDRARELITSLYKPMLLNNFRVL
FMDIASAEMTKYAANAMLATRISFMNDVANLCERVGADVSMVRLGIGSDS
RIGSKFLYPGCGYGGSCFPKDVKALIRTAEDNGYRMEVLEAVERVNEKQK
SILFDKFSTYYKGNVQGRCVAIWGLSFKPGTDDMREAPSLVLIEKLLEVG
CRVRVYDPVAMKEAQKRLGDKVEYTTDMYDAVRGAEALFHVTEWKEFRMP
DWSALSQAMAASLVIDGRNVYELPFTLLNIG
Ligand information
Ligand ID
UGA
InChI
InChI=1S/C15H22N2O18P2/c18-5-1-2-17(15(26)16-5)12-9(22)6(19)4(32-12)3-31-36(27,28)35-37(29,30)34-14-10(23)7(20)8(21)11(33-14)13(24)25/h1-2,4,6-12,14,19-23H,3H2,(H,24,25)(H,27,28)(H,29,30)(H,16,18,26)/t4-,6-,7+,8+,9-,10-,11+,12-,14-/m1/s1
InChIKey
HDYANYHVCAPMJV-LXQIFKJMSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)C3OC(OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)NC(=O)C=C1)C(O)C2O)C(O)C(O)C3O
CACTVS 3.341
O[CH]1[CH](O)[CH](O[CH]([CH]1O)C(O)=O)O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)(O)O[P@@](=O)(O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)C(=O)O)O)O)O)O)O
CACTVS 3.341
O[C@@H]1[C@@H](O)[C@H](O[C@@H]([C@H]1O)C(O)=O)O[P@@](O)(=O)O[P@@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=CC(=O)NC3=O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)C(=O)O)O)O)O)O)O
Formula
C15 H22 N2 O18 P2
Name
URIDINE-5'-DIPHOSPHATE-GLUCURONIC ACID;
UDP-GLUCURONIC ACID
ChEMBL
CHEMBL228057
DrugBank
DB03041
ZINC
ZINC000008215691
PDB chain
3gg2 Chain A Residue 6000 [
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Receptor-Ligand Complex Structure
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PDB
3gg2
Crystal structure of UDP-glucose 6-dehydrogenase from Porphyromonas gingivalis bound to product UDP-glucuronate
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
M244 K245 L270 L271 N272 R275
Binding residue
(residue number reindexed from 1)
M167 K168 L193 L194 N195 R198
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
T199 E236 K288 N292 C344 D348
Catalytic site (residue number reindexed from 1)
T122 E159 K211 N215 C267 D271
Enzyme Commision number
1.1.1.22
: UDP-glucose 6-dehydrogenase.
Gene Ontology
Molecular Function
GO:0003979
UDP-glucose 6-dehydrogenase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0051287
NAD binding
Biological Process
GO:0000271
polysaccharide biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3gg2
,
PDBe:3gg2
,
PDBj:3gg2
PDBsum
3gg2
PubMed
UniProt
Q7MVC7
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