Structure of PDB 3gg2 Chain B Binding Site BS01
Receptor Information
>3gg2 Chain B (length=425) Species:
837
(Porphyromonas gingivalis) [
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LDIAVVGIGYVGLVSATCFAELGANVRCIDTDRNKIEQLNSGTIPIYEPG
LEKMIARNVKAGRLRFGTEIEQAVPEADIIFIAVGTPAGEDGSADMSYVL
DAARSIGRAMSRYILIVTKSTVPVGSYRLIRKAIQEELDKREVLIDFDIA
SNPEFLKEGNAIDDFMKPDRVVVGVDSDRARELITSLYKPMLRVLFMDIA
SAEMTKYAANAMLATRISFMNDVANLCERVGADVSMVRLGIGSDSRIGSK
FLYPGCGYGGSCFPKDVKALIRTAEDNGYRMEVLEAVERVNEKQKSILFD
KFSTYYKGNVQGRCVAIWGLSFKPGTDDMREAPSLVLIEKLLEVGCRVRV
YDPVAMKEAQKRLGDKVEYTTDMYDAVRGAEALFHVTEWKEFRMPDWSAL
SQAMAASLVIDGRNVYELFTLLNIG
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 B Residue 2000 [
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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)
Y88 E232 F233 L234 K235 K288 I299 F333 Y335 Y340 C344 F345 F404 K405
Binding residue
(residue number reindexed from 1)
Y10 E154 F155 L156 K157 K206 I217 F251 Y253 Y258 C262 F263 F322 K323
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)
T121 E158 K206 N210 C262 D266
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3gg2
,
PDBe:3gg2
,
PDBj:3gg2
PDBsum
3gg2
PubMed
UniProt
Q7MVC7
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