Structure of PDB 5uw0 Chain C Binding Site BS01
Receptor Information
>5uw0 Chain C (length=638) Species:
559292
(Saccharomyces cerevisiae S288C) [
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SRDLQNHLLFETATEVANRVGGIYSVLKSKAPITVAQYKDHYHLIGPLNK
ATYQNEVDILDWKKPEAFSDEMRPVQHALQTMESRGVHFVYGRWLIEGAP
KVILFDLDSVRGYSNEWKGDLWSLVGIPSPENDFETNDAILLGYTVAWFL
GEVAHLDSQHAIVAHFHQWLAGVALPLCRKRRIDVVTIFTTHATLLGRYL
CASGSFDFYNCLESVDVDHEAGRFGIYHRYCIERAAAHSADVFTTVSQIT
AFEAEHLLKRKPDGILPNGLNVIKFQAFHEFQNLHALKKEKINDFVRGHF
HGCFDFDLDNTLYFFIAGRYEYKNKGADMFIEALARLNYRLKVSGSKKTV
VAFIVMPAKNNSFTVEALKGQAEVRALENTVHEVTTSIGKRIFDHAIRYP
HNGLTTELPTDLGELLKSSDKVMLKRRILALRRPEGQLPPIVTHNMVDDA
NDLILNKIRQVQLFNSPSDRVKMIFHPEFLNANNPILGLDYDEFVRGCHL
GVFPSYYEPWGYTPAECTVMGVPSITTNVSGFGSYMEDLIETNQAKDYGI
YIVDRRFKAPDESVEQLVDYMEEFVKKTRRQRINQRNRTERLSDLLDWKR
MGLEYVKARQLALRRGYPDQFRELVGEELNDSNMDALA
Ligand information
Ligand ID
U2F
InChI
InChI=1S/C15H23FN2O16P2/c16-8-11(23)9(21)5(3-19)32-14(8)33-36(28,29)34-35(26,27)30-4-6-10(22)12(24)13(31-6)18-2-1-7(20)17-15(18)25/h1-2,5-6,8-14,19,21-24H,3-4H2,(H,26,27)(H,28,29)(H,17,20,25)/t5-,6-,8-,9-,10-,11-,12-,13-,14-/m1/s1
InChIKey
NGTCPFGWXMBZEP-NQQHDEILSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(OC1OC(C(O)C(O)C1F)CO)(O)OP(=O)(O)OCC3OC(N2C=CC(=O)NC2=O)C(O)C3O
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)CO)O)O)F)O)O
CACTVS 3.341
OC[C@H]1O[C@H](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)[C@H](F)[C@@H](O)[C@@H]1O
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)CO)O)O)F)O)O
CACTVS 3.341
OC[CH]1O[CH](O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O)[CH](F)[CH](O)[CH]1O
Formula
C15 H23 F N2 O16 P2
Name
URIDINE-5'-DIPHOSPHATE-2-DEOXY-2-FLUORO-ALPHA-D-GLUCOSE
ChEMBL
CHEMBL593830
DrugBank
DB03488
ZINC
ZINC000016051573
PDB chain
5uw0 Chain C Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
5uw0
Activated state yGsy2p in complex with UDP-2-fluoro-2-deoxy-glucose
Resolution
2.73 Å
Binding residue
(original residue number in PDB)
R20 G23 I24 S26 H193 R199 R320 K326 F480 Y492 E509 W511 G512 Y513 T514 E517
Binding residue
(residue number reindexed from 1)
R19 G22 I23 S25 H192 R198 R319 K325 F479 Y491 E508 W510 G511 Y512 T513 E516
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.4.1.11
: glycogen(starch) synthase.
Gene Ontology
Molecular Function
GO:0004373
alpha-1,4-glucan glucosyltransferase (UDP-glucose donor) activity
GO:0005515
protein binding
GO:0016757
glycosyltransferase activity
GO:0042802
identical protein binding
GO:2001069
glycogen binding
Biological Process
GO:0005978
glycogen biosynthetic process
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0042587
glycogen granule
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5uw0
,
PDBe:5uw0
,
PDBj:5uw0
PDBsum
5uw0
PubMed
UniProt
P27472
|GYS2_YEAST Glycogen [starch] synthase isoform 2 (Gene Name=GSY2)
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