Structure of PDB 2apc Chain A Binding Site BS05
Receptor Information
>2apc Chain A (length=342) Species:
9986
(Oryctolagus cuniculus) [
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AVIPILVIACDRSTVRRCLDKLLHYRPSAELFPIIVSQDCGHEETAQVIA
SYGSAVTHIRQPDLSNIAVQPDHRKFQGYYKIARHYRWALGQIFHNFNYP
AAVVVEDDLEVAPDFFEYFQATYPLLKADPSLWCVSAWNDNGKEQMVDSS
KPELLYRTDFFPGLGWLLLAELWAELEPKWPKAFWDDWMRRPEQRKGRAC
VRPEISRTMTFGRKGVSHGQFFDQHLKFIKLNQQFVPFTQLDLSYLQQEA
YDRDFLARVYGAPQLQVEKVRTNDRKELGEVRVQYTGRDSFKAFAKALGV
MDDLKSGVPRAGYRGIVTFLFRGRRVHLAPPQTWDGYDPSWT
Ligand information
Ligand ID
GOL
InChI
InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
InChIKey
PEDCQBHIVMGVHV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(C(CO)O)O
ACDLabs 12.01
CACTVS 3.370
OCC(O)CO
Formula
C3 H8 O3
Name
GLYCEROL;
GLYCERIN;
PROPANE-1,2,3-TRIOL
ChEMBL
CHEMBL692
DrugBank
DB09462
ZINC
ZINC000000895048
PDB chain
2apc Chain A Residue 455 [
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Receptor-Ligand Complex Structure
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PDB
2apc
X-ray Crystal Structures of Rabbit N-acetylglucosaminyltransferase I (GnT I) in Complex with Donor Substrate Analogues.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
P235 R303
Binding residue
(residue number reindexed from 1)
P130 R198
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D213 D291
Catalytic site (residue number reindexed from 1)
D108 D186
Enzyme Commision number
2.4.1.101
: alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase.
Gene Ontology
Molecular Function
GO:0008375
acetylglucosaminyltransferase activity
Biological Process
GO:0006486
protein glycosylation
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Molecular Function
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Biological Process
External links
PDB
RCSB:2apc
,
PDBe:2apc
,
PDBj:2apc
PDBsum
2apc
PubMed
16769084
UniProt
P27115
|MGAT1_RABIT Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase (Gene Name=MGAT1)
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