Structure of PDB 1gww Chain A Binding Site BS02
Receptor Information
>1gww Chain A (length=287) Species:
9913
(Bos taurus) [
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KLKLSDWFNPFKRPEVVTMTKWKAPVVWEGTYNRAVLDNYYAKQKITVGL
TVFAVGRYIEHYLEEFLTSANKHFMVGHPVIFYIMVDDVSRMPLIELGPL
RSFKVFKIKPEKRWQDISMMRMKTIGEHIVAHIQHEVDFLFCMDVDQVFQ
DKFGVETLGESVAQLQAWWYKADPNDFTYERRKESAAYIPFGEGDFYYHA
AIFGGTPTQVLNITQECFKGILKDKKNDIEAQWHDESHLNKYFLLNKPTK
ILSPEYCWDYHIGLPADIKLVKMSWQTKEYNVVRNNV
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
1gww Chain A Residue 1370 [
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Receptor-Ligand Complex Structure
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PDB
1gww
Structural Basis of Ordered Binding of Donor and Acceptor Substrates to the Retaining Glycosyltransferase, Alpha -1,3 Galactosyltransferase
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D225 D227
Binding residue
(residue number reindexed from 1)
D144 D146
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q247 H280 W314 E317 W356 R365
Catalytic site (residue number reindexed from 1)
Q166 H199 W233 E236 W275 R284
Enzyme Commision number
2.4.1.87
: N-acetyllactosaminide 3-alpha-galactosyltransferase.
Gene Ontology
Molecular Function
GO:0016758
hexosyltransferase activity
Biological Process
GO:0005975
carbohydrate metabolic process
Cellular Component
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1gww
,
PDBe:1gww
,
PDBj:1gww
PDBsum
1gww
PubMed
12011052
UniProt
P14769
|GGTA1_BOVIN N-acetyllactosaminide alpha-1,3-galactosyltransferase (Gene Name=GGTA1)
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