Structure of PDB 2rj4 Chain A Binding Site BS01
Receptor Information
>2rj4 Chain A (length=290) Species:
9606
(Homo sapiens) [
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FMVSLPRMVYPQPKVLTPCRKDVLVVTPWLAPIVWEGTFNIDILNEQFRL
QNTTIGLTVFAIKKYVAFLKLFLETAEKHFMVGHRVHYYVFTDQPAAVPR
VTLGTGRQLSVLEVRAYKRWQDVSMRRMEMISFCERRFLSEVDYLVCVDV
DMEFRDHVGVEILTPLFGTLHPSFYGSSREAFTYERRPQSQAYIPKDEGD
FYYMGAFFGGSVQEVQRLTRACHQAMMVDQANGIEAVWHDESHLNKYLLR
HKPTKVLSPEYLWDQQLLGWPAVLRKLRFTAVPKNHQAVR
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
2rj4 Chain A Residue 2 [
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Receptor-Ligand Complex Structure
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PDB
2rj4
ABO(H) blood group A and B glycosyltransferases recognize substrate via specific conformational changes.
Resolution
1.47 Å
Binding residue
(original residue number in PDB)
D211 D213
Binding residue
(residue number reindexed from 1)
D149 D151
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H233 M266 W300 E303 A343 R352
Catalytic site (residue number reindexed from 1)
H171 M204 W238 E241 A281 R290
Enzyme Commision number
2.4.1.37
: fucosylgalactoside 3-alpha-galactosyltransferase.
2.4.1.40
: glycoprotein-fucosylgalactoside alpha-N-acetylgalactosaminyltransferase.
Gene Ontology
Molecular Function
GO:0016758
hexosyltransferase activity
Biological Process
GO:0005975
carbohydrate metabolic process
Cellular Component
GO:0016020
membrane
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Cellular Component
External links
PDB
RCSB:2rj4
,
PDBe:2rj4
,
PDBj:2rj4
PDBsum
2rj4
PubMed
18192272
UniProt
P16442
|BGAT_HUMAN Histo-blood group ABO system transferase (Gene Name=ABO)
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