Structure of PDB 5c49 Chain A Binding Site BS03
Receptor Information
>5c49 Chain A (length=277) Species:
9606
(Homo sapiens) [
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FMVSLPRMVYPQPKVLTPCRKDVLVVTPWLAPIVWEGTFNIDILNEQFRL
QNTTIGLTVFAIKKYVAFLKLFLETAEKHFMVGHRVHYYVFTDQPAAVPR
VTLGTGRQLSVLEVGVSMRRMEMISFCERRFLSEVDYLVCVDVDMEFRDH
VGVEILTPLFGTLHPSFYGSSREAFTYERRPQSQAYIPKDEGDFYYMGAF
FGGSVQEVQRLTRACHQAMMVDQANGIEAVWHDESHLNKYLLRHKPTKVL
SPEYLWDQQLLGWPAVLRKLRFTAVPK
Ligand information
Ligand ID
UDP
InChI
InChI=1S/C9H14N2O12P2/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(22-8)3-21-25(19,20)23-24(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChIKey
XCCTYIAWTASOJW-XVFCMESISA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)(O)OP(=O)(O)O)O)O
CACTVS 3.370
O[CH]1[CH](O)[CH](O[CH]1CO[P](O)(=O)O[P](O)(O)=O)N2C=CC(=O)NC2=O
CACTVS 3.370
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CO[P](O)(=O)O[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.7.0
C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)O)O)O
ACDLabs 12.01
O=P(O)(O)OP(=O)(O)OCC2OC(N1C(=O)NC(=O)C=C1)C(O)C2O
Formula
C9 H14 N2 O12 P2
Name
URIDINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL130266
DrugBank
DB03435
ZINC
ZINC000004490939
PDB chain
5c49 Chain A Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
5c49
High Resolution Structures of the Human ABO(H) Blood Group Enzymes in Complex with Donor Analogs Reveal That the Enzymes Utilize Multiple Donor Conformations to Bind Substrates in a Stepwise Manner.
Resolution
1.49 Å
Binding residue
(original residue number in PDB)
F121 A122 I123 Y126 R188 D211 V212 D213 K346
Binding residue
(residue number reindexed from 1)
F60 A61 I62 Y65 R120 D142 V143 D144 K277
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
H233 M266 W300 E303 A343
Catalytic site (residue number reindexed from 1)
H164 M197 W231 E234 A274
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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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5c49
,
PDBe:5c49
,
PDBj:5c49
PDBsum
5c49
PubMed
26374898
UniProt
P16442
|BGAT_HUMAN Histo-blood group ABO system transferase (Gene Name=ABO)
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