Structure of PDB 4d11 Chain A Binding Site BS04
Receptor Information
>4d11 Chain A (length=491) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
KVRWPDFNQEAYVGGTMVRSGQDPYARNKFNQVESDKLRMDRAIPDTRHD
QCQRKQWRVDLPATSVVITFHNEARSALLRTVVSVLKKSPPHLIKEIILV
DDYSNDPEDGALLGKIEKVRVLRNDRREGLMRSRVRGADAAQAKVLTFLD
SHCECNEHWLEPLLERVAEDRTRVVSPIIDVINMDNFQYVGASADLKGGF
DWNLVFKWDYMTPEQRRSRQGNPVAPIKTPMIAGGLFVMDKFYFEELGKY
DMMMDVWGGENLEISFRVWQCGGSLEIIPCSRVGHVFRKQHPYGSGTVFA
RNTRRAAEVWMDEYKNFYYAAVPSARNVPYGNIQSRLELRKKLSCKPFKW
YLENVYPELRVPDHQDIAFGALQQGTNCLDTLGHFADGVVGVYECHNAGG
NQEWALTKEKSVKHMDLCLTVVDRAPGSLIKLQGCREDDSRQKWEQIEGN
SKLRHVGSNLCLDSRTAKSGGLSVEVCGPALSQQWKFTLNL
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
4d11 Chain A Residue 1572 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
4d11
Substrate-Guided Front-Face Reaction Revealed by Combined Structural Snapshots and Metadynamics for the Polypeptide N- Acetylgalactosaminyltransferase 2.
Resolution
2.85 Å
Binding residue
(original residue number in PDB)
T143 D176 R201 G203 L204 D224 S225 H226 W331 H359 Y367
Binding residue
(residue number reindexed from 1)
T69 D102 R127 G129 L130 D150 S151 H152 W257 H285 Y293
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.4.1.41
: polypeptide N-acetylgalactosaminyltransferase.
Gene Ontology
Molecular Function
GO:0004653
polypeptide N-acetylgalactosaminyltransferase activity
GO:0005515
protein binding
GO:0016757
glycosyltransferase activity
GO:0030145
manganese ion binding
GO:0030246
carbohydrate binding
GO:0046872
metal ion binding
Biological Process
GO:0006486
protein glycosylation
GO:0006493
protein O-linked glycosylation
GO:0016266
O-glycan processing
GO:0018242
protein O-linked glycosylation via serine
GO:0018243
protein O-linked glycosylation via threonine
GO:0051604
protein maturation
Cellular Component
GO:0000139
Golgi membrane
GO:0005576
extracellular region
GO:0005789
endoplasmic reticulum membrane
GO:0005794
Golgi apparatus
GO:0005795
Golgi stack
GO:0016020
membrane
GO:0032580
Golgi cisterna membrane
GO:0048471
perinuclear region of cytoplasm
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4d11
,
PDBe:4d11
,
PDBj:4d11
PDBsum
4d11
PubMed
24954443
UniProt
Q10471
|GALT2_HUMAN Polypeptide N-acetylgalactosaminyltransferase 2 (Gene Name=GALNT2)
[
Back to BioLiP
]