Structure of PDB 6ckl Chain C Binding Site BS02
Receptor Information
>6ckl Chain C (length=225) Species:
487
(Neisseria meningitidis) [
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MEKQNIAVILARQNSKGLPLKNLRKMNGISLLGHTINAAISSKCFDRIIV
STDGGLIAEEAKNFGVEVVLRPAELASDTASSISGVIHALETIGSNSGTV
TLLQPTSPLRTGAHIREAFSLFDEKIKGSVVSACPMEHHPLKTLLQINNG
EYAPMRHLSDLEQPRQQLPQAFRPNGAIYINDTASLIANNCFFIAPTKLY
IMSHQDSIDIDTELDLQQAENILNH
Ligand information
Ligand ID
C5P
InChI
InChI=1S/C9H14N3O8P/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChIKey
IERHLVCPSMICTF-XVFCMESISA-N
SMILES
Software
SMILES
CACTVS 3.341
NC1=NC(=O)N(C=C1)[CH]2O[CH](CO[P](O)(O)=O)[CH](O)[CH]2O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)O)O)O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
ACDLabs 10.04
O=C1N=C(N)C=CN1C2OC(C(O)C2O)COP(=O)(O)O
Formula
C9 H14 N3 O8 P
Name
CYTIDINE-5'-MONOPHOSPHATE
ChEMBL
CHEMBL307679
DrugBank
DB03403
ZINC
ZINC000003861744
PDB chain
6ckl Chain C Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
6ckl
Catalytic Cycle ofNeisseria meningitidisCMP-Sialic Acid Synthetase Illustrated by High-Resolution Protein Crystallography.
Resolution
2.684 Å
Binding residue
(original residue number in PDB)
L10 A11 R12 N22 R71 Q104 T106
Binding residue
(residue number reindexed from 1)
L10 A11 R12 N22 R71 Q104 T106
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.7.7.43
: N-acylneuraminate cytidylyltransferase.
Gene Ontology
Molecular Function
GO:0008781
N-acylneuraminate cytidylyltransferase activity
GO:0016779
nucleotidyltransferase activity
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:6ckl
,
PDBe:6ckl
,
PDBj:6ckl
PDBsum
6ckl
PubMed
31583886
UniProt
P0A0Z8
|NEUA_NEIME N-acylneuraminate cytidylyltransferase (Gene Name=neuA)
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