Structure of PDB 6ckl Chain B Binding Site BS03
Receptor Information
>6ckl Chain B (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 B Residue 303 [
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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 A80 Q104 T106
Binding residue
(residue number reindexed from 1)
L10 A11 R12 N22 R71 A80 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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