Structure of PDB 5noo Chain A

Receptor sequence
>5nooA (length=287) Species: 6239 (Caenorhabditis elegans) [Search protein sequence]
QVHLNQDEYKYLKQVEQILREGTRRDDRTGTGTISIFGMQSKYCLRNGTI
PLLTTKRVYWKGVLEELLWFISGSTDGKLLMEKNVKIWEKNGDRAFLDNL
GFTSREEGDLGPVYGFQWRHFGAKYVDCHTDYSGQGVDQLAEVIRQIKEQ
PDSRRIIMSAWNPSDLGQMVLPPCHTMCQFYVDNGELSCQLYQRSGDMGL
GVPFNLASYGLLTHMIAKVCGLKPGTLVHTLGDAHVYSNHVDALKIQLDR
EPYAFPKIRFTRDVASIDDFTSDMIALDDYKCHPKIP
3D structure
PDB5noo Crystal structures of nematode (parasitic T. spiralis and free living C. elegans), compared to mammalian, thymidylate synthases (TS). Molecular docking and molecular dynamics simulations in search for nematode-specific inhibitors of TS.
ChainA
Resolution2.9 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) E89 W111 Y137 C197 R217 D220
Catalytic site (residue number reindexed from 1) E66 W88 Y114 C174 R194 D197
Enzyme Commision number 2.1.1.45: thymidylate synthase.
Interaction with ligand
Site
#
Ligand Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01 UMP A C197 R217 S218 D220 G224 N228 H258 Y260 C174 R194 S195 D197 G201 N205 H235 Y237
BS02 D16 A Y82 I110 D220 L223 G224 F227 Y260 Y59 I87 D197 L200 G201 F204 Y237
Gene Ontology
Molecular Function
GO:0004799 thymidylate synthase activity
GO:0008168 methyltransferase activity
GO:0016741 transferase activity, transferring one-carbon groups
Biological Process
GO:0006231 dTMP biosynthetic process
GO:0006235 dTTP biosynthetic process
GO:0009165 nucleotide biosynthetic process
GO:0032259 methylation

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:5noo, PDBe:5noo, PDBj:5noo
PDBsum5noo
PubMed28826032
UniProtQ9Y052

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