Structure of PDB 6kpr Chain B Binding Site BS01
Receptor Information
>6kpr Chain B (length=534) Species:
5833
(Plasmodium falciparum) [
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EQVCDVFDIYAICACCKVESEVFNNYTFRGLGNKGVLPWKCISLDMKYFR
AVTTYVNESKYEKLKYKRCKYLNKETVDSKKLQNVVVMGRTNWESIPKKF
KPLSNRINVILSRTLKKEDFDEDVYIINKVEDLIVLLGKLNYYKCFILGG
SVVYQEFLEKKLIKKIYFTRINSTYECDVFFPEINENEYQIISVSDVYTS
NNTTLDFIIYKKTNNDDEEEDDFVYFNFNKENKNSIHPNDFQIYNSLKYK
YHPEYQYLNIIYDIMMNGNKQSDRTGVGVLSKFGYIMKFDLSQYFPLLTT
KKLFLRGIIEELLWFIRGETNGNTLLNKNVRIWEANGTREFLDNRKLFHR
EVNDLGPIYGFQWRHFGAEYTNMYDNYENKGVDQLKNIINLIKNDPTSRR
ILLCAWNVKDLDQMALPPCHILCQFYVFDGKLSCIMYQRSCDLGLGVPFN
IASYSIFTHMIAQVCNLQPAQFIHVLGNAHVYNNHIDSLKIQLNRIPYPF
PTLKLNPDIKNIEDFTISDFTIQNYVHHEKISMD
Ligand information
Ligand ID
UMP
InChI
InChI=1S/C9H13N2O8P/c12-5-3-8(11-2-1-7(13)10-9(11)14)19-6(5)4-18-20(15,16)17/h1-2,5-6,8,12H,3-4H2,(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1
InChIKey
JSRLJPSBLDHEIO-SHYZEUOFSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=P(O)(O)OCC2OC(N1C(=O)NC(=O)C=C1)CC2O
CACTVS 3.370
O[CH]1C[CH](O[CH]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.7.6
C1[C@@H]([C@H](O[C@H]1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
CACTVS 3.370
O[C@H]1C[C@@H](O[C@@H]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.7.6
C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
Formula
C9 H13 N2 O8 P
Name
2'-DEOXYURIDINE 5'-MONOPHOSPHATE;
DUMP
ChEMBL
CHEMBL211312
DrugBank
DB03800
ZINC
ZINC000004228260
PDB chain
6kpr Chain A Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
6kpr
6-Hydrophobic aromatic substituent pyrimethamine analogues as potential antimalarials for pyrimethamine-resistant Plasmodium falciparum.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
R470 R471
Binding residue
(residue number reindexed from 1)
R399 R400
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
L46 D54 E382 W404 Y430 C490 R510 D513
Catalytic site (residue number reindexed from 1)
L37 D45 E311 W333 Y359 C419 R439 D442
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
2.1.1.45
: thymidylate synthase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004146
dihydrofolate reductase activity
GO:0004799
thymidylate synthase activity
GO:0008168
methyltransferase activity
GO:0016491
oxidoreductase activity
GO:0016741
transferase activity, transferring one-carbon groups
Biological Process
GO:0006231
dTMP biosynthetic process
GO:0006730
one-carbon metabolic process
GO:0009165
nucleotide biosynthetic process
GO:0032259
methylation
GO:0046654
tetrahydrofolate biosynthetic process
Cellular Component
GO:0005739
mitochondrion
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6kpr
,
PDBe:6kpr
,
PDBj:6kpr
PDBsum
6kpr
PubMed
31685330
UniProt
D9N170
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