Structure of PDB 1xpg Chain A Binding Site BS02
Receptor Information
>1xpg Chain A (length=734) Species:
2336
(Thermotoga maritima) [
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FTKAYAFGFPKIGEKREFKKALEDFWKGKITEEQFEEEMNKLRMYMVENY
RKNVDVIPSNELSYYDFVLDTAVMVGAVPERFGEYRGLSTYFDMARGGKA
LEMTKFFNTNYHYLVPEIETEEFYLLENKPLEDYLFFKSKGIETAPWVIG
PFTFLYLSKRNGEWIRRPNQMEKLLESLVSVYKEVFEKLVENGCKEILVN
EPAFVCDLEKAHWDLILNVYRELSEFPLTVFTYYDSVSDYEACVSLPVKR
LHFDFVSNEENLKNLEKHGFPEDKKLVAGVINGRQPWKVDLRKVASLVEK
LGASAISNSCPLFHLPVTLELENNLPGGLKEKLAFAKEKLEELKMLKDFL
EGKTFDLPNVSFEDFAVDLQAVERVRNLPEDSFRREKEYTERDRIQRERL
NLPLFPTTTIGSFPQTPEVRKMRSKYRKGEISKEEYEAFIKEQIKKAIEL
QEEIGLDVLVHGEFERTDMVEFFAEKLNGIATTQNGWVLSYGSRCYRPPI
IYGTVTRPEPMTLKEITYAQSLTEKPVKGMLTGPVTIMSWSYYREDIPER
EIAYQIALAINEEVKDLEEAGIKIVQIDEPAFREKAPIKKSKWPEYFEWA
INAFNLAANARPETQIHAHMCYSDFNEIIEYIHQLEFDVISIEASRSKGE
IISAFENFKGWIKQIGVGVWDIHSPAVPSINEMREIVERVLRVLPKELIW
INPDCGLKTRNWDEVIPSLRNMVALAKEMREKFA
Ligand information
Ligand ID
C2F
InChI
InChI=1S/C20H25N7O6/c1-27-12(9-23-16-15(27)18(31)26-20(21)25-16)8-22-11-4-2-10(3-5-11)17(30)24-13(19(32)33)6-7-14(28)29/h2-5,12-13,22H,6-9H2,1H3,(H,24,30)(H,28,29)(H,32,33)(H4,21,23,25,26,31)/t12-,13-/m0/s1
InChIKey
ZNOVTXRBGFNYRX-STQMWFEESA-N
SMILES
Software
SMILES
CACTVS 3.341
CN1[CH](CNc2ccc(cc2)C(=O)N[CH](CCC(O)=O)C(O)=O)CNC3=C1C(=O)NC(=N3)N
ACDLabs 10.04
O=C(O)C(NC(=O)c1ccc(cc1)NCC2N(C=3C(=O)NC(=NC=3NC2)N)C)CCC(=O)O
OpenEye OEToolkits 1.5.0
CN1C(CNC2=C1C(=O)NC(=N2)N)CNc3ccc(cc3)C(=O)NC(CCC(=O)O)C(=O)O
OpenEye OEToolkits 1.5.0
C[N@@]1[C@H](CNC2=C1C(=O)NC(=N2)N)CNc3ccc(cc3)C(=O)N[C@@H](CCC(=O)O)C(=O)O
CACTVS 3.341
CN1[C@@H](CNc2ccc(cc2)C(=O)N[C@@H](CCC(O)=O)C(O)=O)CNC3=C1C(=O)NC(=N3)N
Formula
C20 H25 N7 O6
Name
5-METHYL-5,6,7,8-TETRAHYDROFOLIC ACID
ChEMBL
CHEMBL1231574
DrugBank
DB11256
ZINC
ZINC000002005305
PDB chain
1xpg Chain A Residue 1882 [
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Receptor-Ligand Complex Structure
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PDB
1xpg
Cobalamin-independent methionine synthase (MetE): a face-to-face double barrel that evolved by gene duplication
Resolution
2.59 Å
Binding residue
(original residue number in PDB)
K18 K104 S489 R493 C494 W539 E583
Binding residue
(residue number reindexed from 1)
K19 K105 S490 R494 C495 W540 E584
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.1.1.14
: 5-methyltetrahydropteroyltriglutamate--homocysteine S-methyltransferase.
Gene Ontology
Molecular Function
GO:0003871
5-methyltetrahydropteroyltriglutamate-homocysteine S-methyltransferase activity
GO:0008168
methyltransferase activity
GO:0008270
zinc ion binding
GO:0046872
metal ion binding
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009086
methionine biosynthetic process
GO:0032259
methylation
GO:0071266
'de novo' L-methionine biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1xpg
,
PDBe:1xpg
,
PDBj:1xpg
PDBsum
1xpg
PubMed
15630480
UniProt
Q9X112
|METE_THEMA 5-methyltetrahydropteroyltriglutamate--homocysteine methyltransferase (Gene Name=metE)
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