Structure of PDB 6pd2 Chain A Binding Site BS04
Receptor Information
>6pd2 Chain A (length=615) Species:
243275
(Treponema denticola ATCC 35405) [
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MIKQAVILAGGLGSRLKDKTKTMPKGFLEIGGTAIVEQSVQKLLAHGIEK
IVIGTGHCNEYYDNLAKKYPAIITVKNENYANTGSMGTLEVCASFVNESF
LLLESDLIYDSAGLFSLINDERKNLILASGATKSGDEVYLEADEKNCLTG
LSKNRDALKNIFGELVGITKLTKSTLDKMCAYAKIHHSDLPKMEYEHALL
EAAKTIPVAIKRIEYFVWREIDNEDHLEMAVKNIYPHIVENEKLRAVRRE
VLLNPGPATTTDSVKYAQVSADICPREKAFGDLMQWLCDELKLFALASET
NPDEYETVMFGCSGTGADEVMVSSCVPDTGRLLVIDNGSYGARMAKIADI
YKIPMDIFKSSTYEPLDLQKLEAEFATKKYTHLACVYHETTTGLLNPLHI
ICPMAKKYGMVTIVDAVSAYCGMPMDLKSLGIDFMASTSNKNIQGMAGVG
FVICNKAELEKTKDYPMRNYYLNLYDQYAYFAKTHQTRFTPPVQTMYALR
QAVLETKQETVQKRYERYTACWNILVAAIKKLGLKMLVKEEHQSHFITAI
LEPETPKYSFEALHDFAAEHSFTIYPGKLGNIDTFRIANIGDIQPEEMRR
FTVKLKEYMNGIGVG
Ligand information
Ligand ID
0RC
InChI
InChI=1S/C11H20N4O10P2/c12-2-4-26(19,20)25-27(21,22)23-5-6-8(16)9(17)10(24-6)15-3-1-7(13)14-11(15)18/h1,3,6,8-10,16-17H,2,4-5,12H2,(H,19,20)(H,21,22)(H2,13,14,18)/t6-,8-,9-,10-/m1/s1
InChIKey
FBADRUOBFLBKJQ-PEBGCTIMSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@](=O)(O)O[P@@](=O)(CCN)O)O)O
CACTVS 3.341
NCC[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O)N2C=CC(=NC2=O)N
CACTVS 3.341
NCC[P@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=CC(=NC2=O)N
ACDLabs 10.04
O=P(O)(OP(=O)(O)OCC2OC(N1C(=O)N=C(N)C=C1)C(O)C2O)CCN
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=O)(CCN)O)O)O
Formula
C11 H20 N4 O10 P2
Name
5'-O-[(S)-{[(R)-(2-aminoethyl)(hydroxy)phosphoryl]oxy}(hydroxy)phosphoryl]cytidine
ChEMBL
DrugBank
ZINC
ZINC000008220008
PDB chain
6pd2 Chain A Residue 705 [
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Receptor-Ligand Complex Structure
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PDB
6pd2
The predominance of nucleotidyl activation in bacterial phosphonate biosynthesis.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
L8 A9 G10 G11 K25 T83 G84 S85 T88 E104 S105 D106 D136 E196 E220 D222
Binding residue
(residue number reindexed from 1)
L8 A9 G10 G11 K25 T83 G84 S85 T88 E104 S105 D106 D136 E196 E220 D222
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.6.1.37
: 2-aminoethylphosphonate--pyruvate transaminase.
2.7.7.107
: (2-aminoethyl)phosphonate cytidylyltransferase.
Gene Ontology
Molecular Function
GO:0008483
transaminase activity
GO:0016779
nucleotidyltransferase activity
GO:0046872
metal ion binding
GO:0047304
2-aminoethylphosphonate-pyruvate transaminase activity
Biological Process
GO:0019700
organic phosphonate catabolic process
GO:0032923
organic phosphonate biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6pd2
,
PDBe:6pd2
,
PDBj:6pd2
PDBsum
6pd2
PubMed
31420548
UniProt
Q73MU2
|PNTCW_TREDE Bifunctional 2-aminoethylphosphonate cytidylyltransferase/aminotransferase (Gene Name=pntC)
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