Structure of PDB 1xjg Chain A Binding Site BS02
Receptor Information
>1xjg Chain A (length=615) Species:
2336
(Thermotoga maritima) [
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MKLSDLISRWIDVEPSKNAQIILRDRYFMKDLDGNYLETKWEDVARRVAR
VVATAELLNPSYKKNEKLDRIKEWEDIFFRVLKARLFIPNSPTLFNAGLG
VKHDLLWKPIDQMTLEDYEEIYRSRNHLHMLSACFVVPVGDSIEEIFEAV
KEYALITKVGGGVGSNFSELRPKGSFVAGTHGKASGPVSFMHVFNSAISV
VKALMGILNINHPDIEEFIDAKKVLNFFNLSVGFPMDKKEILKLYEEDGE
LELSHPRSTIRKKVKIRELFRKIATNAWKSGDPGLAFLGEMNKYYPLYPH
RKINSTNPCGEIGLSDYEACNLGSIDVAKFYNNGFVDLEALQELVQIAVR
FLDNVIDVNVFPIDKITKAVKESRRLGLGIMGFADLLYKLEIPYNSQEAR
DFAANLMAFIALHAHRTSYELGKEKGNFPLLEISRYRTEDNFVPFAMGMS
NYDDEIREVMKMTKEFRRNVALLTIAPTGSISNIADTSSGLEPNFLLAYT
RFVTKEPLLYVNQVLREKLNPEILKRIEKELIEKGSLKDIPDVPEKIKKV
FVVALDIDPMDHLLMQDAFQRYVDNNISKTINMPQSATVDDVLNVYLEAL
RTNVRGITVYRDGSL
Ligand information
Ligand ID
DTP
InChI
InChI=1S/C10H16N5O12P3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(25-7)2-24-29(20,21)27-30(22,23)26-28(17,18)19/h3-7,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1
InChIKey
SUYVUBYJARFZHO-RRKCRQDMSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3C[C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3C[CH](O)[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)O3
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3CC(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@H]3C[C@H](O)[C@@H](CO[P@@](O)(=O)O[P@](O)(=O)O[P](O)(O)=O)O3
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)CC3O
Formula
C10 H16 N5 O12 P3
Name
2'-DEOXYADENOSINE 5'-TRIPHOSPHATE
ChEMBL
CHEMBL335538
DrugBank
DB03222
ZINC
ZINC000008215662
PDB chain
1xjg Chain A Residue 1004 [
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Receptor-Ligand Complex Structure
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PDB
1xjg
Structural Mechanism of Allosteric Substrate Specificity Regulation in a Ribonucleotide Reductase
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D141 S142 I143 R171 G179 T180 K183 S185
Binding residue
(residue number reindexed from 1)
D141 S142 I143 R171 G179 T180 K183 S185
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C134 N320 C322 E324 C333 T626 V627
Catalytic site (residue number reindexed from 1)
C134 N307 C309 E311 C320 T608 V609
Enzyme Commision number
1.17.4.1
: ribonucleoside-diphosphate reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004748
ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
GO:0005524
ATP binding
GO:0031419
cobalamin binding
Biological Process
GO:0009263
deoxyribonucleotide biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1xjg
,
PDBe:1xjg
,
PDBj:1xjg
PDBsum
1xjg
PubMed
15475969
UniProt
O33839
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