Structure of PDB 1xjn Chain B Binding Site BS01
Receptor Information
>1xjn Chain B (length=610) Species:
2336
(Thermotoga maritima) [
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MKLSDLISRWIDVEPSKNAQIILRDRYFMKDLDGNYLETKWEDVARRVAR
VVATAELLNPSYKKNEKLDRIKEWEDIFFRVLKARLFIPNSPTLFNAGLG
VKHDLLWKPIDQMTLEDYEEIYRSRNHLHMLSACFVVPVGDSIEEIFEAV
KEYALITKVGGGVGSNFSELRPKGSFVAGTHGKASGPVSFMHVFNSAISV
VKQRRGALMGILNINHPDIEEFIDAKKVLNFFNLSVGFPMDKKEILKLYE
EDGELELSHPRSTIRKKVKIRELFRKIATNAWKSGDPGLAFLGEMNKYYP
LYPHRKINSTNPCGEIGLSDYEACNLGSIDVAKFYNNGFVDLEALQELVQ
IAVRFLDNVIDVNVFPIDKITKAVKESRRLGLGIMGFADLLYKLEIPYNS
QEARDFAANLMAFIALHAHRTSYELGKEKGNFPLLEISRYRTEDNFVPFA
MGMSNYDDEIREVMKMTKEFRRNVALLTIAPTGSISNIADTSSGLEPNFL
LAYTRPLLYVNQVLREKLNPEIEKELIEKGSLKDIPDVPEKIKKVFVVAL
DIDPMDHLLMQDAFQRYVDNNISKTINMPQSATVDDVLNVYLEALRTNVR
GITVYRDGSL
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
1xjn Chain A Residue 1005 [
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Receptor-Ligand Complex Structure
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PDB
1xjn
Structural Mechanism of Allosteric Substrate Specificity Regulation in a Ribonucleotide Reductase
Resolution
2.25 Å
Binding residue
(original residue number in PDB)
K158 V201 K202
Binding residue
(residue number reindexed from 1)
K158 V201 K202
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 N311 C313 E315 C324 T603 V604
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:1xjn
,
PDBe:1xjn
,
PDBj:1xjn
PDBsum
1xjn
PubMed
15475969
UniProt
O33839
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