Structure of PDB 4coj Chain A Binding Site BS05
Receptor Information
>4coj Chain A (length=594) Species:
243274
(Thermotoga maritima MSB8) [
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MKVQYSFEREFEELMSDLLSKYGYEMFQMDGLGDQLDVVKFTEDFVRTNI
STYFIEISKPHTYLYSLYRIWQKMKEMFGKGVADEFVEAQINGAVYLHDR
HHAALMPYCFAYTLKPIVEKGLPFIKTIKSEPAKHLSTFIQHVIQFVMFA
SNQSSGAVGLPDFFVWMWYFVKKDLKEGIIPRDKLDWYIEQHFQILTYSL
NQPIRTTQSPYTNFTYLDRNYIKAIFEGERYPDGSLITDHVEDIIALQKH
YWEWVSRERERQMFTFPVLTASLLYKDGKFLDEDSARFINKINMKWQDTN
WYISDSIDAVASCCEKLKGRMNSIGGSDLNIGSFKVITVNLPRIALESGG
DREKYLQILRHRVQLIKKALAAVREIIKERISEGLLPLYENGLMLLNRQY
GTIGVTGVWESASIMGLTTEDIDGLKYTEEGEVFVDNVLDTIREEAEKGY
HEYGFTFNIEQVPAEKAAVTLAQKDRFLFGEKQPFEIYSNQWVPLMANTD
VLNRIRYSGKWDKKVSGGAILHINLKTEEESFNMVKMIADMGVMYFAFNT
KISVCEDGHAFYGERCPVCGKAKVDEYMRIVGYLVPVSAFNKER
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
4coj Chain B Residue 654 [
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Receptor-Ligand Complex Structure
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PDB
4coj
The Crystal Structure of Thermotoga Maritima Class III Ribonucleotide Reductase Lacks a Radical Cysteine Pre-Positioned in the Active Site.
Resolution
2.48 Å
Binding residue
(original residue number in PDB)
S146 E147 K150 H151 T154 Q157 H158 Q161
Binding residue
(residue number reindexed from 1)
S130 E131 K134 H135 T138 Q141 H142 Q145
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.17.4.2
: ribonucleoside-triphosphate reductase (thioredoxin).
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004748
ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
GO:0008998
ribonucleoside-triphosphate reductase (thioredoxin) activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
Biological Process
GO:0006260
DNA replication
GO:0009265
2'-deoxyribonucleotide biosynthetic process
Cellular Component
GO:0031250
anaerobic ribonucleoside-triphosphate reductase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4coj
,
PDBe:4coj
,
PDBj:4coj
PDBsum
4coj
PubMed
26147435
UniProt
Q9WYL6
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