Structure of PDB 1h78 Chain A Binding Site BS02
Receptor Information
>1h78 Chain A (length=534) Species:
10665
(Tequatrovirus T4) [
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DSRVFPTQRDLMAGIVSKHIAKNMVPSFIMKAHESGIIHVHDIDYSPALP
FTNCCLVDLKGMLENGFKLGNAQIETPKSIGVATAIMAQITAQVASHQYG
GTTFANVDKVLSPYVKRTYAKHIEDAEKWQIADALNYAQSKTEKDVYDAF
QAYEYEVNTLFSSNTPFVTITFGTGTDWTERMIQKAILKNRIKGLGRDGI
TPIFPKLVMFVEEGVNLYKDDPNYDIKQLALECASKRMYPDIISAKNNKA
ITGSSVPVSPMGCRSFLSVWKDSTGNEILDGRNNLGVVTLNLPRIALDSY
IGTQFNEQKFVELFNERMDLCFEALMCRISSLKGVKATVAPILYQEGAFG
VRLKPDDDIIELFKNGRSSVSLGYIGIHELNILVGRDIGREILTKMNAHL
KQWTERTGFAFSLYSTPAENLCYRFCKLDTEKYGSVKDVTDKGWYTNSFH
VSVEENITPFEKISREAPYHFIATGGHISYVELPDMKNNLKGLEAVWDYA
AQHLDYFGVNMPVDKCFTMNTIRRTCAYLGNPNE
Ligand information
Ligand ID
DCP
InChI
InChI=1S/C9H16N3O13P3/c10-7-1-2-12(9(14)11-7)8-3-5(13)6(23-8)4-22-27(18,19)25-28(20,21)24-26(15,16)17/h1-2,5-6,8,13H,3-4H2,(H,18,19)(H,20,21)(H2,10,11,14)(H2,15,16,17)/t5-,6+,8+/m0/s1
InChIKey
RGWHQCVHVJXOKC-SHYZEUOFSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)N=C(N)C=C1)CC2O
OpenEye OEToolkits 1.5.0
C1C(C(OC1N2C=CC(=NC2=O)N)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[C@H]2C[C@H](O)[C@@H](CO[P@](O)(=O)O[P@](O)(=O)O[P](O)(O)=O)O2
OpenEye OEToolkits 1.5.0
C1[C@@H]([C@H](O[C@H]1N2C=CC(=NC2=O)N)CO[P@@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[CH]2C[CH](O)[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)O2
Formula
C9 H16 N3 O13 P3
Name
2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL560403
DrugBank
DB03258
ZINC
ZINC000008215945
PDB chain
1h78 Chain A Residue 1589 [
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Receptor-Ligand Complex Structure
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PDB
1h78
Structural Basis for Allosteric Substrate Specificty Regulation in Anaerobic Ribonucleotide Reductase
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
I99 E100 K103 V107 I111 Q114 K146
Binding residue
(residue number reindexed from 1)
I74 E75 K78 V82 I86 Q89 K121
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N78 C79 M288 C290 S292 N311 Y441 E446 A580
Catalytic site (residue number reindexed from 1)
N53 C54 M261 C263 S265 N284 Y414 E419 A527
Enzyme Commision number
1.1.98.6
: ribonucleoside-triphosphate reductase (formate).
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
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:1h78
,
PDBe:1h78
,
PDBj:1h78
PDBsum
1h78
PubMed
11587648
UniProt
P07071
|NRDD_BPT4 Anaerobic ribonucleoside-triphosphate reductase (Gene Name=nrdD)
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