Structure of PDB 4x3v Chain B Binding Site BS02
Receptor Information
>4x3v Chain B (length=738) Species:
9606
(Homo sapiens) [
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MHVIKRDGRQERVMFDKITSRIQKLCYGLNMDFVDPAQITMKVIQGLYSG
VTTVELDTLAAETAATLTTKHPDYAILAARIAVSNLHKETKKVFSDVMED
LYNYINPHNGKHSPMVAKSTLDIVLANKDRLNSAIIYDRDFSYNYFGFKT
LERSYLLKINGKVAERPQHMLMRVSVGIHKEDIDAAIETYNLLSERWFTH
ASPTLFNAGTNRPQLSSCFLLSMKDDSIEGIYDTLKQCALISKSAGGIGV
AVSCIRATGSYIAGTNGNSNGLVPMLRVYNNTARYVDQGGNPGAFAIYLE
PWHLDIFEFLDLKKNTGKEEQRARDLFFALWIPDLFMKRVETNQDWSLMC
PNECPGLDEVWGEEFEKLYASYEKQGRVRKVVKAQQLWYAIIESQTETGT
PYMLYKDSCNRKSNQQNLGTIKCSNLCTEIVEYTSKDEVAVCNLASLALN
MYVTSEHTYDFKKLAEVTKVVVRNLNKIIDINYYPVPEACLSNKRHRPIG
IGVQGLADAFILMRYPFESAEAQLLNKQIFETIYYGALEASCDLAKEQGP
YETYEGSPVSKGILQYDMWNVTPTDLWDWKVLKEKIAKYGIRNSLLIAPM
PTASTAQILGNNESIEPYTSNIYTRRVGEFQIVNPHLLKDLTERGLWHEE
MKNQIIACNGSIQSIPEIPDDLKQLYKTVWEISQKTVLKMAAERGAFIDQ
SQSLNIHIAEPNYGKLTSMHFYGWKQGLKTGMYYLRTR
Ligand information
Ligand ID
TTP
InChI
InChI=1S/C10H17N2O14P3/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(24-8)4-23-28(19,20)26-29(21,22)25-27(16,17)18/h3,6-8,13H,2,4H2,1H3,(H,19,20)(H,21,22)(H,11,14,15)(H2,16,17,18)/t6-,7+,8+/m0/s1
InChIKey
NHVNXKFIZYSCEB-XLPZGREQSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)CO[P@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O
CACTVS 3.341
CC1=CN([CH]2C[CH](O)[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)O2)C(=O)NC1=O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)NC(=O)C(=C1)C)CC2O
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O
CACTVS 3.341
CC1=CN([C@H]2C[C@H](O)[C@@H](CO[P@@](O)(=O)O[P@](O)(=O)O[P](O)(O)=O)O2)C(=O)NC1=O
Formula
C10 H17 N2 O14 P3
Name
THYMIDINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL363559
DrugBank
DB02452
ZINC
ZINC000008215959
PDB chain
4x3v Chain B Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
4x3v
Identification of Non-nucleoside Human Ribonucleotide Reductase Modulators.
Resolution
3.7 Å
Binding residue
(original residue number in PDB)
D226 S227 I228 R256 I262 A263 G264 S269
Binding residue
(residue number reindexed from 1)
D226 S227 I228 R256 I262 A263 G264 S269
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C218 N427 C429 E431 C444 Y737 Y738
Catalytic site (residue number reindexed from 1)
C218 N425 C427 E429 C442 Y733 Y734
Enzyme Commision number
1.17.4.1
: ribonucleoside-diphosphate reductase.
Gene Ontology
Molecular Function
GO:0004748
ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016491
oxidoreductase activity
GO:0017076
purine nucleotide binding
GO:0042802
identical protein binding
GO:0061731
ribonucleoside-diphosphate reductase activity
GO:0097718
disordered domain specific binding
Biological Process
GO:0000731
DNA synthesis involved in DNA repair
GO:0006206
pyrimidine nucleobase metabolic process
GO:0006264
mitochondrial DNA replication
GO:0006281
DNA repair
GO:0008584
male gonad development
GO:0009185
ribonucleoside diphosphate metabolic process
GO:0009263
deoxyribonucleotide biosynthetic process
GO:0009265
2'-deoxyribonucleotide biosynthetic process
GO:0010212
response to ionizing radiation
GO:0010971
positive regulation of G2/M transition of mitotic cell cycle
GO:0021846
cell proliferation in forebrain
GO:0051290
protein heterotetramerization
GO:0060041
retina development in camera-type eye
GO:0070318
positive regulation of G0 to G1 transition
GO:1900087
positive regulation of G1/S transition of mitotic cell cycle
Cellular Component
GO:0005635
nuclear envelope
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0005971
ribonucleoside-diphosphate reductase complex
GO:0042995
cell projection
GO:0043025
neuronal cell body
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4x3v
,
PDBe:4x3v
,
PDBj:4x3v
PDBsum
4x3v
PubMed
26488902
UniProt
P23921
|RIR1_HUMAN Ribonucleoside-diphosphate reductase large subunit (Gene Name=RRM1)
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