Structure of PDB 8ukr Chain B Binding Site BS04
Receptor Information
>8ukr Chain B (length=1123) Species:
559292
(Saccharomyces cerevisiae S288C) [
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DESAPITAEDSWAVISAFFREKGLVSQQLDSFNQFVDYTLQDIICEDSTL
ILEQLARKYEISFGKIYVTKPMVNESDGVTHALYPQEARLRNLTYSSGLF
VDVKKRTYESGKVFIGRLPIMLRSKNCYLSEATESDLYKLKECPFDMGGY
FIINGSEKVLIAQERSAGNIVQVFKKAAPSPISHVAEIRSALEKGSRFIS
TLQVKLYGREGSSARTIKATLPYIKQDIPIVIIFRALGIIPDGEILEHIC
YDVNDWQMLEMLKPCVEDGFVIQDRETALDFIGRRKEKRIQYAKDILQKE
FLPHITQLEGFESRKAFFLGYMINRLLLCALDRKDQDDRDHFGKKRLDLA
GPLLAQLFKTLFKKLTKDIFRYMQRTVEELAINAKTITSGLKYALATGNW
GEQKKAMSSRAGVSQVLNRYTYSSTLSHLRRTNTPIAKPRQLHNTHWGLV
CPAETPEGQACGLVKNLSLMSCISVGTDPMPIITFLSEWGMEPLEDYVPH
QSPDATRVFVNGVWHGVHRNPARLMETLRTLRRKGDINPEVSMIRDIREK
ELKIFTDAGRVYRPLFIVEDDGHKELKVRKGHIAKLMATEYQDVEEYTWS
SLLNEGLVEYIDAEEEESILIAMQPEDLEPAELDVDPAKRIRVSHHATTF
THCEIHPSMILGVAASIIPFPDHNQSPRNTYQSAMGKQAMGVFLTNYNVR
MDTMANILYYPQKPLGTTRAMEYLKFRELPAGQNAIVAIACYSGYNQEDS
MIMNQSSIDRGLFRSLFFRSYMDQEKKYGMSITETFEKPQRTNTLRMKHG
TYDKLDDDGLIAPGVRVSGEDVIIGKTTPISAYHSKRDASTPLRSTENGI
VDQVLVTTNQDGLKFVKVRVRTTKIPQIGDKFASRHGQKGTIGITYRRED
MPFTAEGIVPDLIINPHAIPSRMTVAHLIECLLSKVAALSGNEGDASPFT
DITVEGISKLLREHGYQSRGFEVMYNGHTGKKLMAQIFFGPTYYQRLRHM
VDDKIHARARGPMQVLTRQPVEGRSRDGGLRFGEMERDCMIAHGAASFLK
ERLMEASDAFRVHICGICGLMTVIAKLNHNQFECKGCDNKIDIYQIHIPY
AAKLLFQELMAMNITPRLYTDRS
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
8ukr Chain B Residue 1302 [
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Receptor-Ligand Complex Structure
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PDB
8ukr
Molecular Mechanism of RNA Polymerase II Transcriptional Mutagenesis by the Epimerizable DNA Lesion, Fapy·dG.
Resolution
3.78 Å
Binding residue
(original residue number in PDB)
R766 D837 S1019 R1020
Binding residue
(residue number reindexed from 1)
R678 D749 S921 R922
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.7.6
: DNA-directed RNA polymerase.
Gene Ontology
Molecular Function
GO:0001055
RNA polymerase II activity
GO:0003677
DNA binding
GO:0003729
mRNA binding
GO:0003899
DNA-directed 5'-3' RNA polymerase activity
GO:0003968
RNA-dependent RNA polymerase activity
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0016779
nucleotidyltransferase activity
GO:0032549
ribonucleoside binding
GO:0034062
5'-3' RNA polymerase activity
GO:0046872
metal ion binding
Biological Process
GO:0001172
RNA-templated transcription
GO:0006351
DNA-templated transcription
GO:0006366
transcription by RNA polymerase II
GO:0006367
transcription initiation at RNA polymerase II promoter
GO:0006368
transcription elongation by RNA polymerase II
Cellular Component
GO:0000428
DNA-directed RNA polymerase complex
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005665
RNA polymerase II, core complex
GO:0005739
mitochondrion
GO:0010494
cytoplasmic stress granule
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8ukr
,
PDBe:8ukr
,
PDBj:8ukr
PDBsum
8ukr
PubMed
38393762
UniProt
P08518
|RPB2_YEAST DNA-directed RNA polymerase II subunit RPB2 (Gene Name=RPB2)
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