Structure of PDB 1fa0 Chain B Binding Site BS03
Receptor Information
>1fa0 Chain B (length=511) Species:
4932
(Saccharomyces cerevisiae) [
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SSQKVFGITGPVSTVGATAAENKLNDSLIQELKKEGSFETEQETANRVQV
LKILQELAQRFVYEVSKKKNMSDGMARDAGGKIFTYGSYRLGVHGPGSDI
DTLVVVPKHVTREDFFTVFDSLLRERKELDEIAPVPDAFVPIIKIKFSGI
SIDLICARLDQPQVPLSLTLSDKNLLRNLDEKDLRALNGTRVTDEILELV
PKPNVFRIALRAIKLWAQRRAVYANIFGFPGGVAWAMLVARICQLYPNAC
SAVILNRFFIILSEWNWPQPVILKPIEDGPLQVRVWNPKIYAQDRSHRMP
VITPAYPSMCATHNITESTKKVILQEFVRGVQITNDIFSNKKSWANLFEK
NDFFFRYKFYLEITAYTRGSDEQHLKWSGLVESKVRLLVMKLEVLAGIKI
AHPFTKPFESSYCCPTEDDYEMIQDKYGSHKTETALNALKLVTPKAYLST
MYIGLDFNIVDIHIPCTEFVNLCRSFNEDYGDHKVFNLALRFVKGYDLPD
EVFDENEKRPS
Ligand information
Ligand ID
3AT
InChI
InChI=1S/C10H16N5O12P3/c11-8-7-9(13-3-12-8)15(4-14-7)10-6(16)1-5(25-10)2-24-29(20,21)27-30(22,23)26-28(17,18)19/h3-6,10,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19)/t5-,6+,10+/m0/s1
InChIKey
NLIHPCYXRYQPSD-BAJZRUMYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)C[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3
OpenEye OEToolkits 1.7.5
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H](C[C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O)N
CACTVS 3.385
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)C[C@H]3O
OpenEye OEToolkits 1.7.5
c1nc(c2c(n1)n(cn2)C3C(CC(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)N
Formula
C10 H16 N5 O12 P3
Name
3'-DEOXYADENOSINE-5'-TRIPHOSPHATE;
CORDYCEPIN TRIPHOSPHATE
ChEMBL
CHEMBL480329
DrugBank
DB01860
ZINC
ZINC000013540909
PDB chain
1fa0 Chain B Residue 605 [
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Receptor-Ligand Complex Structure
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PDB
1fa0
Structure of yeast poly(A) polymerase alone and in complex with 3'-dATP.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
S89 S99 D100 D102 F140 V234
Binding residue
(residue number reindexed from 1)
S88 S98 D99 D101 F139 V233
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S89 D100 D102 D154 K215 Y224
Catalytic site (residue number reindexed from 1)
S88 D99 D101 D153 K214 Y223
Enzyme Commision number
2.7.7.19
: polynucleotide adenylyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003723
RNA binding
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016740
transferase activity
GO:0016779
nucleotidyltransferase activity
GO:0046872
metal ion binding
GO:1990817
poly(A) RNA polymerase activity
Biological Process
GO:0006397
mRNA processing
GO:0030846
termination of RNA polymerase II transcription, poly(A)-coupled
GO:0031123
RNA 3'-end processing
GO:0031124
mRNA 3'-end processing
GO:0031126
sno(s)RNA 3'-end processing
Cellular Component
GO:0005634
nucleus
GO:0005847
mRNA cleavage and polyadenylation specificity factor complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1fa0
,
PDBe:1fa0
,
PDBj:1fa0
PDBsum
1fa0
PubMed
10958780
UniProt
P29468
|PAP_YEAST Poly(A) polymerase (Gene Name=PAP1)
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