Structure of PDB 2pfp Chain A Binding Site BS05
Receptor Information
>2pfp Chain A (length=326) Species:
9606
(Homo sapiens) [
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TNHNLHITEKLEVLAKAYSVQGDKWRALGYAKAINALKSFHKPVTSYQEA
CSIPGIGKRMAEKIIEILESGHLRKLDHISESVPVLELFSNIWGAGTKTA
QMWYQQGFRSLEDIRSQASLTTQQAIGLKHYSDFLERMPREEATEIEQTV
QKAAQAFNSGLLCVACGSYRRGKATCGDVDVLITHPDGRSHRGIFSRLLD
SLRQEGFLTDDLVSQEENGQQQKYLGVCRLPGPGRRHRRLDIIVVPYSEF
ACALLYFTGSAHFNRSMRALAKTKGMSLSEHALSTAVVRNTHGAKVGPGR
VLPTPTEKDVFRLLGLPYREPAERDW
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
2pfp Chain A Residue 755 [
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Receptor-Ligand Complex Structure
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PDB
2pfp
Role of the catalytic metal during polymerization by DNA polymerase lambda.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
R386 G416 S417 R420 G426 D427 D429 Y505 F506 T507 G508 A510 N513
Binding residue
(residue number reindexed from 1)
R137 G167 S168 R171 G177 D178 D180 Y256 F257 T258 G259 A261 N264
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D427 D429 D490
Catalytic site (residue number reindexed from 1)
D178 D180 D241
Enzyme Commision number
2.7.7.7
: DNA-directed DNA polymerase.
4.2.99.-
Gene Ontology
Molecular Function
GO:0003677
DNA binding
GO:0003887
DNA-directed DNA polymerase activity
GO:0016779
nucleotidyltransferase activity
GO:0034061
DNA polymerase activity
Biological Process
GO:0006281
DNA repair
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2pfp
,
PDBe:2pfp
,
PDBj:2pfp
PDBsum
2pfp
PubMed
17475573
UniProt
Q9UGP5
|DPOLL_HUMAN DNA polymerase lambda (Gene Name=POLL)
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