Structure of PDB 2cvx Chain A Binding Site BS01
Receptor Information
>2cvx Chain A (length=664) Species:
4932
(Saccharomyces cerevisiae) [
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TLAARIAISNLHKQTTKQFSKVVEDLYRYVNAATGKPAPMISDDVYNIVM
ENKDKLNSAIVYDRDFQYSYFGFKTLERSYLLRINGQVAERPQHLIMRVA
LGIHGRDIEAALETYNLMSLKYFTHASPTLFNAGTPKPQMSSCFLVAMKE
DSIEGIYDTLKECALISKTAGGIGLHIHNIRSTGSYIAGTNGTSNGLIPM
IRVFNNTARYVDQGGNKRPGAFALYLEPWHADIFDFIDIRKNHGKEEIRA
RDLFPALWIPDLFMKRVEENGTWTLFSPTSAPGLSDCYGDEFEALYTRYE
KEGRGKTIKAQKLWYSILEAQTETGTPFVVYKDACNRKSNQKNLGVIKSS
NLCCEIVEYSAPDETAVCNLASVALPAFIETSEDGKTSTYNFKKLHEIAK
VVTRNLNRVIDRNYYPVEEARKSNMRHRPIALGVQGLADTFMLLRLPFDS
EEARLLNIQIFETIYHASMEASCELAQKDGPYETFQGSPASQGILQFDMW
DQKPYGMWDWDTLRKDIMKHGVRNSLTMAPMPTASTSQILGYNECFEPVT
SNMYSFQVVNPYLLRDLVDLGIWDEGMKQYLITQNGSIQGLPNVPQELKD
LYKTVWEISQKTIINMAADRSVYIDQSHSLNLFLRAPTMGKLTSMHFYGW
KKGLKTGMYYLRTQ
Ligand information
Ligand ID
DGT
InChI
InChI=1S/C10H16N5O13P3/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(26-6)2-25-30(21,22)28-31(23,24)27-29(18,19)20/h3-6,16H,1-2H2,(H,21,22)(H,23,24)(H2,18,19,20)(H3,11,13,14,17)/t4-,5+,6+/m0/s1
InChIKey
HAAZLUGHYHWQIW-KVQBGUIXSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3CC(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)N=C(NC2=O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3C[CH](O)[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)O3
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@H]3C[C@H](O)[C@@H](CO[P@](O)(=O)O[P@](O)(=O)O[P](O)(O)=O)O3
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)CC3O
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3C[C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O)N=C(NC2=O)N
Formula
C10 H16 N5 O13 P3
Name
2'-DEOXYGUANOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL477486
DrugBank
DB02181
ZINC
ZINC000008215755
PDB chain
2cvx Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
2cvx
Structures of eukaryotic ribonucleotide reductase I provide insights into dNTP regulation
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
D226 S227 I228 R256 I262 A263 G264
Binding residue
(residue number reindexed from 1)
D151 S152 I153 R181 I187 A188 G189
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C218 N426 C428 E430 C443 Y741 Y742
Catalytic site (residue number reindexed from 1)
C143 N351 C353 E355 C368 Y659 Y660
Enzyme Commision number
1.17.4.1
: ribonucleoside-diphosphate reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004748
ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
Biological Process
GO:0009263
deoxyribonucleotide biosynthetic process
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005971
ribonucleoside-diphosphate reductase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2cvx
,
PDBe:2cvx
,
PDBj:2cvx
PDBsum
2cvx
PubMed
16537479
UniProt
P21524
|RIR1_YEAST Ribonucleoside-diphosphate reductase large chain 1 (Gene Name=RNR1)
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