Structure of PDB 5im3 Chain B Binding Site BS01
Receptor Information
>5im3 Chain B (length=860) Species:
208964
(Pseudomonas aeruginosa PAO1) [
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GQLRVIKRNGTVVPYTDDKITVAITKAFLAVEAAASSRIHDTVRRLTEQV
TATFKRRMPSGGTIHIEEIQDQVELALMRAGEQKVARDYVIYREARAAER
KNASIRITRADGSLSPLDMGRLNTIISEACEGLAEVDGALIERETLKNLY
DGVAEKDVNTALVMTARTLVEREPNYSYVTARLLMDTLRAEALGFLGVAE
SATHHEMAELYAKALPAYIEKGAEFELVDAKLKEFDLEKLGKAIDHERDQ
QFTYLGLQTLYDRYFIHKDGIRFELPQIFFMRVAMGLAIEEKDREARAIE
FYNLLSSFDYMSSTPTLFNAGTLRPQLSSCYLTTVPDDLSGIYGAIHDNA
MLSKFAGGLGNDWTPVRALGSYIKGTNGKSQGVVPFLKVVNDTAVAVNAV
CAYLETWHLDIEEFLELRKNTGDDRRRTHDMNTANWIPDLFMKRVFDDGS
WTLFSPSDVPDLHDLYGKAFEERYEYYEALASYGKLKLHKVVQAKDLWRK
MLSMLFETGHPWLTFKDPCNLRSPQQHVGVVHSSNLCTEITLNTNKDEIA
VCNLGSINLVNHIVDGKLDTAKLEKTVKTAVRMLDNVIDINYYSVPQAQN
SNFKHRPVGLGIMGFQDALYLQHIPYGSDAAIAFADQSMEAISYYAIQAS
CDLADERGAYQTFQGSLWSQGILPIDSEKKLIEERGAKYIEVDLSETLDW
APLRERVQKGIRNSNIMAIAPTATIANITGVSQSIEPTYQNLYVKSNLSG
EFTVINPYLVRDLKARGLWDPVMVNDLKYYDGSVQQIERIPQDLKDLYAT
AFEVETRWIVEAASRRQKWIDQAQSLNLYIAGASGKKLDVTYRMAWFRGL
KTTYYLRALA
Ligand information
Ligand ID
DTP
InChI
InChI=1S/C10H16N5O12P3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(25-7)2-24-29(20,21)27-30(22,23)26-28(17,18)19/h3-7,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1
InChIKey
SUYVUBYJARFZHO-RRKCRQDMSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3C[C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3C[CH](O)[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)O3
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3CC(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[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(n2cnc1c(ncnc12)N)CC3O
Formula
C10 H16 N5 O12 P3
Name
2'-DEOXYADENOSINE 5'-TRIPHOSPHATE
ChEMBL
CHEMBL335538
DrugBank
DB03222
ZINC
ZINC000008215662
PDB chain
5im3 Chain A Residue 1004 [
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Receptor-Ligand Complex Structure
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PDB
5im3
Structural Mechanism of Allosteric Activity Regulation in a Ribonucleotide Reductase with Double ATP Cones.
Resolution
2.298 Å
Binding residue
(original residue number in PDB)
D380 D381 L382 I385 R410 I416 K417
Binding residue
(residue number reindexed from 1)
D337 D338 L339 I342 R367 I373 K374
Annotation score
1
Binding affinity
MOAD
: Kd~1.5uM
Enzymatic activity
Catalytic site (original residue number in PDB)
C373 N585 C587 E589 C602 Y904 Y905
Catalytic site (residue number reindexed from 1)
C330 N535 C537 E539 C552 Y854 Y855
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:0005524
ATP binding
GO:0016491
oxidoreductase activity
Biological Process
GO:0009263
deoxyribonucleotide biosynthetic process
Cellular Component
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:5im3
,
PDBe:5im3
,
PDBj:5im3
PDBsum
5im3
PubMed
27133024
UniProt
Q9I4I1
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