Structure of PDB 4itr Chain B Binding Site BS01
Receptor Information
>4itr Chain B (length=296) Species:
228400
(Histophilus somni 2336) [
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VNYQDLEDNLNLKGLISLEDDRNANFESNVLKNEKFLDEAREISKKSIPE
ATVKQMSHLPEFDDILTEGAKKVESRINKAITFRPSVEEFSEIQDLVKTL
PKTKVIEDLSTKTNEITEALAATSKTIQRTPELKEQLKTAIEDFLQNSQG
KPLTVQMIENLNHGLRPDEGEGRLLYKKENLTKENAVFSSPEAAKIQLAE
TVDFINRAKNEGIEPSVVGALVYQRLIAYAPFAEGNGRMARVIVNKILLD
AGYPAFTKFSDEFEPQIIPQTKASTKSATSSEVVVEFLKELAKKGS
Ligand information
Ligand ID
AMP
InChI
InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
UDMBCSSLTHHNCD-KQYNXXCUSA-N
SMILES
Software
SMILES
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(O)=O)[CH](O)[CH]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N
ACDLabs 12.01
O=P(O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)O)O)O)N
Formula
C10 H14 N5 O7 P
Name
ADENOSINE MONOPHOSPHATE
ChEMBL
CHEMBL752
DrugBank
DB00131
ZINC
ZINC000003860156
PDB chain
4itr Chain C Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
4itr
Structural basis of Fic-mediated adenylylation.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
E3671 A3673 I3714 N3723 G3724 R3728 I3755 Q3757
Binding residue
(residue number reindexed from 1)
E184 A186 I227 N236 G237 R241 I268 Q270
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.7.7.108
: protein adenylyltransferase.
3.4.22.-
External links
PDB
RCSB:4itr
,
PDBe:4itr
,
PDBj:4itr
PDBsum
4itr
PubMed
20622875
UniProt
Q06277
|IBPA_HISS2 Protein adenylyltransferase and cysteine protease IbpA (Gene Name=ibpA)
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