Structure of PDB 1xfv Chain F Binding Site BS02
Receptor Information
>1xfv Chain F (length=735) Species:
1392
(Bacillus anthracis) [
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NNLVKTEFTNETLDKIQQTQDLLKKIPKDVLEIYSELGGEIYFTDIDLVE
HKELQDLSEEEKNSMNSRGEKVPFASRFVFEKKRETPKLIINIKDYAINS
EQSKEVYYEIGKGISLDIISKDKSLDPEFLNLIKSLSDDSDSSDLLFSQK
FKEKLELNNKSIDINFIKENLTEFQHAFSLAFSYYFAPDHRTVLELYAPD
MFEYMNKLEKGGFEKISESLKKEGVEKDRIDVLKGEKALKASGLVPEHAD
AFKKIARELNTYILFRPVNKLATNLIKSGVATKGLNVHGKSSDWGPVAGY
IPFDQDLSKKHGQQLAVEKGNLENKKSITEHEGEIGKIPLKLDHLRIEEL
KENGIILKGKKEIDNGKKYYLLESNNQVYEFRISDENNEVQYKTKEGKIT
VLGEKFNWRNIEVMAKNVEGVLKPLTADYDLFALAPSLTEIKKQIPQKEW
DKVVNTPNSLEKQKGVTNLLIKYGIERKPDSTKGTLSNWQKQMLDRLNEA
VKYTGYTGGDVVNHGTEQDNEEFPEKDNEIFIINPEGEFILTKNWEMTGR
FIEKNITGKDYLYYFNRSYNKIAPGNKAYIEWTDPITKAKINTIPTSAEF
IKNLSSIRRSSNVGVYKDSGDKDEFAKKESVKKIAGYLSDYYNSANHIFS
QEKKRKISIFRGIQAYNEIENVLKSKQIAPEYKNYFQYLKERITNQVQLL
LTHQKSNIEFKLLYKQLNFTENETDNFEVFQKIID
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
1xfv Chain F Residue 908 [
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Receptor-Ligand Complex Structure
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PDB
1xfv
Calcium-independent calmodulin binding and two-metal-ion catalytic mechanism of anthrax edema factor.
Resolution
3.35 Å
Binding residue
(original residue number in PDB)
R329 K353 G547 T548 G578
Binding residue
(residue number reindexed from 1)
R266 K290 G484 T485 G515
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
Y626 Y627 R630 Y679 D686
Catalytic site (residue number reindexed from 1)
Y563 Y564 R567 Y616 D623
Enzyme Commision number
4.6.1.1
: adenylate cyclase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008237
metallopeptidase activity
GO:0008294
calcium- and calmodulin-responsive adenylate cyclase activity
GO:0046872
metal ion binding
Cellular Component
GO:0005576
extracellular region
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:1xfv
,
PDBe:1xfv
,
PDBj:1xfv
PDBsum
1xfv
PubMed
15719022
UniProt
P40136
|CYAA_BACAN Calmodulin-sensitive adenylate cyclase (Gene Name=cya)
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