Structure of PDB 4gr5 Chain A Binding Site BS01
Receptor Information
>4gr5 Chain A (length=451) Species:
47763
(Streptomyces lydicus) [
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SNPFEEYDGGHVVLTDALGRHSLWPAGIAVPAGWSVRHGTDSREGCLAHI
EHHWTDLRPTRAPAGACVHELFEAQAARAPDAVALLHEADELTYGALNER
ANRLAHRLVGLGVAPGTLVGVHLERGFDMVVALLAVLKAGGGYTMLDPQF
PVERLALSLEDTGAPLLVTSRPLSGRLTGTTTLYVEDAGNLATGVGPEDV
ACVMFTSGSTGRPKGVMSPHRALTGTYLGQDYAGFGPDEVFLQCSPVSWD
AFGLELFGALLFGARCVLQSGQNPDPLEIGELVARHGVTMLQLSASLFNF
LVDEVPEAFEGVRYAITGGEPASVPHVAKARRDHPALRLGNGYGPAESMG
FTTHHAVVAGDLSGTALPIGVPLAGKRAYVLDDDLKPAANGALGELYVAG
AGLAHGYVSRPALTAERFVADPFAGPGGERMYRTGDLARRRADGVLEYVG
R
Ligand information
Ligand ID
APC
InChI
InChI=1S/C11H18N5O12P3/c12-9-6-10(14-2-13-9)16(3-15-6)11-8(18)7(17)5(27-11)1-26-29(19,20)4-30(21,22)28-31(23,24)25/h2-3,5,7-8,11,17-18H,1,4H2,(H,19,20)(H,21,22)(H2,12,13,14)(H2,23,24,25)/t5-,7-,8-,11-/m1/s1
InChIKey
CAWZRIXWFRFUQB-IOSLPCCCSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(C[P@](=O)(O)OP(=O)(O)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)C[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(CP(=O)(O)OP(=O)(O)O)O)O)O)N
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)CP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)C[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
Formula
C11 H18 N5 O12 P3
Name
DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER;
ALPHA,BETA-METHYLENEADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL132722
DrugBank
DB02596
ZINC
ZINC000008295117
PDB chain
4gr5 Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
4gr5
Structural Basis of the Interaction of MbtH-like Proteins, Putative Regulators of Nonribosomal Peptide Biosynthesis, with Adenylating Enzymes.
Resolution
1.92 Å
Binding residue
(original residue number in PDB)
K227 W262 G332 E333 P334 N354 G355 Y356 P358 E360 D449 Y461 R464
Binding residue
(residue number reindexed from 1)
K214 W249 G319 E320 P321 N341 G342 Y343 P345 E347 D436 Y448 R451
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T219 T239 A359 E360
Catalytic site (residue number reindexed from 1)
T206 T226 A346 E347
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008168
methyltransferase activity
GO:0031177
phosphopantetheine binding
Biological Process
GO:0043041
amino acid activation for nonribosomal peptide biosynthetic process
GO:0044550
secondary metabolite biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4gr5
,
PDBe:4gr5
,
PDBj:4gr5
PDBsum
4gr5
PubMed
23192349
UniProt
D1GLU5
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