Structure of PDB 5l6v Chain C Binding Site BS01
Receptor Information
>5l6v Chain C (length=421) Species:
83333
(Escherichia coli K-12) [
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LMLARQLPLKSVALILAGGRGTRLKDLTNKRAKPAVHFGGKFRIIDFALS
NCINSGIRRMGVITQYQSHTLVQHIQRGWSFFNEEMNEFVDLLPAQQRMK
GENWYRGTADAVTQNLDIIRRYKAEYVVILAGDHIYKQDYSRMLIDHVEK
GARCTVACMPVPIEEASAFGVMAVDENDKIIEFVEKPANPPSMPNDPSKS
LASMGIYVFDADYLYELLEEDDRDENSSHDFGKDLIPKITEAGLAYAHPF
PLSCVQSDPDAEPYWRDVGTLEAYWKANLDLASVVPELDMYDRNWPIRTY
NESLPPAKFVQDRSGSHGMTLNSLVSGGCVISGSVVVQSVLFSRVRVNSF
CNIDSAVLLPEVWVGRSCRLRRCVIDRACVIPEGMVIGENAEEDARRFYR
SEEGIVLVTREMLRKLGHKQE
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
5l6v Chain C Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5l6v
Structural Basis of Glycogen Biosynthesis Regulation in Bacteria.
Resolution
2.667 Å
Binding residue
(original residue number in PDB)
K39 R40 H46 R52 T79 E370 R386 A387 R419
Binding residue
(residue number reindexed from 1)
K30 R31 H37 R43 T70 E361 R377 A378 R410
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.7.7.27
: glucose-1-phosphate adenylyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0005524
ATP binding
GO:0008878
glucose-1-phosphate adenylyltransferase activity
GO:0016208
AMP binding
GO:0016779
nucleotidyltransferase activity
GO:0042802
identical protein binding
Biological Process
GO:0005978
glycogen biosynthetic process
GO:0009058
biosynthetic process
GO:0051289
protein homotetramerization
Cellular Component
GO:0010170
glucose-1-phosphate adenylyltransferase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5l6v
,
PDBe:5l6v
,
PDBj:5l6v
PDBsum
5l6v
PubMed
27545622
UniProt
P0A6V1
|GLGC_ECOLI Glucose-1-phosphate adenylyltransferase (Gene Name=glgC)
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