Structure of PDB 3rv3 Chain A Binding Site BS02
Receptor Information
>3rv3 Chain A (length=447) Species:
83333
(Escherichia coli K-12) [
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GSHMLDKIVIANRGEIALRILRACKELGIKTVAVHSSADRDLKHVLLADE
TVCIGPAPSVKSYLNIPAIISAAEITGAVAIHPGYGFLSENANFAEQVER
SGFIFIGPKAETIRLMGDKVSAIAAMKKAGVPCVPGSDGPLGDDMDKNRA
IAKRIGYPVIIKASGGGGGRGMRVVRGDAELAQSISMTRAEAKAAFSNDM
VYMEKYLENPRHVEIQVLADGQGNAIYLAERDCSMQRRHQKVVEEAPAPG
ITPELRRYIGERCAKACVDIGYRGAGTFEFLFENGEFYFIEMNTRIQVEH
PVTEMITGVDLIKEQLRIAAGQPLSIKQEEVHVRGHAVECRINAEDPNTF
LPSPGKITRFHAPGGFGVRWESHIYAGYTVPPYYDSMIGKLICYGENRDV
AIARMKNALQELIIDGIKTNVDLQIRIMNDENFQHGGTNIHYLEKKL
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-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)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[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)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
3rv3 Chain A Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
3rv3
Structural and biochemical studies on the regulation of biotin carboxylase by substrate inhibition and dimerization.
Resolution
1.91 Å
Binding residue
(original residue number in PDB)
K116 K159 G164 G165 G166 M169 E201 K202 Y203 L204 H209 Q233 H236 L278 E288 I437
Binding residue
(residue number reindexed from 1)
K119 K162 G167 G168 G169 M172 E204 K205 Y206 L207 H212 Q236 H239 L281 E291 I440
Annotation score
5
Binding affinity
PDBbind-CN
: -logKd/Ki=2.00,IC50=10mM
Enzymatic activity
Catalytic site (original residue number in PDB)
K116 K159 D196 H209 R235 T274 E276 E288 N290 R292 E296 R338
Catalytic site (residue number reindexed from 1)
K119 K162 D199 H212 R238 T277 E279 E291 N293 R295 E299 R341
Enzyme Commision number
6.3.4.14
: biotin carboxylase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003989
acetyl-CoA carboxylase activity
GO:0004075
biotin carboxylase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016874
ligase activity
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
Biological Process
GO:0006633
fatty acid biosynthetic process
GO:0045717
negative regulation of fatty acid biosynthetic process
GO:2001295
malonyl-CoA biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0009317
acetyl-CoA carboxylase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3rv3
,
PDBe:3rv3
,
PDBj:3rv3
PDBsum
3rv3
PubMed
21592965
UniProt
P24182
|ACCC_ECOLI Biotin carboxylase (Gene Name=accC)
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