Structure of PDB 1pj4 Chain A Binding Site BS02
Receptor Information
>1pj4 Chain A (length=552) Species:
9606
(Homo sapiens) [
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KEKGKPLMLNPRTNKGMAFTLQERQMLGLQGLLPPKIETQDIQALRFHRN
LKKMTSPLEKYIYIMGIQERNEKLFYRILQDDIESLMPIVYTPTVGLACS
QYGHIFRRPKGLFISISDRGHVRSIVDNWPENHVKAVVVTDGERILGLGD
LGVYGMGIPVGKLCLYTACAGIRPDRCLPVCIDVGTDNIALLKDPFYMGL
YQKRDRTQQYDDLIDEFMKAITDRYGRNTLIQFEDFGNHNAFRFLRKYRE
KYCTFNDDIQGTAAVALAGLLAAQKVISKPISEHKILFLGAGEAALGIAN
LIVMSMVENGLSEQEAQKKIWMFDKYGLLVKGRKAKIDSYQEPFTHSAPE
SIPDTFEDAVNILKPSTIIGVAGAGRLFTPDVIRAMASINERPVIFALSN
PTAQAECTAEEAYTLTEGRCLFASGSPFGPVKLTDGRVFTPGQGNNVYIF
PGVALAVILCNTRHISDSVFLEAAKALTSQLTDEELAQGRLYPPLANIQE
VSINIAIKVTEYLYANKMAFRYPEPEDKAKYVKERTWRSEYDSLLPDVYE
WP
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=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[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
1pj4 Chain A Residue 4601 [
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Receptor-Ligand Complex Structure
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PDB
1pj4
Crystal structures of substrate complexes of malic enzyme and insights into the catalytic mechanism.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
R165 N259 A312 G313 E314 A315 D345 K346 V392 A393 G394
Binding residue
(residue number reindexed from 1)
R144 N238 A291 G292 E293 A294 D324 K325 V371 A372 G373
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
Y112 R165 K183 E255 D256 D278 D279 N421
Catalytic site (residue number reindexed from 1)
Y91 R144 K162 E234 D235 D257 D258 N400
Enzyme Commision number
1.1.1.38
: malate dehydrogenase (oxaloacetate-decarboxylating).
Gene Ontology
Molecular Function
GO:0004470
malic enzyme activity
GO:0004471
malate dehydrogenase (decarboxylating) (NAD+) activity
GO:0004473
malate dehydrogenase (decarboxylating) (NADP+) activity
GO:0008948
oxaloacetate decarboxylase activity
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0046872
metal ion binding
GO:0051287
NAD binding
Biological Process
GO:0006090
pyruvate metabolic process
GO:0006108
malate metabolic process
GO:1902031
regulation of NADP metabolic process
Cellular Component
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0043231
intracellular membrane-bounded organelle
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1pj4
,
PDBe:1pj4
,
PDBj:1pj4
PDBsum
1pj4
PubMed
12962632
UniProt
P23368
|MAOM_HUMAN NAD-dependent malic enzyme, mitochondrial (Gene Name=ME2)
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