Structure of PDB 1gz3 Chain D Binding Site BS01
Receptor Information
>1gz3 Chain D (length=554) Species:
9606
(Homo sapiens) [
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HIKEKGKPLMLNPRTNKGMAFTLQERQMLGLQGLLPPKIETQDIQALRFH
RNLKKMTSPLEKYIYIMGIQERNEKLFYRILQDDIESLMPIVYTPTVGLA
CSQYGHIFRRPKGLFISISDRGHVRSIVDNWPENHVKAVVVTDGERILGL
GDLGVYGMGIPVGKLCLYTACAGIRPDQCLPVCIDVGTDNIALLKDPFYM
GLYQKRDRTQQYDDLIDEFMKAITDRYGRNTLIQFEDFGNHNAFRFLRKY
REKYCTFNDDIQGTAAVALAGLLAAQKVISKPISEHKILFLGAGEAALGI
ANLIVMSMVENGLSEQEAQKKIWMFDKYGLLVKGRKAKIDSYQEPFTHSA
PESIPDTFEDAVNILKPSTIIGVAGAGRLFTPDVIRAMASINERPVIFAL
SNPTAQAECTAEEAYTLTEGRCLFASGSPFGPVKLTDGRVFTPGQGNNVY
IFPGVALAVILCNTRHISDSVFLEAAKALTSQLTDEELAQGRLYPPLANI
QEVSINIAIKVTEYLYANKMAFVYPEPEDKAKYVKEQTWRSEYDSLLPDV
YEWP
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
1gz3 Chain D Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
1gz3
Molecular Mechanism for the Regulation of Human Mitochondrial Nad(P)+-Dependent Malic Enzyme by ATP and Fumarate
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
R165 N259 A312 G313 E314 A315 D345 K346 A393 L398
Binding residue
(residue number reindexed from 1)
R146 N240 A293 G294 E295 A296 D326 K327 A374 L379
Annotation score
3
Binding affinity
MOAD
: Ki=0.2mM
Enzymatic activity
Catalytic site (original residue number in PDB)
Y112 R165 K183 E255 D256 D278 D279 N421
Catalytic site (residue number reindexed from 1)
Y93 R146 K164 E236 D237 D259 D260 N402
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:1gz3
,
PDBe:1gz3
,
PDBj:1gz3
PDBsum
1gz3
PubMed
12121650
UniProt
P23368
|MAOM_HUMAN NAD-dependent malic enzyme, mitochondrial (Gene Name=ME2)
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