Structure of PDB 1t2a Chain B Binding Site BS01
Receptor Information
>1t2a Chain B (length=338) Species:
9606
(Homo sapiens) [
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RNVALITGITGQDGSYLAEFLLEKGYEVHGIVRRSSSFNTGRIEHLYNMK
LHYGDLTDSTCLVKIINEVKPTEIYNLGAQSHVKISFDLAEYTADVDGVG
TLRLLDAVKTCGLINSVKFYQASTSELYGKVQEIPQKETTPFYPRSPYGA
AKLYAYWIVVNFREAYNLFAVNGILFNHESPRRGANFVTRKISRSVAKIY
LGQLECFSLGNLDAKRDWGHAKDYVEAMWLMLQNDEPEDFVIATGEVHSV
REFVEKSFLHIGKTIVWEGKNENEVGRCKETGKVHVTVDLKYYRPTEVDF
LQGDCTKAKQKLNWKPRVAFDELVREMVHADVELMRTN
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-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)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
1t2a Chain B Residue 1101 [
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Receptor-Ligand Complex Structure
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PDB
1t2a
Crystal Structure and Biophysical Characterization of Human GDP-D-mannose 4,6-dehydratase
Resolution
1.84 Å
Binding residue
(original residue number in PDB)
G30 T32 G33 Q34 D35 R55 D86 L87 L108 G109 A110 S112 V127 A153 S154 T155 Y179 K183 L206 N208 H209 R214
Binding residue
(residue number reindexed from 1)
G8 T10 G11 Q12 D13 R33 D55 L56 L77 G78 A79 S81 V96 A122 S123 T124 Y148 K152 L175 N177 H178 R183
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T155 S156 E157 Y179 K183
Catalytic site (residue number reindexed from 1)
T124 S125 E126 Y148 K152
Enzyme Commision number
4.2.1.47
: GDP-mannose 4,6-dehydratase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008446
GDP-mannose 4,6-dehydratase activity
GO:0016829
lyase activity
GO:0042802
identical protein binding
GO:0070401
NADP+ binding
Biological Process
GO:0007219
Notch signaling pathway
GO:0019673
GDP-mannose metabolic process
GO:0042350
GDP-L-fucose biosynthetic process
GO:0042351
'de novo' GDP-L-fucose biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0070062
extracellular exosome
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1t2a
,
PDBe:1t2a
,
PDBj:1t2a
PDBsum
1t2a
PubMed
UniProt
O60547
|GMDS_HUMAN GDP-mannose 4,6 dehydratase (Gene Name=GMDS)
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