Structure of PDB 3vth Chain A Binding Site BS03
Receptor Information
>3vth Chain A (length=753) Species:
273068
(Caldanaerobacter subterraneus subsp. tengcongensis MB4) [
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RGRVPQIQARQINIFGIVQGVGFRPFVFNIAQKYNLKGIVYNNSSGLYIE
VEGEEKDIEAFIREIKENPPSLSVIDEIQVREVEVKEYKDFKIVGSKEDG
GFVPVSPDMGVCEDCLRELKDPKDRRYRYPFINCTNCGPRFSIIEDIPYD
RAKTSMKVFPMCEKCSREYHDPHDRRFHAQPVACFDCGPSLSFVGEGCFD
DEIKCVAKALKEGKIVAIKGIGGFHLAVNALDDEAVATLRRRKKRYGKPF
AVMMRDVEEVKKYCIVSPEEERLLLSQRRPIVLLKKKGEKLAKGIADDLD
TLGVMLPYAPIHYLLMEEIDFPIVMTSGNVSEEPICKDNEEALEKLKDIA
DVFLLNNRDIVNRIDDSVTSFNAGAERIIRRARGYAPQPILLKKEVKASI
LAVGGFYKNTFCMTKGHYAFISHHIGDLDNEKAFNYYIEQIERYKKLFRV
DPEVVAHDMHKGYLSTQYAKSLDLPKIEVQHHHAHIASCMAEHNLDEKVI
GIAYDGTGYGTDGNVWGAEILVCDLKSFERIAHLKYKPLPGNELAIKKIY
RTALGFIFDNISFYKNFVEQVDSRELDIILKQIDRKINTAYVSSMGRFFD
AVAALIGVRKEVLFEGQAAMELESLMAESEEYYEYEILKEDRYVIDPELI
LRQIYEDYMKGFEKSYISAKFHNTVVNFTYDLANLIRKETGINKVVLSGG
SFQNRYLLRRLIEKLSLSGFEVYSNSKVPCNDGGISLGQAVIANKILEGS
AWS
Ligand information
Ligand ID
APC
InChI
InChI=1S/C11H18N5O12P3/c12-9-6-10(14-2-13-9)16(3-15-6)11-8(18)7(17)5(27-11)1-26-29(19,20)4-30(21,22)28-31(23,24)25/h2-3,5,7-8,11,17-18H,1,4H2,(H,19,20)(H,21,22)(H2,12,13,14)(H2,23,24,25)/t5-,7-,8-,11-/m1/s1
InChIKey
CAWZRIXWFRFUQB-IOSLPCCCSA-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)(C[P@](=O)(O)OP(=O)(O)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)C[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)(CP(=O)(O)OP(=O)(O)O)O)O)O)N
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)CP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)C[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
Formula
C11 H18 N5 O12 P3
Name
DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER;
ALPHA,BETA-METHYLENEADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL132722
DrugBank
DB02596
ZINC
ZINC000008295117
PDB chain
3vth Chain A Residue 804 [
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Receptor-Ligand Complex Structure
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PDB
3vth
Structural basis for the reaction mechanism of S-carbamoylation of HypE by HypF in the maturation of [NiFe]-hydrogenases
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
K245 R247 K250 P251 L285 T303 T328 S329 E334 R382
Binding residue
(residue number reindexed from 1)
K243 R245 K248 P249 L283 T301 T326 S327 E332 R380
Annotation score
3
Enzymatic activity
Enzyme Commision number
3.6.1.7
: acylphosphatase.
6.2.-.-
Gene Ontology
Molecular Function
GO:0003725
double-stranded RNA binding
GO:0003998
acylphosphatase activity
GO:0008270
zinc ion binding
GO:0016743
carboxyl- or carbamoyltransferase activity
GO:0016787
hydrolase activity
GO:0016874
ligase activity
GO:0046872
metal ion binding
Biological Process
GO:0046944
protein carbamoylation
GO:0051604
protein maturation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3vth
,
PDBe:3vth
,
PDBj:3vth
PDBsum
3vth
PubMed
22740694
UniProt
Q8RDB0
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