1N94
Aryl Tetrahydropyridine Inhbitors of Farnesyltransferase: Glycine, Phenylalanine and Histidine Derivates
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0008318 | molecular_function | protein prenyltransferase activity |
A | 0018342 | biological_process | protein prenylation |
B | 0003824 | molecular_function | catalytic activity |
B | 0004311 | molecular_function | farnesyltranstransferase activity |
B | 0004659 | molecular_function | prenyltransferase activity |
B | 0004660 | molecular_function | protein farnesyltransferase activity |
B | 0005515 | molecular_function | protein binding |
B | 0005875 | cellular_component | microtubule associated complex |
B | 0005965 | cellular_component | protein farnesyltransferase complex |
B | 0006629 | biological_process | lipid metabolic process |
B | 0008270 | molecular_function | zinc ion binding |
B | 0008283 | biological_process | cell population proliferation |
B | 0008284 | biological_process | positive regulation of cell population proliferation |
B | 0008285 | biological_process | negative regulation of cell population proliferation |
B | 0008318 | molecular_function | protein prenyltransferase activity |
B | 0014070 | biological_process | response to organic cyclic compound |
B | 0018343 | biological_process | protein farnesylation |
B | 0034097 | biological_process | response to cytokine |
B | 0042060 | biological_process | wound healing |
B | 0042277 | molecular_function | peptide binding |
B | 0045787 | biological_process | positive regulation of cell cycle |
B | 0046872 | molecular_function | metal ion binding |
B | 0048144 | biological_process | fibroblast proliferation |
B | 0048145 | biological_process | regulation of fibroblast proliferation |
B | 0048146 | biological_process | positive regulation of fibroblast proliferation |
B | 0051770 | biological_process | positive regulation of nitric-oxide synthase biosynthetic process |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE ZN B 2 |
Chain | Residue |
B | ASP297 |
B | CYS299 |
B | HIS362 |
site_id | AC2 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE HFP A 501 |
Chain | Residue |
B | ARG202 |
B | HIS248 |
B | GLY250 |
B | CYS254 |
A | TIN1 |
A | LYS164 |
A | TYR166 |
A | ASN199 |
A | TYR200 |
A | HIS201 |
site_id | AC3 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE TIN A 1 |
Chain | Residue |
A | LYS164 |
A | TYR166 |
A | GLN167 |
A | HFP501 |
B | ALA98 |
B | SER99 |
B | TRP106 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 3 |
Details | BINDING: |
Chain | Residue | Details |
B | HIS248 | |
B | ARG291 | |
B | TYR300 |
site_id | SWS_FT_FI2 |
Number of Residues | 3 |
Details | BINDING: BINDING => ECO:0000269|PubMed:18844669, ECO:0000269|PubMed:20056542, ECO:0000269|PubMed:9065406 |
Chain | Residue | Details |
B | ASP297 | |
B | CYS299 | |
B | HIS362 |
site_id | SWS_FT_FI3 |
Number of Residues | 1 |
Details | SITE: Important for selectivity against geranylgeranyl diphosphate => ECO:0000250|UniProtKB:P49356 |
Chain | Residue | Details |
B | TRP102 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1d8d |
Chain | Residue | Details |
A | LYS164 | |
B | TYR300 |
site_id | MCSA1 |
Number of Residues | 9 |
Details | M-CSA 484 |
Chain | Residue | Details |
B | HIS248 | electrostatic stabiliser |
B | ARG291 | electrostatic stabiliser |
B | LYS294 | electrostatic stabiliser |
B | ASP297 | metal ligand |
B | CYS299 | metal ligand |
B | TYR300 | electrostatic stabiliser |
B | ASP352 | metal ligand |
B | ASP359 | electrostatic stabiliser |
B | HIS362 | metal ligand |