2EII
Crystal analysis of delta1-pyrroline-5-carboxylate dehydrogenase from Thermus thermophilus with bound L-valine and NAD.
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000166 | molecular_function | nucleotide binding |
A | 0003842 | molecular_function | L-glutamate gamma-semialdehyde dehydrogenase activity |
A | 0004657 | molecular_function | proline dehydrogenase activity |
A | 0009898 | cellular_component | cytoplasmic side of plasma membrane |
A | 0010133 | biological_process | L-proline catabolic process to L-glutamate |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0016620 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor |
B | 0000166 | molecular_function | nucleotide binding |
B | 0003842 | molecular_function | L-glutamate gamma-semialdehyde dehydrogenase activity |
B | 0004657 | molecular_function | proline dehydrogenase activity |
B | 0009898 | cellular_component | cytoplasmic side of plasma membrane |
B | 0010133 | biological_process | L-proline catabolic process to L-glutamate |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0016620 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE ACT A 1519 |
Chain | Residue |
A | ALA245 |
A | GLU249 |
A | ILE268 |
A | ALA271 |
A | NAD1518 |
A | HOH2863 |
site_id | AC2 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ACT A 1520 |
Chain | Residue |
A | HOH2790 |
B | LYS510 |
A | ARG462 |
A | PHE464 |
A | HIS465 |
site_id | AC3 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE NA A 1540 |
Chain | Residue |
A | SER55 |
A | LEU56 |
A | GLU123 |
A | ASP211 |
A | HOH2701 |
A | HOH2813 |
site_id | AC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE ACT B 2519 |
Chain | Residue |
B | ALA245 |
B | GLU249 |
B | ILE268 |
B | ALA271 |
B | NAD2518 |
B | HOH2979 |
site_id | AC5 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE ACT B 2520 |
Chain | Residue |
A | LYS510 |
B | ARG462 |
B | PHE464 |
B | HIS465 |
B | HOH2749 |
B | HOH2829 |
site_id | AC6 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE NA B 2540 |
Chain | Residue |
B | SER55 |
B | LEU56 |
B | GLU123 |
B | ASP211 |
B | HOH2857 |
B | HOH2872 |
site_id | AC7 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE VAL A 1517 |
Chain | Residue |
A | GLU137 |
A | PHE185 |
A | CYS322 |
A | SER323 |
A | GLY477 |
A | ALA478 |
A | PHE485 |
A | HOH2563 |
A | HOH2660 |
A | HOH3025 |
A | HOH3026 |
site_id | AC8 |
Number of Residues | 35 |
Details | BINDING SITE FOR RESIDUE NAD A 1518 |
Chain | Residue |
A | ILE180 |
A | ALA181 |
A | PRO182 |
A | TRP183 |
A | ASN184 |
A | ILE189 |
A | LYS207 |
A | ALA209 |
A | GLU210 |
A | GLY240 |
A | GLU241 |
A | GLY244 |
A | ALA245 |
A | PHE258 |
A | THR259 |
A | GLY260 |
A | SER261 |
A | VAL264 |
A | GLU288 |
A | THR289 |
A | GLY290 |
A | CYS322 |
A | GLU417 |
A | PHE419 |
A | LEU445 |
A | PHE485 |
A | ACT1519 |
A | HOH2639 |
A | HOH2828 |
A | HOH2845 |
A | HOH2862 |
A | HOH3002 |
A | HOH3031 |
A | HOH3032 |
A | HOH3034 |
site_id | AC9 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE VAL B 2517 |
Chain | Residue |
B | GLU137 |
B | PHE185 |
B | SER323 |
B | GLY477 |
B | ALA478 |
B | PHE485 |
B | HOH2582 |
B | HOH2664 |
B | HOH3007 |
B | HOH3008 |
site_id | BC1 |
Number of Residues | 32 |
Details | BINDING SITE FOR RESIDUE NAD B 2518 |
Chain | Residue |
B | GLU210 |
B | GLY240 |
B | GLY244 |
B | ALA245 |
B | PHE258 |
B | THR259 |
B | GLY260 |
B | SER261 |
B | VAL264 |
B | GLU288 |
B | THR289 |
B | GLY290 |
B | CYS322 |
B | GLU417 |
B | PHE419 |
B | LEU445 |
B | PHE485 |
B | ACT2519 |
B | HOH2650 |
B | HOH2653 |
B | HOH2767 |
B | HOH2768 |
B | HOH2847 |
B | HOH3006 |
B | ILE180 |
B | ALA181 |
B | PRO182 |
B | TRP183 |
B | ASN184 |
B | ILE189 |
B | LYS207 |
B | ALA209 |
site_id | BC2 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE MPD B 1530 |
Chain | Residue |
A | GLU158 |
B | PHE6 |
B | TYR144 |
B | ALA148 |
B | HOH2604 |
B | HOH2616 |
B | HOH2655 |
B | HOH2866 |
site_id | BC3 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE MPD A 1531 |
Chain | Residue |
A | ASP359 |
A | HOH2607 |
site_id | BC4 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE MPD A 1532 |
Chain | Residue |
A | LEU275 |
A | GLN279 |
A | HOH2706 |
A | HOH2999 |
B | MPD2535 |
site_id | BC5 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE MPD A 1533 |
Chain | Residue |
A | TYR171 |
B | HOH2810 |
site_id | BC6 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE MPD B 1534 |
Chain | Residue |
B | LEU275 |
B | GLN279 |
B | HOH2733 |
B | HOH2913 |
site_id | BC7 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE MPD B 1535 |
Chain | Residue |
A | PHE170 |
B | PRO94 |
B | ARG462 |
B | HOH2732 |
B | HOH2997 |
site_id | BC8 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE MPD A 1536 |
Chain | Residue |
A | ARG36 |
A | TYR38 |
A | PRO39 |
A | TRP46 |
site_id | BC9 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE MPD A 2530 |
Chain | Residue |
A | PHE6 |
A | TYR144 |
A | ALA148 |
A | HOH2614 |
A | HOH2622 |
A | HOH2749 |
B | GLU158 |
site_id | CC1 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE MPD B 2531 |
Chain | Residue |
B | ARG36 |
B | GLU221 |
site_id | CC2 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE MPD B 2532 |
Chain | Residue |
A | LEU27 |
A | ARG28 |
A | TYR122 |
A | GLU355 |
B | PRO353 |
B | GLU355 |
B | GLU356 |
B | HOH2659 |
B | HOH2898 |
site_id | CC3 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE MPD B 2533 |
Chain | Residue |
A | PRO94 |
A | ARG462 |
A | HOH2694 |
A | HOH2848 |
B | TYR154 |
B | PHE170 |
site_id | CC4 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE MPD B 2534 |
Chain | Residue |
B | ARG151 |
site_id | CC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE MPD B 2535 |
Chain | Residue |
A | MPD1532 |
B | GLU416 |
B | HOH2565 |
B | HOH2722 |
site_id | CC6 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE MPD B 2536 |
Chain | Residue |
B | VAL312 |
B | TYR315 |
B | GLY316 |
B | ASP359 |
B | HOH2651 |
Functional Information from PROSITE/UniProt
site_id | PS00070 |
Number of Residues | 12 |
Details | ALDEHYDE_DEHYDR_CYS Aldehyde dehydrogenases cysteine active site. YgFQGQKCSAAS |
Chain | Residue | Details |
A | TYR315-SER326 |
site_id | PS00687 |
Number of Residues | 8 |
Details | ALDEHYDE_DEHYDR_GLU Aldehyde dehydrogenases glutamic acid active site. VETGGKDA |
Chain | Residue | Details |
A | VAL287-ALA294 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1a4s |
Chain | Residue | Details |
A | CYS322 | |
A | ASN184 | |
A | GLU288 |
site_id | CSA2 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1a4s |
Chain | Residue | Details |
B | CYS322 | |
B | ASN184 | |
B | GLU288 |