3MVZ
X-ray structure of the (hydro)peroxo intermediate NikA/1-Int", after monohydroxylation of the iron complex
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0005515 | molecular_function | protein binding |
A | 0015675 | biological_process | nickel cation transport |
A | 0015833 | biological_process | peptide transport |
A | 0016020 | cellular_component | membrane |
A | 0016151 | molecular_function | nickel cation binding |
A | 0020037 | molecular_function | heme binding |
A | 0030288 | cellular_component | outer membrane-bounded periplasmic space |
A | 0042597 | cellular_component | periplasmic space |
A | 0043190 | cellular_component | ATP-binding cassette (ABC) transporter complex |
A | 0046914 | molecular_function | transition metal ion binding |
A | 0050919 | biological_process | negative chemotaxis |
A | 0051540 | molecular_function | metal cluster binding |
A | 0055052 | cellular_component | ATP-binding cassette (ABC) transporter complex, substrate-binding subunit-containing |
A | 0055085 | biological_process | transmembrane transport |
A | 0098716 | biological_process | nickel cation import across plasma membrane |
A | 1904680 | molecular_function | peptide transmembrane transporter activity |
B | 0005515 | molecular_function | protein binding |
B | 0015675 | biological_process | nickel cation transport |
B | 0015833 | biological_process | peptide transport |
B | 0016020 | cellular_component | membrane |
B | 0016151 | molecular_function | nickel cation binding |
B | 0020037 | molecular_function | heme binding |
B | 0030288 | cellular_component | outer membrane-bounded periplasmic space |
B | 0042597 | cellular_component | periplasmic space |
B | 0043190 | cellular_component | ATP-binding cassette (ABC) transporter complex |
B | 0046914 | molecular_function | transition metal ion binding |
B | 0050919 | biological_process | negative chemotaxis |
B | 0051540 | molecular_function | metal cluster binding |
B | 0055052 | cellular_component | ATP-binding cassette (ABC) transporter complex, substrate-binding subunit-containing |
B | 0055085 | biological_process | transmembrane transport |
B | 0098716 | biological_process | nickel cation import across plasma membrane |
B | 1904680 | molecular_function | peptide transmembrane transporter activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ACT A 503 |
Chain | Residue |
A | LYS52 |
A | ARG68 |
A | ASP69 |
A | HOH622 |
site_id | AC2 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE ACT A 504 |
Chain | Residue |
A | ASN261 |
A | LEU263 |
A | HOH727 |
site_id | AC3 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ACT A 505 |
Chain | Residue |
A | PHE419 |
A | GLN423 |
A | HOH914 |
A | ASN235 |
A | ALA237 |
site_id | AC4 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE ACT A 506 |
Chain | Residue |
A | ASN482 |
A | GLN496 |
site_id | AC5 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE SO4 A 507 |
Chain | Residue |
A | ARG384 |
A | HOH854 |
A | HOH861 |
B | LEU430 |
B | ARG457 |
B | HOH568 |
site_id | AC6 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE GOL A 508 |
Chain | Residue |
A | LEU167 |
A | GLN168 |
A | HOH660 |
B | THR211 |
B | ASP213 |
site_id | AC7 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE GOL A 509 |
Chain | Residue |
A | ASN149 |
A | LYS157 |
site_id | AC8 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE GOL A 510 |
Chain | Residue |
A | GLN361 |
A | ASP370 |
A | VAL371 |
A | SER372 |
A | LEU373 |
B | ASN149 |
B | LYS157 |
B | HOH582 |
B | HOH782 |
site_id | AC9 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE FE A 511 |
Chain | Residue |
A | BHN512 |
A | PER513 |
site_id | BC1 |
Number of Residues | 13 |
Details | BINDING SITE FOR RESIDUE BHN A 512 |
Chain | Residue |
A | TYR22 |
A | MET27 |
A | ARG97 |
A | TRP100 |
A | ARG137 |
A | TRP398 |
A | HIS416 |
A | THR490 |
A | FE511 |
A | PER513 |
A | HOH607 |
A | HOH676 |
A | HOH720 |
site_id | BC2 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE PER A 513 |
Chain | Residue |
A | ARG137 |
A | FE511 |
A | BHN512 |
site_id | BC3 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE GOL A 514 |
Chain | Residue |
A | ASN220 |
A | GLU247 |
A | THR490 |
A | GOL521 |
A | HOH548 |
A | HOH928 |
site_id | BC4 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE GOL A 515 |
Chain | Residue |
A | ARG89 |
A | LEU92 |
A | ARG95 |
A | ILE107 |
A | VAL108 |
A | ASP109 |
A | VAL110 |
A | ASN281 |
A | HOH728 |
site_id | BC5 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE GOL A 516 |
Chain | Residue |
A | GLU102 |
A | ASN105 |
A | LYS123 |
A | THR228 |
A | ARG231 |
A | HOH584 |
site_id | BC6 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL A 517 |
Chain | Residue |
A | VAL273 |
A | ASN274 |
A | LYS275 |
A | LYS276 |
A | GLN309 |
A | TYR310 |
A | HOH922 |
A | HOH1120 |
site_id | BC7 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL A 518 |
Chain | Residue |
A | GLU82 |
A | ARG89 |
A | PRO144 |
A | PHE147 |
A | HIS150 |
A | HOH763 |
A | HOH959 |
A | HOH1203 |
site_id | BC8 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE GOL A 519 |
Chain | Residue |
A | ASN302 |
A | GLY304 |
A | HOH900 |
B | PHE229 |
B | ALA230 |
B | SER233 |
site_id | BC9 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE ACT A 520 |
Chain | Residue |
A | HOH646 |
A | THR23 |
A | GLN26 |
site_id | CC1 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE GOL A 521 |
Chain | Residue |
A | TRP10 |
A | GLY219 |
A | ASN220 |
A | GLY222 |
A | LEU223 |
A | GOL514 |
site_id | CC2 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ACT A 522 |
Chain | Residue |
A | ASP331 |
A | ARG365 |
A | HOH1105 |
B | LYS148 |
site_id | CC3 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE ACT A 523 |
Chain | Residue |
A | THR441 |
A | HIS442 |
A | ASP443 |
site_id | CC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE ACT B 503 |
Chain | Residue |
B | THR23 |
B | GLN26 |
B | GLU378 |
B | PER508 |
B | HOH626 |
B | HOH697 |
site_id | CC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ACT B 504 |
Chain | Residue |
B | VAL273 |
B | LYS275 |
B | LYS276 |
B | TYR310 |
site_id | CC6 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE GOL B 505 |
Chain | Residue |
B | TRP10 |
B | PRO11 |
B | GLY219 |
B | ASN220 |
B | GLY222 |
B | LEU223 |
B | GOL509 |
site_id | CC7 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE FE B 506 |
Chain | Residue |
B | BHN507 |
B | PER508 |
site_id | CC8 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE BHN B 507 |
Chain | Residue |
B | TYR22 |
B | MET27 |
B | ARG97 |
B | TRP100 |
B | ARG137 |
B | TRP398 |
B | THR490 |
B | FE506 |
B | PER508 |
B | HOH635 |
B | HOH1202 |
site_id | CC9 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE PER B 508 |
Chain | Residue |
B | ARG137 |
B | ACT503 |
B | FE506 |
B | BHN507 |
site_id | DC1 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL B 509 |
Chain | Residue |
B | ASN220 |
B | GLU247 |
B | ARG396 |
B | MET472 |
B | ALA489 |
B | THR490 |
B | GOL505 |
B | HOH577 |
site_id | DC2 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL B 510 |
Chain | Residue |
A | LEU21 |
A | TYR22 |
A | THR23 |
A | ARG97 |
A | HOH644 |
A | HOH748 |
B | LYS314 |
B | HOH657 |
site_id | DC3 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE GOL B 511 |
Chain | Residue |
A | ASP43 |
A | PRO299 |
B | GLN241 |
B | ASN482 |
B | ILE483 |
B | PRO484 |
B | TYR485 |
B | HOH526 |
B | HOH695 |
site_id | DC4 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL B 512 |
Chain | Residue |
B | GLU221 |
B | VAL249 |
B | SER353 |
B | MET356 |
B | PHE394 |
B | ARG396 |
B | HOH848 |
B | HOH1114 |
Functional Information from PROSITE/UniProt
site_id | PS01040 |
Number of Residues | 23 |
Details | SBP_BACTERIAL_5 Bacterial extracellular solute-binding proteins, family 5 signature. AkswthseDgkTWtFtLRDDVKF |
Chain | Residue | Details |
A | ALA51-PHE73 |