3LDL
Crystal structure of human GRP78 (70kDa heat shock protein 5 / BIP) ATPase domain in complex with ATP
Functional Information from GO Data
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 24 |
Details | BINDING SITE FOR RESIDUE ATP A 408 |
Chain | Residue |
A | GLY36 |
A | GLU293 |
A | LYS296 |
A | ARG297 |
A | SER300 |
A | GLY363 |
A | GLY364 |
A | SER365 |
A | ARG367 |
A | ASP391 |
A | HOH443 |
A | THR37 |
A | HOH448 |
A | HOH470 |
A | HOH491 |
A | HOH590 |
A | HOH594 |
A | THR38 |
A | TYR39 |
A | GLY226 |
A | GLY227 |
A | GLY228 |
A | THR229 |
A | GLY255 |
site_id | AC2 |
Number of Residues | 30 |
Details | BINDING SITE FOR RESIDUE ATP B 501 |
Chain | Residue |
B | MG1 |
B | GLY36 |
B | THR37 |
B | THR38 |
B | TYR39 |
B | GLY226 |
B | GLY227 |
B | GLY228 |
B | THR229 |
B | GLY255 |
B | GLU293 |
B | LYS296 |
B | ARG297 |
B | SER300 |
B | GLY363 |
B | GLY364 |
B | SER365 |
B | ARG367 |
B | ILE368 |
B | ASP391 |
B | HOH428 |
B | HOH438 |
B | HOH482 |
B | HOH495 |
B | HOH554 |
B | HOH558 |
B | HOH565 |
B | HOH582 |
B | HOH612 |
B | HOH623 |
site_id | AC3 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE MG B 1 |
Chain | Residue |
B | HOH409 |
B | HOH428 |
B | HOH447 |
B | ATP501 |
B | HOH607 |
Functional Information from PROSITE/UniProt
site_id | PS00297 |
Number of Residues | 8 |
Details | HSP70_1 Heat shock hsp70 proteins family signature 1. IDLGTTyS |
Chain | Residue | Details |
A | ILE33-SER40 |
site_id | PS00329 |
Number of Residues | 14 |
Details | HSP70_2 Heat shock hsp70 proteins family signature 2. VFDLGGGTfdvSLL |
Chain | Residue | Details |
A | VAL222-LEU235 |
site_id | PS01036 |
Number of Residues | 15 |
Details | HSP70_3 Heat shock hsp70 proteins family signature 3. IvLvGGsTRIPkIqQ |
Chain | Residue | Details |
A | ILE359-GLN373 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 310 |
Details | Region: {"description":"Nucleotide-binding (NBD)","evidences":[{"source":"PubMed","id":"28286085","evidenceCode":"ECO:0000303"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 32 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"21526763","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | Modified residue: {"description":"Phosphoserine","evidences":[{"source":"UniProtKB","id":"P06761","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 6 |
Details | Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"P20029","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 2 |
Details | Modified residue: {"description":"3'-nitrotyrosine","evidences":[{"source":"UniProtKB","id":"P20029","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI6 |
Number of Residues | 2 |
Details | Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"P0DMV8","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI7 |
Number of Residues | 2 |
Details | Modified residue: {"description":"N6-acetyllysine; alternate","evidences":[{"source":"UniProtKB","id":"P20029","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI8 |
Number of Residues | 2 |
Details | Cross-link: {"description":"Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2)","evidences":[{"source":"PubMed","id":"25114211","evidenceCode":"ECO:0007744"},{"source":"PubMed","id":"25218447","evidenceCode":"ECO:0007744"},{"source":"PubMed","id":"25755297","evidenceCode":"ECO:0007744"},{"source":"PubMed","id":"28112733","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI9 |
Number of Residues | 4 |
Details | Cross-link: {"description":"Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO1); alternate","evidences":[{"source":"PubMed","id":"25114211","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |