1U2O
Crystal Structure Of The N-Domain Of Grp94 Lacking The Charged Domain In Complex With Neca
Replaces: 1QYHFunctional Information from GO Data
Chain | GOid | namespace | contents |
A | 0005524 | molecular_function | ATP binding |
A | 0006457 | biological_process | protein folding |
A | 0016887 | molecular_function | ATP hydrolysis activity |
A | 0051082 | molecular_function | unfolded protein binding |
A | 0140662 | molecular_function | ATP-dependent protein folding chaperone |
B | 0005524 | molecular_function | ATP binding |
B | 0006457 | biological_process | protein folding |
B | 0016887 | molecular_function | ATP hydrolysis activity |
B | 0051082 | molecular_function | unfolded protein binding |
B | 0140662 | molecular_function | ATP-dependent protein folding chaperone |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 14 |
Details | BINDING SITE FOR RESIDUE NEC A 1001 |
Chain | Residue |
A | ALA111 |
A | HOH2015 |
A | HOH2039 |
A | HOH2059 |
A | HOH2065 |
A | HOH2079 |
A | ASP149 |
A | MET154 |
A | ASN162 |
A | GLY196 |
A | VAL197 |
A | TYR200 |
A | HOH2004 |
A | HOH2009 |
site_id | AC2 |
Number of Residues | 15 |
Details | BINDING SITE FOR RESIDUE NEC B 1002 |
Chain | Residue |
B | ASN107 |
B | ALA111 |
B | ASP149 |
B | MET154 |
B | ASN162 |
B | LEU163 |
B | GLY196 |
B | VAL197 |
B | TYR200 |
B | HOH2012 |
B | HOH2013 |
B | HOH2014 |
B | HOH2069 |
B | HOH2138 |
B | HOH2141 |
site_id | AC3 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE PG4 A 2001 |
Chain | Residue |
A | THR212 |
A | ARG237 |
A | THR246 |
A | THR248 |
A | PG42002 |
A | HOH2085 |
A | HOH2134 |
site_id | AC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE PG4 A 2002 |
Chain | Residue |
A | LYS137 |
A | THR148 |
A | TRP282 |
A | PG42001 |
A | HOH2046 |
A | HOH2134 |
site_id | AC5 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE 1PE B 2006 |
Chain | Residue |
A | ASN83 |
A | MET86 |
A | LYS87 |
A | SER227 |
B | ASN83 |
B | LYS87 |
B | ILE90 |
B | SER227 |
B | HOH2124 |
site_id | AC6 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE PG4 B 2008 |
Chain | Residue |
B | THR212 |
B | ARG237 |
B | THR240 |
B | THR248 |
B | PG42009 |
B | HOH2016 |
B | HOH2072 |
B | HOH2112 |
site_id | AC7 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE PG4 B 2009 |
Chain | Residue |
B | LYS137 |
B | THR148 |
B | TRP282 |
B | PG42008 |
site_id | AC8 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE PG4 B 2011 |
Chain | Residue |
B | GLY128 |
B | ASN129 |
B | ASN239 |
B | GLY242 |
Functional Information from PROSITE/UniProt
site_id | PS00298 |
Number of Residues | 10 |
Details | HSP90 Heat shock hsp90 proteins family signature. YkNKEIFLRE |
Chain | Residue | Details |
A | TYR94-GLU103 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"15292259","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"15951571","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17936703","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1TC0","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1TC6","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1YT0","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2O1U","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2O1V","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 4 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"15292259","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"15951571","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17936703","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1TBW","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1TC0","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1TC6","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1YT0","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2O1U","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2O1V","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"15292259","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"15951571","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17936703","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1TBW","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1TC0","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1TC6","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2O1U","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2O1V","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | Modified residue: {"description":"Phosphoserine","evidences":[{"source":"UniProtKB","id":"Q66HD0","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 4 |
Details | Glycosylation: {"description":"N-linked (GlcNAc...) asparagine","evidences":[{"evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |