8S6B
CryoEM structure of Apo form of catalytic domain of human HMG-CoA reductase
Functional Information from PROSITE/UniProt
site_id | PS00066 |
Number of Residues | 15 |
Details | HMG_COA_REDUCTASE_1 Hydroxymethylglutaryl-coenzyme A reductases signature 1. RfQSrSGDaMGmNmI |
Chain | Residue | Details |
A | ARG646-ILE660 |
site_id | PS00318 |
Number of Residues | 8 |
Details | HMG_COA_REDUCTASE_2 Hydroxymethylglutaryl-coenzyme A reductases signature 2. IGtVGGGT |
Chain | Residue | Details |
A | ILE802-THR809 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 3 |
Details | Active site: {"description":"Charge relay system","evidences":[{"source":"PubMed","id":"10698924","evidenceCode":"ECO:0000303"},{"source":"PubMed","id":"11349148","evidenceCode":"ECO:0000303"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 18 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"11349148","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1DQA","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
Catalytic Information from CSA
site_id | MCSA1 |
Number of Residues | 3 |
Details | M-CSA 93 |
Chain | Residue | Details |
A | GLU559 | electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
A | LYS691 | electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor |
A | ASP767 | activator, electrostatic stabiliser, hydrogen bond acceptor |