5ORY
Crystal structure of Aurora-A kinase in complex with an allosterically binding fragment
Functional Information from GO Data
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 24 |
Details | binding site for residue ADP A 401 |
Chain | Residue |
A | GLY140 |
A | ALA213 |
A | THR217 |
A | GLU260 |
A | ASN261 |
A | LEU263 |
A | ASP274 |
A | MG402 |
A | MG403 |
A | HOH503 |
A | HOH505 |
A | GLY142 |
A | HOH522 |
A | HOH528 |
A | HOH532 |
A | HOH534 |
A | HOH549 |
A | LYS143 |
A | GLY145 |
A | VAL147 |
A | ALA160 |
A | LYS162 |
A | LEU194 |
A | GLU211 |
site_id | AC2 |
Number of Residues | 5 |
Details | binding site for residue MG A 402 |
Chain | Residue |
A | ASN261 |
A | ASP274 |
A | ADP401 |
A | HOH528 |
A | HOH534 |
site_id | AC3 |
Number of Residues | 6 |
Details | binding site for residue MG A 403 |
Chain | Residue |
A | ASP274 |
A | ADP401 |
A | HOH503 |
A | HOH505 |
A | HOH554 |
A | HOH558 |
site_id | AC4 |
Number of Residues | 2 |
Details | binding site for residue CL A 404 |
Chain | Residue |
A | SER284 |
A | SER284 |
site_id | AC5 |
Number of Residues | 4 |
Details | binding site for residue CL A 405 |
Chain | Residue |
A | ARG255 |
A | ARG286 |
A | ARG286 |
A | THR287 |
site_id | AC6 |
Number of Residues | 6 |
Details | binding site for residue AY4 A 406 |
Chain | Residue |
A | GLU170 |
A | GLU175 |
A | ARG179 |
A | VAL182 |
A | TYR199 |
A | HIS201 |
site_id | AC7 |
Number of Residues | 4 |
Details | binding site for residue CL A 407 |
Chain | Residue |
A | PHE144 |
A | LEU164 |
A | PHE165 |
A | GLN168 |
Functional Information from PROSITE/UniProt
site_id | PS00107 |
Number of Residues | 24 |
Details | PROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGKGKFGNVYlArekqskfi..........LALK |
Chain | Residue | Details |
A | LEU139-LYS162 |
site_id | PS00108 |
Number of Residues | 13 |
Details | PROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. ViHrDIKpeNLLL |
Chain | Residue | Details |
A | VAL252-LEU264 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 1 |
Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PROSITE-ProRule","id":"PRU10027","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"14580337","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 6 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"27837025","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"5G1X","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphothreonine","evidences":[{"source":"PubMed","id":"14580337","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19668197","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphothreonine","evidences":[{"source":"PubMed","id":"11039908","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"13678582","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"14580337","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"16246726","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18662907","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19668197","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"26246606","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphoserine; by PKA and PAK","evidences":[{"source":"PubMed","id":"16246726","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI6 |
Number of Residues | 2 |
Details | Cross-link: {"description":"Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2)","evidences":[{"source":"PubMed","id":"28112733","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |