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5OSF

Crystal structure of Aurora-A kinase in complex with an allosterically binding fragment

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues25
Detailsbinding site for residue ADP A 401
ChainResidue
AGLY140
AGLU211
AALA213
ATHR217
AGLU260
AASN261
ALEU263
AASP274
AMG402
AMG403
AHOH510
AGLY142
AHOH516
AHOH544
AHOH546
AHOH552
AHOH562
AHOH570
ALYS143
APHE144
AGLY145
AVAL147
AALA160
ALYS162
ALEU194

site_idAC2
Number of Residues5
Detailsbinding site for residue MG A 402
ChainResidue
AASN261
AASP274
AADP401
AHOH544
AHOH562

site_idAC3
Number of Residues5
Detailsbinding site for residue MG A 403
ChainResidue
AASP274
AADP401
AHOH516
AHOH524
AHOH579

site_idAC4
Number of Residues4
Detailsbinding site for residue A9E A 404
ChainResidue
ATRP128
APHE133
APHE157
ALEU159

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues24
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGKGKFGNVYlArekqskfi..........LALK
ChainResidueDetails
ALEU139-LYS162

site_idPS00108
Number of Residues13
DetailsPROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. ViHrDIKpeNLLL
ChainResidueDetails
AVAL252-LEU264

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU00159, ECO:0000255|PROSITE-ProRule:PRU10027, ECO:0000269|PubMed:14580337
ChainResidueDetails
AASP256

site_idSWS_FT_FI2
Number of Residues5
DetailsBINDING: BINDING => ECO:0000269|PubMed:27837025, ECO:0007744|PDB:5G1X
ChainResidueDetails
ALYS162
AGLU211
AGLU260
AASP274
ALYS143

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: Phosphothreonine => ECO:0000269|PubMed:14580337, ECO:0000269|PubMed:19668197
ChainResidueDetails
ATHR287

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: Phosphothreonine => ECO:0000269|PubMed:11039908, ECO:0000269|PubMed:13678582, ECO:0000269|PubMed:14580337, ECO:0000269|PubMed:16246726, ECO:0000269|PubMed:18662907, ECO:0000269|PubMed:19668197, ECO:0000269|PubMed:26246606
ChainResidueDetails
ATPO288

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: Phosphoserine; by PKA and PAK => ECO:0000269|PubMed:16246726
ChainResidueDetails
ASER342

site_idSWS_FT_FI6
Number of Residues2
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2) => ECO:0007744|PubMed:28112733
ChainResidueDetails
ALYS258

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PDB entries from 2024-05-29

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