4YLJ

Crystal structure of DYRK1A in complex with 10-Iodo-substituted 11H-indolo[3,2-c]quinoline-6-carboxylic acid inhibitor 5j

Functional Information from GO Data

Chain	GOid	namespace	contents
A	0004672	molecular_function	protein kinase activity
A	0004712	molecular_function	protein serine/threonine/tyrosine kinase activity
A	0005524	molecular_function	ATP binding
A	0006468	biological_process	protein phosphorylation
A	0046777	biological_process	protein autophosphorylation
B	0004672	molecular_function	protein kinase activity
B	0004712	molecular_function	protein serine/threonine/tyrosine kinase activity
B	0005524	molecular_function	ATP binding
B	0006468	biological_process	protein phosphorylation
B	0046777	biological_process	protein autophosphorylation
C	0004672	molecular_function	protein kinase activity
C	0004712	molecular_function	protein serine/threonine/tyrosine kinase activity
C	0005524	molecular_function	ATP binding
C	0006468	biological_process	protein phosphorylation
C	0046777	biological_process	protein autophosphorylation
D	0004672	molecular_function	protein kinase activity
D	0004712	molecular_function	protein serine/threonine/tyrosine kinase activity
D	0005524	molecular_function	ATP binding
D	0006468	biological_process	protein phosphorylation
D	0046777	biological_process	protein autophosphorylation

Functional Information from PDB Data

site_id	AC1
Number of Residues	4
Details	binding site for residue PG4 A 501

Chain	Residue
A	ASP162
A	LYS175
A	TRP184
A	MET240

---

site_id	AC2
Number of Residues	2
Details	binding site for residue PG4 A 502

Chain	Residue
A	TYR319
A	HOH642

---

site_id	AC3
Number of Residues	4
Details	binding site for residue SO4 A 503

Chain	Residue
A	ARG438
A	ARG255
A	GLY256
A	SER258

---

site_id	AC4
Number of Residues	5
Details	binding site for residue SO4 A 504

Chain	Residue
A	ARG458
A	ARG467
A	ILE468
A	GLN469
A	TYR472

---

site_id	AC5
Number of Residues	11
Details	binding site for residue 4E1 A 505

Chain	Residue
A	GLY166
A	LYS167
A	PHE170
A	VAL173
A	ALA186
A	LYS188
A	PHE238
A	MET240
A	VAL306
A	ASP307
A	HOH660

---

site_id	AC6
Number of Residues	4
Details	binding site for residue PG4 B 501

Chain	Residue
B	GLN201
B	LEU234
D	GLN201
D	LEU234

---

site_id	AC7
Number of Residues	3
Details	binding site for residue PG4 B 502

Chain	Residue
B	ASP162
B	LYS175
B	MET240

---

site_id	AC8
Number of Residues	1
Details	binding site for residue PG4 B 503

Chain	Residue
B	TYR471

---

site_id	AC9
Number of Residues	3
Details	binding site for residue SO4 B 504

Chain	Residue
B	LYS264
B	ARG300
B	SER301

---

site_id	AD1
Number of Residues	4
Details	binding site for residue SO4 B 505

Chain	Residue
B	PTR321
B	ARG325
D	ASN297
D	ARG300

---

site_id	AD2
Number of Residues	2
Details	binding site for residue SO4 B 506

Chain	Residue
B	LYS225
B	ARG226

---

site_id	AD3
Number of Residues	5
Details	binding site for residue SO4 B 507

Chain	Residue
B	THR466
B	ARG467
B	ILE468
B	GLN469
B	TYR472

---

site_id	AD4
Number of Residues	10
Details	binding site for residue 4E1 B 508

Chain	Residue
B	PHE170
B	VAL173
B	ALA186
B	LYS188
B	PHE238
B	GLU239
B	MET240
B	ASP307
B	HOH625
D	GLN182

---

site_id	AD5
Number of Residues	5
Details	binding site for residue PG4 C 501

Chain	Residue
A	GLN201
C	GLN201
C	HIS227
C	MET229
C	HOH603

---

site_id	AD6
Number of Residues	2
Details	binding site for residue SO4 C 502

Chain	Residue
C	ARG300
C	SER301

---

site_id	AD7
Number of Residues	12
Details	binding site for residue 4E1 C 503

Chain	Residue
C	GLY166
C	LYS167
C	PHE170
C	VAL173
C	ALA186
C	LYS188
C	PHE238
C	MET240
C	LEU241
C	LEU294
C	VAL306
C	ASP307

---

site_id	AD8
Number of Residues	5
Details	binding site for residue PG4 D 501

Chain	Residue
D	ASP162
D	LYS175
D	TRP184
D	MET240
D	HOH626

---

site_id	AD9
Number of Residues	5
Details	binding site for residue SO4 D 502

Chain	Residue
D	ARG458
D	ARG467
D	ILE468
D	GLN469
D	TYR472

---

site_id	AE1
Number of Residues	3
Details	binding site for residue SO4 D 503

Chain	Residue
D	LYS225
D	ARG226
D	HOH608

---

site_id	AE2
Number of Residues	3
Details	binding site for residue SO4 D 504

Chain	Residue
D	LYS264
D	ARG300
D	SER301

---

site_id	AE3
Number of Residues	9
Details	binding site for residue 4E1 D 505

Chain	Residue
D	MET240
D	VAL306
D	ASP307
D	LYS167
D	PHE170
D	VAL173
D	ALA186
D	LYS188
D	PHE238

---

Functional Information from PROSITE/UniProt

site_id	PS00107
Number of Residues	24
Details	PROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. IGKGSFGQVVkAydrveqew..........VAIK

Chain	Residue	Details
A	ILE165-LYS188

---

site_id	PS00108
Number of Residues	13
Details	PROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. IiHcDLKpeNILL

Chain	Residue	Details
A	ILE283-LEU295

---

Functional Information from SwissProt/UniProt

site_id	SWS_FT_FI1
Number of Residues	4
Details	ACT_SITE: Proton acceptor => ECO:0000305|PubMed:23665168

Chain	Residue	Details
A	ASP287
B	ASP287
C	ASP287
D	ASP287

---

site_id	SWS_FT_FI2
Number of Residues	12
Details	BINDING: BINDING => ECO:0000305

Chain	Residue	Details
A	ILE165
D	ILE165
D	LYS188
D	PHE238
A	LYS188
A	PHE238
B	ILE165
B	LYS188
B	PHE238
C	ILE165
C	LYS188
C	PHE238

---

site_id	SWS_FT_FI3
Number of Residues	24
Details	MOD_RES: Phosphotyrosine; by autocatalysis => ECO:0000269|PubMed:23665168

Chain	Residue	Details
A	TYR140
B	TYR319
B	PTR321
B	TYR449
C	TYR140
C	TYR159
C	TYR177
C	TYR319
C	PTR321
C	TYR449
D	TYR140
A	TYR159
D	TYR159
D	TYR177
D	TYR319
D	PTR321
D	TYR449
A	TYR177
A	TYR319
A	PTR321
A	TYR449
B	TYR140
B	TYR159
B	TYR177

---

site_id	SWS_FT_FI4
Number of Residues	4
Details	MOD_RES: Phosphotyrosine => ECO:0007744|PubMed:19690332, ECO:0007744|PubMed:23186163

Chain	Residue	Details
A	TYR145
B	TYR145
C	TYR145
D	TYR145

---

site_id	SWS_FT_FI5
Number of Residues	4
Details	MOD_RES: Phosphotyrosine; by autocatalysis => ECO:0000250|UniProtKB:Q63470

Chain	Residue	Details
A	TYR219
B	TYR219
C	TYR219
D	TYR219

---

site_id	SWS_FT_FI6
Number of Residues	4
Details	MOD_RES: Phosphoserine; by autocatalysis => ECO:0000269|PubMed:23665168

Chain	Residue	Details
A	SER310
B	SER310
C	SER310
D	SER310

---

site_id	SWS_FT_FI7
Number of Residues	4
Details	MOD_RES: Phosphothreonine; by autocatalysis => ECO:0000269|PubMed:23665168

Chain	Residue	Details
A	THR402
B	THR402
C	THR402
D	THR402

---