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6POZ

Structure of human endothelial nitric oxide synthase heme domain in complex with 7-(3-(Aminomethyl)-4-isopropoxyphenyl)-4-methylquinolin-2-amine

Functional Information from GO Data
ChainGOidnamespacecontents
A0004517molecular_functionnitric-oxide synthase activity
A0006809biological_processnitric oxide biosynthetic process
B0004517molecular_functionnitric-oxide synthase activity
B0006809biological_processnitric oxide biosynthetic process
C0004517molecular_functionnitric-oxide synthase activity
C0006809biological_processnitric oxide biosynthetic process
D0004517molecular_functionnitric-oxide synthase activity
D0006809biological_processnitric oxide biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues12
Detailsbinding site for residue HEM A 501
ChainResidue
ATRP178
ATYR475
AH4B502
AOSD503
APRO182
AARG183
ACYS184
APHE353
ASER354
ATRP356
AGLU361
ATRP447

site_idAC2
Number of Residues12
Detailsbinding site for residue H4B A 502
ChainResidue
ASER102
AARG365
AALA446
ATRP447
AHEM501
AOSD503
AHOH622
BTRP445
BPHE460
BHIS461
BGLN462
BGLU463

site_idAC3
Number of Residues10
Detailsbinding site for residue OSD A 503
ChainResidue
AVAL104
AVAL336
APHE353
ATRP356
ATYR357
AGLU361
ATRP447
AHEM501
AH4B502
AHOH639

site_idAC4
Number of Residues9
Detailsbinding site for residue BTB A 504
ChainResidue
ATRP322
AVAL381
ACYS382
AASP384
AGD509
AHOH640
DTRP322
DLEU326
DASP378

site_idAC5
Number of Residues3
Detailsbinding site for residue BTB A 505
ChainResidue
AGLU377
AARG388
DASP384

site_idAC6
Number of Residues4
Detailsbinding site for residue ZN A 506
ChainResidue
ACYS94
ACYS99
BCYS94
BCYS99

site_idAC7
Number of Residues2
Detailsbinding site for residue GOL A 507
ChainResidue
AGLU167
AHOH603

site_idAC8
Number of Residues4
Detailsbinding site for residue CL A 508
ChainResidue
AGLN247
AARG250
ATYR357
AASN366

site_idAC9
Number of Residues3
Detailsbinding site for residue GD A 509
ChainResidue
ABTB504
AHOH643
AHOH649

site_idAD1
Number of Residues9
Detailsbinding site for residue OSD A 510
ChainResidue
ATRP74
ATRP445
APHE460
AHOH610
BVAL104
BALA446
BTRP447
BOSD502
BHOH603

site_idAD2
Number of Residues14
Detailsbinding site for residue HEM B 501
ChainResidue
AHOH610
BTRP178
BPRO182
BARG183
BCYS184
BPHE353
BSER354
BTRP356
BGLU361
BTRP447
BTYR475
BOSD502
BHOH604
BHOH606

site_idAD3
Number of Residues8
Detailsbinding site for residue OSD B 502
ChainResidue
AOSD510
BVAL336
BTRP356
BTYR357
BGLU361
BTRP447
BTYR475
BHEM501

site_idAD4
Number of Residues9
Detailsbinding site for residue BTB B 503
ChainResidue
BTHR319
BGLU321
BGD506
BHOH663
CSER260
CVAL261
CTYR373
CASN374
CASP378

site_idAD5
Number of Residues2
Detailsbinding site for residue BTB B 504
ChainResidue
BGLU298
DGLU167

site_idAD6
Number of Residues4
Detailsbinding site for residue CL B 505
ChainResidue
BGLN247
BTYR357
BASN366
BHOH658

site_idAD7
Number of Residues5
Detailsbinding site for residue GD B 506
ChainResidue
BTHR319
BGLU321
BBTB503
BHOH663
CHOH604

site_idAD8
Number of Residues9
Detailsbinding site for residue BTB B 507
ChainResidue
BTRP322
BALA325
BLEU326
BASP378
BHOH652
CVAL381
CCYS382
CASP384
CGD508

site_idAD9
Number of Residues3
Detailsbinding site for residue BTB B 508
ChainResidue
BASP384
CGLU377
CTHR387

site_idAE1
Number of Residues14
Detailsbinding site for residue HEM C 501
ChainResidue
CTRP178
CPRO182
CARG183
CCYS184
CVAL185
CSER226
CPHE353
CSER354
CTRP356
CGLU361
CTRP447
CTYR475
CH4B502
COSD503

site_idAE2
Number of Residues13
Detailsbinding site for residue H4B C 502
ChainResidue
CSER102
CARG365
CALA446
CTRP447
CHEM501
COSD503
CHOH603
CHOH640
CHOH651
DTRP445
DPHE460
DGLN462
DGLU463

site_idAE3
Number of Residues12
Detailsbinding site for residue OSD C 503
ChainResidue
CVAL104
CPHE105
CVAL336
CGLY355
CTRP356
CTYR357
CGLU361
CTYR475
CHEM501
CH4B502
CHOH615
CHOH664

site_idAE4
Number of Residues1
Detailsbinding site for residue BTB C 504
ChainResidue
CGLU298

site_idAE5
Number of Residues4
Detailsbinding site for residue ZN C 505
ChainResidue
CCYS94
CCYS99
DCYS94
DCYS99

site_idAE6
Number of Residues1
Detailsbinding site for residue GOL C 506
ChainResidue
CGLU167

site_idAE7
Number of Residues3
Detailsbinding site for residue CL C 507
ChainResidue
CGLN247
CTYR357
CASN366

site_idAE8
Number of Residues4
Detailsbinding site for residue GD C 508
ChainResidue
BBTB507
BHOH652
BHOH674
CHOH632

site_idAE9
Number of Residues8
Detailsbinding site for residue OSD C 509
ChainResidue
CTRP74
CTRP445
CPHE460
CHOH605
DVAL104
DALA446
DTRP447
DOSD502

site_idAF1
Number of Residues15
Detailsbinding site for residue HEM D 501
ChainResidue
DTRP178
DALA181
DARG183
DCYS184
DVAL185
DSER226
DPHE353
DSER354
DTRP356
DGLU361
DTRP447
DTYR475
DOSD502
DHOH603
DHOH618

site_idAF2
Number of Residues9
Detailsbinding site for residue OSD D 502
ChainResidue
COSD509
DVAL336
DGLY355
DTRP356
DTYR357
DGLU361
DTRP447
DTYR475
DHEM501

site_idAF3
Number of Residues6
Detailsbinding site for residue BTB D 503
ChainResidue
AASP378
DTHR319
DGLU321
DGD505
DHOH605
DHOH629

site_idAF4
Number of Residues3
Detailsbinding site for residue BTB D 504
ChainResidue
BGLU167
DASP297
DGLU298

site_idAF5
Number of Residues5
Detailsbinding site for residue GD D 505
ChainResidue
DTHR319
DGLU321
DBTB503
DHOH605
DHOH629

site_idAF6
Number of Residues4
Detailsbinding site for residue CL D 506
ChainResidue
DGLN247
DARG250
DTYR357
DASN366

Functional Information from PROSITE/UniProt
site_idPS60001
Number of Residues8
DetailsNOS Nitric oxide synthase (NOS) signature. RCVGRIqW
ChainResidueDetails
AARG183-TRP190

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:10074942, ECO:0000269|PubMed:12437348, ECO:0000269|PubMed:18849972, ECO:0000269|PubMed:25286850, ECO:0007744|PDB:1M9J, ECO:0007744|PDB:1M9K, ECO:0007744|PDB:1M9M, ECO:0007744|PDB:1M9Q, ECO:0007744|PDB:1M9R, ECO:0007744|PDB:3EAH, ECO:0007744|PDB:3NOS, ECO:0007744|PDB:4D1O, ECO:0007744|PDB:4D1P
ChainResidueDetails
ACYS94
ACYS99
BCYS94
BCYS99
CCYS94
CCYS99
DCYS94
DCYS99

site_idSWS_FT_FI2
Number of Residues40
DetailsBINDING: BINDING => ECO:0000269|PubMed:25286850, ECO:0007744|PDB:4D1O
ChainResidueDetails
AGLU361
AASN366
AALA446
ATRP447
APHE460
ATYR475
BSER102
BGLN247
BTRP356
BTYR357
BGLU361
BASN366
BALA446
BTRP447
BPHE460
BTYR475
CSER102
CGLN247
CTRP356
CTYR357
CGLU361
CASN366
CALA446
CTRP447
CPHE460
CTYR475
DSER102
DGLN247
DTRP356
DTYR357
DGLU361
DASN366
DALA446
DTRP447
DPHE460
DTYR475
ASER102
AGLN247
ATRP356
ATYR357

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: axial binding residue => ECO:0000269|PubMed:25286850, ECO:0007744|PDB:4D1O
ChainResidueDetails
ACYS184
BCYS184
CCYS184
DCYS184

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10074942, ECO:0000269|PubMed:25286850, ECO:0007744|PDB:3NOS, ECO:0007744|PDB:4D1O, ECO:0007744|PDB:4D1P
ChainResidueDetails
AARG365
CARG365
DARG365
BARG365

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: Phosphoserine; by CDK5 => ECO:0000269|PubMed:20213743
ChainResidueDetails
ASER114
BSER114
CSER114
DSER114

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 935
ChainResidueDetails
ACYS184metal ligand
AARG187steric role
ATRP356electrostatic stabiliser
AGLU361electrostatic stabiliser

site_idMCSA2
Number of Residues4
DetailsM-CSA 935
ChainResidueDetails
BCYS184metal ligand
BARG187steric role
BTRP356electrostatic stabiliser
BGLU361electrostatic stabiliser

site_idMCSA3
Number of Residues4
DetailsM-CSA 935
ChainResidueDetails
CCYS184metal ligand
CARG187steric role
CTRP356electrostatic stabiliser
CGLU361electrostatic stabiliser

site_idMCSA4
Number of Residues4
DetailsM-CSA 935
ChainResidueDetails
DCYS184metal ligand
DARG187steric role
DTRP356electrostatic stabiliser
DGLU361electrostatic stabiliser

221051

PDB entries from 2024-06-12

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