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6POW

Structure of human endotheial nitric oxide synthase heme domain in complex with 7-(5-(Aminomethyl)pyridin-3-yl)-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
AH4B502
AOUA503
AHOH644
AALA181
ACYS184
APHE353
ASER354
ATRP356
AGLU361
APHE473
ATYR475

site_idAC2
Number of Residues11
Detailsbinding site for residue H4B A 502
ChainResidue
ASER102
AVAL104
AARG365
AALA446
ATRP447
AHEM501
AOUA503
AHOH665
BPHE460
BGLN462
BGLU463

site_idAC3
Number of Residues7
Detailsbinding site for residue OUA A 503
ChainResidue
AVAL336
APHE353
ATRP356
ATYR357
AGLU361
AHEM501
AH4B502

site_idAC4
Number of Residues11
Detailsbinding site for residue BTB A 504
ChainResidue
AVAL381
AASP384
ALEU385
AARG388
AHOH601
AHOH640
CGLN257
CGD501
DVAL381
DCYS382
DASP384

site_idAC5
Number of Residues2
Detailsbinding site for residue BTB A 505
ChainResidue
ATHR387
DASP384

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

site_idAC7
Number of Residues4
Detailsbinding site for residue GOL A 507
ChainResidue
AGLU167
AHOH605
AHOH624
AHOH674

site_idAC8
Number of Residues2
Detailsbinding site for residue CL A 508
ChainResidue
ATYR357
AASN366

site_idAC9
Number of Residues14
Detailsbinding site for residue HEM B 501
ChainResidue
BTRP178
BARG183
BCYS184
BSER226
BPHE353
BSER354
BTRP356
BMET358
BGLU361
BPHE473
BTYR475
BOUA502
BHOH732
BHOH735

site_idAD1
Number of Residues6
Detailsbinding site for residue OUA B 502
ChainResidue
BVAL336
BTRP356
BTYR357
BGLU361
BHEM501
BHOH602

site_idAD2
Number of Residues11
Detailsbinding site for residue OUA B 503
ChainResidue
ATRP74
ATRP445
APHE460
BSER102
BVAL104
BARG365
BASP369
BHIS371
BALA446
BTRP447
BHOH735

site_idAD3
Number of Residues8
Detailsbinding site for residue BTB B 504
ChainResidue
BTHR319
BGLU321
BGD507
BHOH607
BHOH610
CTYR373
CASN374
CASP378

site_idAD4
Number of Residues3
Detailsbinding site for residue BTB B 505
ChainResidue
BGLU298
BHOH627
DGLU167

site_idAD5
Number of Residues4
Detailsbinding site for residue CL B 506
ChainResidue
BGLN247
BTYR357
BASN366
BHOH659

site_idAD6
Number of Residues5
Detailsbinding site for residue GD B 507
ChainResidue
BTHR319
BGLU321
BBTB504
BHOH607
BHOH610

site_idAD7
Number of Residues4
Detailsbinding site for residue BTB B 508
ChainResidue
BASP384
BHOH619
CGLU377
CTHR387

site_idAD8
Number of Residues3
Detailsbinding site for residue GD C 501
ChainResidue
ABTB504
AHOH640
CGLN257

site_idAD9
Number of Residues15
Detailsbinding site for residue HEM C 502
ChainResidue
CTRP178
CARG183
CCYS184
CVAL185
CSER226
CMET339
CPHE353
CSER354
CGLY355
CTRP356
CGLU361
CTYR475
CH4B503
COUA504
CHOH615

site_idAE1
Number of Residues13
Detailsbinding site for residue H4B C 503
ChainResidue
CSER102
CVAL104
CARG365
CALA446
CTRP447
CHEM502
COUA504
CHOH644
CHOH682
DTRP445
DPHE460
DGLN462
DGLU463

site_idAE2
Number of Residues6
Detailsbinding site for residue OUA C 504
ChainResidue
CVAL336
CPHE353
CTRP356
CGLU361
CHEM502
CH4B503

site_idAE3
Number of Residues8
Detailsbinding site for residue BTB C 505
ChainResidue
BTRP322
BALA325
BLEU326
CTRP322
CVAL381
CCYS382
CASP384
CGD510

site_idAE4
Number of Residues3
Detailsbinding site for residue BTB C 506
ChainResidue
CGLU298
CHOH635
CHOH683

site_idAE5
Number of Residues4
Detailsbinding site for residue ZN C 507
ChainResidue
CCYS94
CCYS99
DCYS94
DCYS99

site_idAE6
Number of Residues1
Detailsbinding site for residue GOL C 508
ChainResidue
CGLU167

site_idAE7
Number of Residues3
Detailsbinding site for residue CL C 509
ChainResidue
CGLN247
CTYR357
CASN366

site_idAE8
Number of Residues4
Detailsbinding site for residue GD C 510
ChainResidue
CASP384
CBTB505
CHOH704
CHOH716

site_idAE9
Number of Residues16
Detailsbinding site for residue HEM D 501
ChainResidue
DTRP178
DCYS184
DSER226
DPHE353
DSER354
DGLY355
DTRP356
DMET358
DGLU361
DPHE473
DTYR475
DOUA502
DHOH628
DHOH653
DHOH655
DHOH741

site_idAF1
Number of Residues7
Detailsbinding site for residue OUA D 502
ChainResidue
DVAL336
DTRP356
DTYR357
DGLU361
DHEM501
DHOH692
DHOH722

site_idAF2
Number of Residues16
Detailsbinding site for residue OUA D 503
ChainResidue
CTRP74
CTRP445
CPHE460
CHOH618
DSER102
DVAL104
DARG365
DASP369
DHIS371
DALA446
DTRP447
DHOH610
DHOH628
DHOH655
DHOH683
DHOH692

site_idAF3
Number of Residues10
Detailsbinding site for residue BTB D 504
ChainResidue
ASER260
ATYR373
AASN374
AGLU377
AASP378
DTHR319
DGLU321
DGD506
DHOH630
DHOH736

site_idAF4
Number of Residues5
Detailsbinding site for residue BTB D 505
ChainResidue
DASP297
DGLU298
DPRO299
DHOH608
DHOH733

site_idAF5
Number of Residues5
Detailsbinding site for residue GD D 506
ChainResidue
AHOH602
DTHR319
DGLU321
DBTB504
DHOH630

site_idAF6
Number of Residues4
Detailsbinding site for residue CL D 507
ChainResidue
DGLN247
DTYR357
DASN366
DHOH680

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
ASER102
ATYR475
BSER102
BGLN247
BTRP356
BTYR357
BGLU361
BASN366
BALA446
BTRP447
BPHE460
AGLN247
BTYR475
CSER102
CGLN247
CTRP356
CTYR357
CGLU361
CASN366
CALA446
CTRP447
CPHE460
ATRP356
CTYR475
DSER102
DGLN247
DTRP356
DTYR357
DGLU361
DASN366
DALA446
DTRP447
DPHE460
ATYR357
DTYR475
AGLU361
AASN366
AALA446
ATRP447
APHE460

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
BARG365
CARG365
DARG365

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

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PDB entries from 2024-11-06

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