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5VVC

Structure of human endothelial nitric oxide synthase heme domain in complex with 4-(2-(((2-Amino-4-methylquinolin-7-yl)methyl)amino)ethyl)-2-methylbenzonitrile

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 Residues14
Detailsbinding site for residue HEM A 501
ChainResidue
ATRP178
APHE473
ATYR475
AH4B502
A9OJ503
AHOH641
ACYS184
ASER226
APHE353
ASER354
AGLY355
ATRP356
AGLU361
ATRP447

site_idAC2
Number of Residues12
Detailsbinding site for residue H4B A 502
ChainResidue
ASER102
AARG365
AALA446
ATRP447
AHEM501
AHOH617
AHOH631
BTRP445
BPHE460
BHIS461
BGLN462
BGLU463

site_idAC3
Number of Residues9
Detailsbinding site for residue 9OJ A 503
ChainResidue
APHE105
AVAL336
APHE353
ATRP356
ATYR357
AGLU361
ATYR475
AHEM501
BTRP74

site_idAC4
Number of Residues11
Detailsbinding site for residue BTB A 504
ChainResidue
ATRP322
ACYS382
AASP384
AGD510
AHOH610
AHOH615
AHOH643
DTRP322
DALA325
DLEU326
DASP378

site_idAC5
Number of Residues4
Detailsbinding site for residue BTB A 505
ChainResidue
AGLU377
ATHR387
AHOH602
DASP384

site_idAC6
Number of Residues1
Detailsbinding site for residue BTB A 506
ChainResidue
AGLU298

site_idAC7
Number of Residues4
Detailsbinding site for residue ZN A 507
ChainResidue
ACYS94
ACYS99
BCYS94
BCYS99

site_idAC8
Number of Residues2
Detailsbinding site for residue GOL A 508
ChainResidue
AGLU167
AHOH634

site_idAC9
Number of Residues2
Detailsbinding site for residue CL A 509
ChainResidue
ATYR357
AASN366

site_idAD1
Number of Residues4
Detailsbinding site for residue GD A 510
ChainResidue
ABTB504
AHOH615
AHOH643
AHOH674

site_idAD2
Number of Residues16
Detailsbinding site for residue HEM B 501
ChainResidue
BTRP178
BALA181
BARG183
BCYS184
BSER226
BPHE353
BSER354
BTRP356
BGLU361
BTRP447
BPHE473
BTYR475
BH4B502
B9OJ503
BHOH633
BHOH660

site_idAD3
Number of Residues10
Detailsbinding site for residue H4B B 502
ChainResidue
ATRP445
APHE460
AGLU463
AHOH646
BSER102
BARG365
BALA446
BTRP447
BHEM501
BHOH640

site_idAD4
Number of Residues10
Detailsbinding site for residue 9OJ B 503
ChainResidue
ATRP74
BPHE105
BVAL336
BPHE353
BTRP356
BTYR357
BGLU361
BTRP447
BTYR475
BHEM501

site_idAD5
Number of Residues8
Detailsbinding site for residue BTB B 504
ChainResidue
BTHR319
BGLU321
BGD507
BHOH664
CVAL261
CTYR373
CASP378
CHOH602

site_idAD6
Number of Residues10
Detailsbinding site for residue BTB B 505
ChainResidue
BASP297
BGLU298
BHOH606
BHOH614
BHOH616
BHOH629
BHOH655
BHOH673
BHOH686
DGLU167

site_idAD7
Number of Residues6
Detailsbinding site for residue CL B 506
ChainResidue
BGLN247
BARG250
BTYR357
BASN366
BHOH620
BHOH659

site_idAD8
Number of Residues5
Detailsbinding site for residue GD B 507
ChainResidue
BTHR319
BGLU321
BBTB504
BHOH664
CHOH602

site_idAD9
Number of Residues8
Detailsbinding site for residue BTB B 508
ChainResidue
BTRP322
BALA325
BLEU326
BASP378
CVAL381
CCYS382
CASP384
CGD510

site_idAE1
Number of Residues15
Detailsbinding site for residue HEM C 501
ChainResidue
CTRP178
CALA181
CCYS184
CSER226
CPHE353
CSER354
CGLY355
CTRP356
CMET358
CGLU361
CPHE473
CTYR475
CH4B502
C9OJ503
CHOH623

site_idAE2
Number of Residues10
Detailsbinding site for residue H4B C 502
ChainResidue
CSER102
CARG365
CALA446
CTRP447
CHEM501
CHOH623
CHOH630
CHOH646
DTRP445
DPHE460

site_idAE3
Number of Residues8
Detailsbinding site for residue 9OJ C 503
ChainResidue
CPHE105
CVAL336
CTRP356
CGLU361
CTRP447
CTYR475
CHEM501
DTRP74

site_idAE4
Number of Residues7
Detailsbinding site for residue BTB C 504
ChainResidue
BMET383
BASP384
CGLU377
CARG388
CHOH606
CHOH609
CHOH655

site_idAE5
Number of Residues3
Detailsbinding site for residue BTB C 505
ChainResidue
CGLU298
CHOH601
CHOH612

site_idAE6
Number of Residues7
Detailsbinding site for residue BTB C 506
ChainResidue
CGLN90
CGLN122
CGLN126
CGLU342
CGLY345
CGLU347
CARG474

site_idAE7
Number of Residues4
Detailsbinding site for residue ZN C 507
ChainResidue
CCYS94
CCYS99
DCYS94
DCYS99

site_idAE8
Number of Residues2
Detailsbinding site for residue GOL C 508
ChainResidue
CGLU167
CHOH651

site_idAE9
Number of Residues4
Detailsbinding site for residue CL C 509
ChainResidue
CGLN247
CTYR357
CASN366
CHOH658

site_idAF1
Number of Residues1
Detailsbinding site for residue GD C 510
ChainResidue
BBTB508

site_idAF2
Number of Residues16
Detailsbinding site for residue HEM D 501
ChainResidue
DTRP178
DALA181
DARG183
DCYS184
DSER226
DPHE353
DSER354
DTRP356
DMET358
DGLU361
DTRP447
DPHE473
DTYR475
DH4B502
D9OJ503
DHOH609

site_idAF3
Number of Residues9
Detailsbinding site for residue H4B D 502
ChainResidue
CTRP445
CPHE460
DSER102
DARG365
DALA446
DTRP447
DHEM501
DHOH609
DHOH680

site_idAF4
Number of Residues9
Detailsbinding site for residue 9OJ D 503
ChainResidue
CTRP74
DVAL104
DPHE105
DVAL336
DPHE353
DTRP356
DGLU361
DTRP447
DHEM501

site_idAF5
Number of Residues8
Detailsbinding site for residue BTB D 504
ChainResidue
ASER260
ATYR373
AASN374
AASP378
DTHR319
DGLU321
DGD506
DHOH616

site_idAF6
Number of Residues7
Detailsbinding site for residue BTB D 505
ChainResidue
DASP297
DGLU298
DHOH614
DHOH624
DHOH632
DHOH644
DHOH652

site_idAF7
Number of Residues5
Detailsbinding site for residue GD D 506
ChainResidue
DTHR319
DGLU321
DBTB504
DHOH606
DHOH616

site_idAF8
Number of Residues6
Detailsbinding site for residue CL D 507
ChainResidue
DGLN247
DARG250
DTYR357
DASN366
DHOH669
DHOH698

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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