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6NH8

Structure of human endothelial nitric oxide synthase heme domain in complex with 6-(5-(3-(dimethylamino)propyl)-2,3,4-trifluorophenethyl)-4-methylpyridin-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 Residues17
Detailsbinding site for residue HEM A 501
ChainResidue
ATRP178
AGLU361
ATRP447
ATYR475
AH4B502
AKMS503
AHOH620
AHOH621
AHOH643
AARG183
ACYS184
ASER226
APHE353
ASER354
AGLY355
ATRP356
AMET358

site_idAC2
Number of Residues12
Detailsbinding site for residue H4B A 502
ChainResidue
ASER102
AARG365
AALA446
ATRP447
AHEM501
AHOH613
AHOH621
BTRP445
BPHE460
BHIS461
BGLN462
BGLU463

site_idAC3
Number of Residues11
Detailsbinding site for residue KMS A 503
ChainResidue
APHE105
AGLN247
AVAL336
AASN338
APHE353
ATRP356
AGLU361
ATRP447
AHEM501
ACL509
AHOH621

site_idAC4
Number of Residues9
Detailsbinding site for residue BTB A 504
ChainResidue
ATRP322
AVAL381
ACYS382
AASP384
AGD510
AHOH645
DLEU326
DASP378
DCYS382

site_idAC5
Number of Residues4
Detailsbinding site for residue BTB A 505
ChainResidue
AGLU377
ATHR387
AARG388
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 Residues1
Detailsbinding site for residue GOL A 508
ChainResidue
AGLU167

site_idAC9
Number of Residues5
Detailsbinding site for residue CL A 509
ChainResidue
AGLN247
ATYR357
AASN366
AKMS503
AHOH630

site_idAD1
Number of Residues5
Detailsbinding site for residue GD A 510
ChainResidue
ABTB504
AHOH645
AHOH736
DHOH623
DHOH795

site_idAD2
Number of Residues17
Detailsbinding site for residue HEM B 501
ChainResidue
BTRP178
BARG183
BCYS184
BSER226
BPHE353
BSER354
BTRP356
BMET358
BGLU361
BTRP447
BPHE473
BTYR475
BH4B502
BKMS503
BHOH603
BHOH627
BHOH682

site_idAD3
Number of Residues12
Detailsbinding site for residue H4B B 502
ChainResidue
ATRP445
APHE460
AGLU463
AHOH648
BSER102
BARG365
BALA446
BTRP447
BHEM501
BHOH630
BHOH637
BHOH682

site_idAD4
Number of Residues14
Detailsbinding site for residue KMS B 503
ChainResidue
BVAL336
BASN338
BPHE353
BGLY355
BTRP356
BGLU361
BTRP447
BTYR475
BHEM501
BCL507
BHOH627
BHOH682
BHOH734
BGLN247

site_idAD5
Number of Residues9
Detailsbinding site for residue BTB B 504
ChainResidue
BTHR319
BGLU321
BGD508
BHOH736
CSER260
CVAL261
CASN374
CASP378
CHOH650

site_idAD6
Number of Residues3
Detailsbinding site for residue BTB B 505
ChainResidue
BGLU298
BHOH602
DGLU167

site_idAD7
Number of Residues1
Detailsbinding site for residue BTB B 506
ChainResidue
BGLU377

site_idAD8
Number of Residues5
Detailsbinding site for residue CL B 507
ChainResidue
BGLN247
BTYR357
BASN366
BKMS503
BHOH734

site_idAD9
Number of Residues5
Detailsbinding site for residue GD B 508
ChainResidue
BTHR319
BGLU321
BBTB504
BHOH736
CHOH607

site_idAE1
Number of Residues14
Detailsbinding site for residue HEM C 501
ChainResidue
CTRP178
CARG183
CCYS184
CSER226
CPHE353
CSER354
CTRP356
CMET358
CGLU361
CTRP447
CTYR475
CH4B502
CKMS503
CHOH641

site_idAE2
Number of Residues12
Detailsbinding site for residue H4B C 502
ChainResidue
CSER102
CVAL104
CARG365
CALA446
CTRP447
CHEM501
CHOH641
CHOH649
DTRP445
DPHE460
DGLU463
DHOH736

site_idAE3
Number of Residues12
Detailsbinding site for residue KMS C 503
ChainResidue
CPHE105
CGLN247
CPRO334
CVAL336
CPHE353
CTRP356
CGLU361
CTRP447
CHEM501
CCL509
CHOH641
CHOH723

site_idAE4
Number of Residues10
Detailsbinding site for residue BTB C 504
ChainResidue
BTRP322
BALA325
BLEU326
BCYS382
CVAL381
CCYS382
CASP384
CGD510
CHOH601
CHOH602

site_idAE5
Number of Residues3
Detailsbinding site for residue BTB C 505
ChainResidue
BASP384
CGLU377
CARG388

site_idAE6
Number of Residues1
Detailsbinding site for residue BTB C 506
ChainResidue
CGLU298

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

site_idAE8
Number of Residues1
Detailsbinding site for residue GOL C 508
ChainResidue
CGLU167

site_idAE9
Number of Residues4
Detailsbinding site for residue CL C 509
ChainResidue
CGLN247
CTYR357
CASN366
CKMS503

site_idAF1
Number of Residues3
Detailsbinding site for residue GD C 510
ChainResidue
CBTB504
CHOH601
CHOH741

site_idAF2
Number of Residues14
Detailsbinding site for residue HEM D 501
ChainResidue
DTRP178
DARG183
DCYS184
DSER226
DPHE353
DSER354
DTRP356
DGLU361
DPHE473
DTYR475
DH4B502
DKMS503
DHOH611
DHOH634

site_idAF3
Number of Residues11
Detailsbinding site for residue H4B D 502
ChainResidue
CTRP445
CPHE460
CGLU463
DSER102
DARG365
DALA446
DTRP447
DHEM501
DKMS503
DHOH611
DHOH637

site_idAF4
Number of Residues14
Detailsbinding site for residue KMS D 503
ChainResidue
DVAL104
DVAL336
DPHE353
DTRP356
DGLU361
DTRP447
DHEM501
DH4B502
DCL506
DHOH611
DHOH748
DHOH790
DHOH800
DHOH828

site_idAF5
Number of Residues7
Detailsbinding site for residue BTB D 504
ChainResidue
ASER260
ATYR373
AASN374
AASP378
DTHR319
DGLU321
DGD507

site_idAF6
Number of Residues2
Detailsbinding site for residue BTB D 505
ChainResidue
DGLU298
DHOH604

site_idAF7
Number of Residues5
Detailsbinding site for residue CL D 506
ChainResidue
DGLN247
DTYR357
DASN366
DKMS503
DHOH748

site_idAF8
Number of Residues5
Detailsbinding site for residue GD D 507
ChainResidue
AHOH606
DTHR319
DGLU321
DBTB504
DHOH783

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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