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6NH1

Structure of human endothelial nitric oxide synthase heme domain in complex with 6-(3-fluoro-5-(3-(methylamino)prop-1-yn-1-yl)phenethyl)-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 Residues16
Detailsbinding site for residue HEM A 501
ChainResidue
ATRP178
AMET358
AGLU361
ATRP447
APHE473
ATYR475
AKLY502
BH4B501
AARG183
ACYS184
AVAL185
ASER226
AMET339
APHE353
ASER354
ATRP356

site_idAC2
Number of Residues8
Detailsbinding site for residue KLY A 502
ChainResidue
AGLN247
AVAL336
AGLY355
ATRP356
ATYR357
AGLU361
AHEM501
BH4B501

site_idAC3
Number of Residues4
Detailsbinding site for residue BTB A 503
ChainResidue
AASP384
AGD509
DCYS382
DHOH621

site_idAC4
Number of Residues3
Detailsbinding site for residue BTB A 504
ChainResidue
AGLU377
ATHR387
DASP384

site_idAC5
Number of Residues1
Detailsbinding site for residue BTB A 505
ChainResidue
AGLU298

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

site_idAC7
Number of Residues1
Detailsbinding site for residue GOL A 507
ChainResidue
AGLU167

site_idAC8
Number of Residues3
Detailsbinding site for residue CL A 508
ChainResidue
AGLN247
ATYR357
AASN366

site_idAC9
Number of Residues1
Detailsbinding site for residue GD A 509
ChainResidue
ABTB503

site_idAD1
Number of Residues6
Detailsbinding site for residue BTB A 510
ChainResidue
AASP384
ALEU385
AARG388
CGLN257
DVAL381
DASP384

site_idAD2
Number of Residues10
Detailsbinding site for residue H4B B 501
ChainResidue
ASER102
AARG365
AALA446
AHEM501
AKLY502
BTRP445
BPHE460
BHIS461
BGLN462
BGLU463

site_idAD3
Number of Residues13
Detailsbinding site for residue HEM B 502
ChainResidue
BTRP178
BARG183
BCYS184
BPHE353
BSER354
BGLY355
BTRP356
BGLU361
BARG365
BTRP447
BTYR475
BH4B503
BKLY504

site_idAD4
Number of Residues9
Detailsbinding site for residue H4B B 503
ChainResidue
ATRP74
APHE460
AHIS461
BSER102
BALA446
BTRP447
BHEM502
BKLY504
BHOH611

site_idAD5
Number of Residues8
Detailsbinding site for residue KLY B 504
ChainResidue
BPRO334
BVAL336
BGLY355
BTRP356
BGLU361
BARG365
BHEM502
BH4B503

site_idAD6
Number of Residues9
Detailsbinding site for residue BTB B 505
ChainResidue
BTHR319
BGLU321
BGD508
BHOH609
BHOH612
CVAL261
CTYR373
CASN374
CASP378

site_idAD7
Number of Residues3
Detailsbinding site for residue BTB B 506
ChainResidue
BGLU298
BHOH607
DGLU167

site_idAD8
Number of Residues6
Detailsbinding site for residue CL B 507
ChainResidue
BGLN247
BARG250
BTYR357
BARG365
BASN366
BHOH640

site_idAD9
Number of Residues5
Detailsbinding site for residue GD B 508
ChainResidue
BTHR319
BGLU321
BBTB505
BHOH609
BHOH612

site_idAE1
Number of Residues4
Detailsbinding site for residue ZN B 509
ChainResidue
AHIS461
BASP369
BHOH611
BHOH635

site_idAE2
Number of Residues5
Detailsbinding site for residue BTB B 510
ChainResidue
BLEU326
BCYS382
CCYS382
CASP384
CGD508

site_idAE3
Number of Residues2
Detailsbinding site for residue BTB B 511
ChainResidue
BASP384
CGLU377

site_idAE4
Number of Residues8
Detailsbinding site for residue KLY C 503
ChainResidue
CVAL336
CPHE353
CGLY355
CTRP356
CTYR357
CGLU361
CHEM501
CH4B502

site_idAE5
Number of Residues1
Detailsbinding site for residue BTB C 504
ChainResidue
CGLU298

site_idAE6
Number of Residues4
Detailsbinding site for residue ZN C 505
ChainResidue
CCYS94
CCYS99
DCYS94
DCYS99

site_idAE7
Number of Residues2
Detailsbinding site for residue GOL C 506
ChainResidue
CGLU167
CHOH613

site_idAE8
Number of Residues3
Detailsbinding site for residue CL C 507
ChainResidue
CGLN247
CTYR357
CASN366

site_idAE9
Number of Residues1
Detailsbinding site for residue GD C 508
ChainResidue
BBTB510

site_idAF1
Number of Residues17
Detailsbinding site for residue HEM D 501
ChainResidue
DTRP178
DARG183
DCYS184
DVAL185
DPHE353
DSER354
DGLY355
DTRP356
DMET358
DGLU361
DARG365
DPHE473
DTYR475
DH4B502
DKLY503
DHOH611
DHOH637

site_idAF2
Number of Residues12
Detailsbinding site for residue H4B D 502
ChainResidue
CTRP74
CTRP445
CPHE460
CHIS461
DSER102
DVAL104
DALA446
DTRP447
DHEM501
DKLY503
DHOH603
DHOH639

site_idAF3
Number of Residues8
Detailsbinding site for residue KLY D 503
ChainResidue
DVAL336
DPHE353
DTRP356
DGLU361
DHEM501
DH4B502
DHOH603
DHOH611

site_idAF4
Number of Residues10
Detailsbinding site for residue BTB D 504
ChainResidue
AVAL261
AARG285
ATYR373
AASN374
AASP378
AHOH601
DTHR319
DGLU321
DGD506
DHOH606

site_idAF5
Number of Residues2
Detailsbinding site for residue BTB D 505
ChainResidue
DGLU298
DHOH633

site_idAF6
Number of Residues5
Detailsbinding site for residue GD D 506
ChainResidue
AHOH601
DTHR319
DGLU321
DBTB504
DHOH606

site_idAF7
Number of Residues5
Detailsbinding site for residue CL D 507
ChainResidue
DGLN247
DARG250
DTYR357
DARG365
DASN366

site_idAF8
Number of Residues4
Detailsbinding site for residue ZN D 508
ChainResidue
CHIS461
DASP369
DHOH639
DHOH641

site_idAF9
Number of Residues19
Detailsbinding site for residues HEM C 501 and H4B C 502
ChainResidue
CSER102
CTRP178
CARG183
CCYS184
CVAL185
CPHE353
CSER354
CTRP356
CMET358
CGLU361
CARG365
CALA446
CTRP447
CTYR475
CKLY503
CHOH610
DPHE460
DHIS461
DGLU463

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 2024-04-24

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