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6FW0

Crystal structure of human monoamine oxidase B (MAO B) in complex with chlorophenyl-chromone-carboxamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0005515molecular_functionprotein binding
A0005739cellular_componentmitochondrion
A0005740cellular_componentmitochondrial envelope
A0005741cellular_componentmitochondrial outer membrane
A0008131molecular_functionprimary amine oxidase activity
A0009055molecular_functionelectron transfer activity
A0009410biological_processresponse to xenobiotic stimulus
A0009636biological_processresponse to toxic substance
A0010044biological_processresponse to aluminum ion
A0010269biological_processresponse to selenium ion
A0014063biological_processnegative regulation of serotonin secretion
A0016491molecular_functionoxidoreductase activity
A0019607biological_processphenylethylamine catabolic process
A0021762biological_processsubstantia nigra development
A0030425cellular_componentdendrite
A0032496biological_processresponse to lipopolysaccharide
A0042420biological_processdopamine catabolic process
A0042802molecular_functionidentical protein binding
A0043025cellular_componentneuronal cell body
A0045471biological_processresponse to ethanol
A0045964biological_processpositive regulation of dopamine metabolic process
A0048545biological_processresponse to steroid hormone
A0050660molecular_functionflavin adenine dinucleotide binding
A0050665biological_processhydrogen peroxide biosynthetic process
A0051412biological_processresponse to corticosterone
A0052595molecular_functionaliphatic amine oxidase activity
A0097621molecular_functionmonoamine oxidase activity
B0005515molecular_functionprotein binding
B0005739cellular_componentmitochondrion
B0005740cellular_componentmitochondrial envelope
B0005741cellular_componentmitochondrial outer membrane
B0008131molecular_functionprimary amine oxidase activity
B0009055molecular_functionelectron transfer activity
B0009410biological_processresponse to xenobiotic stimulus
B0009636biological_processresponse to toxic substance
B0010044biological_processresponse to aluminum ion
B0010269biological_processresponse to selenium ion
B0014063biological_processnegative regulation of serotonin secretion
B0016491molecular_functionoxidoreductase activity
B0019607biological_processphenylethylamine catabolic process
B0021762biological_processsubstantia nigra development
B0030425cellular_componentdendrite
B0032496biological_processresponse to lipopolysaccharide
B0042420biological_processdopamine catabolic process
B0042802molecular_functionidentical protein binding
B0043025cellular_componentneuronal cell body
B0045471biological_processresponse to ethanol
B0045964biological_processpositive regulation of dopamine metabolic process
B0048545biological_processresponse to steroid hormone
B0050660molecular_functionflavin adenine dinucleotide binding
B0050665biological_processhydrogen peroxide biosynthetic process
B0051412biological_processresponse to corticosterone
B0052595molecular_functionaliphatic amine oxidase activity
B0097621molecular_functionmonoamine oxidase activity
Functional Information from PDB Data
site_idAC1
Number of Residues37
Detailsbinding site for residue FAD A 601
ChainResidue
AGLY11
AGLY41
AARG42
ATHR43
AGLY58
ASER59
ATYR60
APRO234
AVAL235
AALA263
AILE264
AGLY13
ATRP388
ATYR393
ACYS397
ATYR398
AGLY425
ATHR426
AGLY434
ATYR435
AMET436
AALA439
AILE14
AHOH742
AHOH803
AHOH842
AHOH882
AHOH899
AHOH928
AHOH950
AHOH979
ASER15
ALEU33
AGLU34
AALA35
AARG36
AGLY40

site_idAC2
Number of Residues10
Detailsbinding site for residue E92 A 602
ChainResidue
ALEU164
APHE168
ALEU171
ACYS172
AILE199
AGLN206
AILE316
ATYR326
ATYR398
ATYR435

site_idAC3
Number of Residues5
Detailsbinding site for residue C15 A 603
ChainResidue
AASP153
ALYS154
ACYS156
ATRP157
AHOH720

site_idAC4
Number of Residues7
Detailsbinding site for residue GOL A 604
ChainResidue
AHIS91
AGLY94
ALYS370
AHOH709
AHOH724
AHOH804
AHOH1052

site_idAC5
Number of Residues9
Detailsbinding site for residue E92 B 602
ChainResidue
BPHE168
BLEU171
BCYS172
BILE199
BGLN206
BTYR326
BPHE343
BTYR398
BTYR435

site_idAC6
Number of Residues4
Detailsbinding site for residue C15 B 603
ChainResidue
BASP153
BLYS154
BCYS156
BHOH877

site_idAC7
Number of Residues9
Detailsbinding site for residue GOL B 604
ChainResidue
BHIS91
BGLY94
BALA322
BHOH717
BHOH721
BHOH727
BHOH869
BHOH902
BHOH1075

site_idAC8
Number of Residues43
Detailsbinding site for Di-peptide FAD B 601 and CYS B 397
ChainResidue
BVAL235
BALA263
BILE264
BGLY292
BSER293
BVAL294
BTRP388
BTYR393
BGLY396
BTYR398
BTHR399
BGLY425
BTHR426
BGLY434
BTYR435
BMET436
BALA439
BHOH765
BHOH782
BHOH792
BHOH827
BHOH866
BHOH870
BHOH936
BHOH1031
BVAL10
BGLY11
BGLY13
BILE14
BSER15
BLEU33
BGLU34
BALA35
BARG36
BGLY40
BGLY41
BARG42
BTHR43
BGLY58
BSER59
BTYR60
BTHR174
BPRO234

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues974
DetailsTOPO_DOM: Cytoplasmic
ChainResidueDetails
ASER2-VAL489
BSER2-VAL489

site_idSWS_FT_FI2
Number of Residues52
DetailsTRANSMEM: Helical; Anchor for type IV membrane protein
ChainResidueDetails
APRO490-LEU516
BPRO490-LEU516

site_idSWS_FT_FI3
Number of Residues6
DetailsTOPO_DOM: Mitochondrial intermembrane
ChainResidueDetails
ALEU517-VAL520
BLEU517-VAL520

site_idSWS_FT_FI4
Number of Residues6
DetailsSITE: Important for catalytic activity
ChainResidueDetails
ACYS156
ACYS365
AHIS382
BCYS156
BCYS365
BHIS382

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: N-acetylserine => ECO:0000269|PubMed:11049757
ChainResidueDetails
ASER2
BSER2

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:Q8BW75
ChainResidueDetails
ALYS52
BLYS52

site_idSWS_FT_FI7
Number of Residues2
DetailsMOD_RES: S-8alpha-FAD cysteine => ECO:0000269|PubMed:11753429, ECO:0000269|PubMed:12913124, ECO:0000269|PubMed:15027868, ECO:0000269|PubMed:15710600, ECO:0000269|PubMed:16366596, ECO:0007744|PDB:1GOS, ECO:0007744|PDB:1OJ9, ECO:0007744|PDB:1OJA, ECO:0007744|PDB:1OJC, ECO:0007744|PDB:1OJD, ECO:0007744|PDB:1S2Q, ECO:0007744|PDB:1S2Y, ECO:0007744|PDB:1S3B, ECO:0007744|PDB:1S3E, ECO:0007744|PDB:2BK3, ECO:0007744|PDB:2BK4, ECO:0007744|PDB:2BK5, ECO:0007744|PDB:2BYB, ECO:0007744|PDB:2C64, ECO:0007744|PDB:2C65, ECO:0007744|PDB:2C66, ECO:0007744|PDB:2C67, ECO:0007744|PDB:2C70, ECO:0007744|PDB:2C72, ECO:0007744|PDB:2C73, ECO:0007744|PDB:2C75, ECO:0007744|PDB:2C76, ECO:0007744|PDB:2V5Z, ECO:0007744|PDB:2V60, ECO:0007744|PDB:2V61, ECO:0007744|PDB:2VRL, ECO:0007744|PDB:2VRM, ECO:0007744|PDB:2VZ2, ECO:0007744|PDB:2XFN, ECO:0007744|PDB:2XFO, ECO:0007744|PDB:2XFP, ECO:0007744|PDB:2XFQ, ECO:0007744|PDB:3PO7, ECO:0007744|PDB:3ZYX, ECO:0007744|PDB:4A79, ECO:0007744|PDB:4A7A, ECO:0007744|PDB:4CRT, ECO:0007744|PDB:5MRL
ChainResidueDetails
ACYS397
BCYS397

221051

PDB entries from 2024-06-12

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