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4MIK

Crystal Structure of hPNMT in Complex with bisubstrate inhibitor (2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-(((2-(((7-nitro-1,2,3,4-tetrahydroisoquinolin-3-yl)methyl)amino)ethyl)thio)methyl)tetrahydrofuran-3,4-diol

Functional Information from GO Data
ChainGOidnamespacecontents
A0004603molecular_functionphenylethanolamine N-methyltransferase activity
A0005515molecular_functionprotein binding
A0005829cellular_componentcytosol
A0008168molecular_functionmethyltransferase activity
A0032259biological_processmethylation
A0042418biological_processepinephrine biosynthetic process
A0042423biological_processcatecholamine biosynthetic process
B0004603molecular_functionphenylethanolamine N-methyltransferase activity
B0005515molecular_functionprotein binding
B0005829cellular_componentcytosol
B0008168molecular_functionmethyltransferase activity
B0032259biological_processmethylation
B0042418biological_processepinephrine biosynthetic process
B0042423biological_processcatecholamine biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues27
DetailsBINDING SITE FOR RESIDUE JIL A 301
ChainResidue
ATYR27
AASN106
AASP158
AVAL159
AHIS160
APHE182
ACYS183
AALA186
AVAL187
AGLU219
ATYR222
ATYR35
AMET258
AASP267
ATRS302
AHOH402
AHOH479
AHOH504
AHOH521
AHOH544
AASN39
AVAL53
ALYS57
AGLY81
AASP101
APHE102
ALEU103

site_idAC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE TRS A 302
ChainResidue
ATYR35
ATYR40
AGLY79
ASER80
ATHR83
ATYR85
AALA181
APHE182
AJIL301
AHOH421

site_idAC3
Number of Residues25
DetailsBINDING SITE FOR RESIDUE JIL B 301
ChainResidue
BTYR27
BTYR35
BASN39
BTYR40
BLYS57
BGLY81
BASP101
BPHE102
BLEU103
BASN106
BASP158
BVAL159
BHIS160
BPHE182
BCYS183
BALA186
BVAL187
BGLU219
BTYR222
BASP267
BTRS302
BHOH429
BHOH510
BHOH537
BHOH552

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE TRS B 302
ChainResidue
BTYR35
BTYR40
BGLY79
BSER80
BGLY81
BTHR83
BTYR85
BALA181
BPHE182
BJIL301
BHOH404

Functional Information from PROSITE/UniProt
site_idPS01100
Number of Residues17
DetailsNNMT_PNMT_TEMT NNMT/PNMT/TEMT family of methyltransferases signature. LIDIGSGPTVYQLLSAC
ChainResidueDetails
ALEU75-CYS91

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:16363801, ECO:0000269|PubMed:17845018, ECO:0007744|PDB:2AN4, ECO:0007744|PDB:2G70, ECO:0007744|PDB:2G72
ChainResidueDetails
ATYR35
BASP101
BASN106
BALA181
ATYR40
ATYR85
AASP101
AASN106
AALA181
BTYR35
BTYR40
BTYR85

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:17845018, ECO:0007744|PDB:2G70, ECO:0007744|PDB:2G72
ChainResidueDetails
AGLY79
AASP158
BGLY79
BASP158

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:16363801, ECO:0007744|PDB:2AN4
ChainResidueDetails
AGLU219
AASP267
BGLU219
BASP267

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163
ChainResidueDetails
ASER7
BSER7

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PDB entries from 2024-07-10

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