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3THR

Crystal structure of rat native liver Glycine N-methyltransferase complexed with 5-methyltetrahydrofolate monoglutamate

Functional Information from GO Data
ChainGOidnamespacecontents
A0005542molecular_functionfolic acid binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0005977biological_processglycogen metabolic process
A0006111biological_processregulation of gluconeogenesis
A0006544biological_processglycine metabolic process
A0006555biological_processmethionine metabolic process
A0006730biological_processone-carbon metabolic process
A0008168molecular_functionmethyltransferase activity
A0008757molecular_functionS-adenosylmethionine-dependent methyltransferase activity
A0016594molecular_functionglycine binding
A0017174molecular_functionglycine N-methyltransferase activity
A0032259biological_processmethylation
A0034708cellular_componentmethyltransferase complex
A0042802molecular_functionidentical protein binding
A0046498biological_processS-adenosylhomocysteine metabolic process
A0046500biological_processS-adenosylmethionine metabolic process
A0051289biological_processprotein homotetramerization
A0098603molecular_functionselenol Se-methyltransferase activity
A1901052biological_processsarcosine metabolic process
A1904047molecular_functionS-adenosyl-L-methionine binding
B0005542molecular_functionfolic acid binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0005977biological_processglycogen metabolic process
B0006111biological_processregulation of gluconeogenesis
B0006544biological_processglycine metabolic process
B0006555biological_processmethionine metabolic process
B0006730biological_processone-carbon metabolic process
B0008168molecular_functionmethyltransferase activity
B0008757molecular_functionS-adenosylmethionine-dependent methyltransferase activity
B0016594molecular_functionglycine binding
B0017174molecular_functionglycine N-methyltransferase activity
B0032259biological_processmethylation
B0034708cellular_componentmethyltransferase complex
B0042802molecular_functionidentical protein binding
B0046498biological_processS-adenosylhomocysteine metabolic process
B0046500biological_processS-adenosylmethionine metabolic process
B0051289biological_processprotein homotetramerization
B0098603molecular_functionselenol Se-methyltransferase activity
B1901052biological_processsarcosine metabolic process
B1904047molecular_functionS-adenosyl-L-methionine binding
C0005542molecular_functionfolic acid binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0005977biological_processglycogen metabolic process
C0006111biological_processregulation of gluconeogenesis
C0006544biological_processglycine metabolic process
C0006555biological_processmethionine metabolic process
C0006730biological_processone-carbon metabolic process
C0008168molecular_functionmethyltransferase activity
C0008757molecular_functionS-adenosylmethionine-dependent methyltransferase activity
C0016594molecular_functionglycine binding
C0017174molecular_functionglycine N-methyltransferase activity
C0032259biological_processmethylation
C0034708cellular_componentmethyltransferase complex
C0042802molecular_functionidentical protein binding
C0046498biological_processS-adenosylhomocysteine metabolic process
C0046500biological_processS-adenosylmethionine metabolic process
C0051289biological_processprotein homotetramerization
C0098603molecular_functionselenol Se-methyltransferase activity
C1901052biological_processsarcosine metabolic process
C1904047molecular_functionS-adenosyl-L-methionine binding
D0005542molecular_functionfolic acid binding
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0005977biological_processglycogen metabolic process
D0006111biological_processregulation of gluconeogenesis
D0006544biological_processglycine metabolic process
D0006555biological_processmethionine metabolic process
D0006730biological_processone-carbon metabolic process
D0008168molecular_functionmethyltransferase activity
D0008757molecular_functionS-adenosylmethionine-dependent methyltransferase activity
D0016594molecular_functionglycine binding
D0017174molecular_functionglycine N-methyltransferase activity
D0032259biological_processmethylation
D0034708cellular_componentmethyltransferase complex
D0042802molecular_functionidentical protein binding
D0046498biological_processS-adenosylhomocysteine metabolic process
D0046500biological_processS-adenosylmethionine metabolic process
D0051289biological_processprotein homotetramerization
D0098603molecular_functionselenol Se-methyltransferase activity
D1901052biological_processsarcosine metabolic process
D1904047molecular_functionS-adenosyl-L-methionine binding
Functional Information from PDB Data
site_idAC1
Number of Residues16
DetailsBINDING SITE FOR RESIDUE C2F A 1100
ChainResidue
ATYR5
BARG239
CSER3
CVAL4
CTYR5
DLEU207
DHIS214
DMET215
ATHR7
AHOH642
AHOH653
AHOH670
AHOH698
BLEU207
BHIS214
BTHR217

site_idAC2
Number of Residues12
DetailsBINDING SITE FOR RESIDUE TAM A 1500
ChainResidue
ATRP30
ATYR33
AILE34
ATHR37
AGLY137
ASER139
AHIS142
AHOH416
AHOH487
AHOH671
BALA13
BGLU15

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE C2F B 1700
ChainResidue
BTYR279
BVAL280
BCYS282

site_idAC4
Number of Residues9
DetailsBINDING SITE FOR RESIDUE C2F C 1410
ChainResidue
CARG59
CPRO125
CALA126
CHOH316
CHOH405
CHOH427
CHOH585
CHOH635
CHOH648

site_idAC5
Number of Residues13
DetailsBINDING SITE FOR RESIDUE TAM C 1600
ChainResidue
CTRP30
CTYR33
CILE34
CTHR37
CMET90
CGLY137
CHOH337
CHOH437
CHOH519
CHOH639
DALA13
DGLU15
DHOH387

site_idAC6
Number of Residues16
DetailsBINDING SITE FOR RESIDUE C2F D 1200
ChainResidue
ALEU207
AHIS214
AMET215
BSER3
BVAL4
BTYR5
CLEU207
CHIS214
CMET215
CTHR217
CARG239
CHOH317
DTYR5
DTHR7
DHOH369
DHOH627

site_idAC7
Number of Residues11
DetailsBINDING SITE FOR RESIDUE TAM D 1400
ChainResidue
CGLU15
DTYR33
DILE34
DMET90
DGLY137
DASN191
DHOH345
DHOH382
DHOH402
DHOH444
DHOH522

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:22037183, ECO:0000312|PDB:3THR, ECO:0000312|PDB:3THS
ChainResidueDetails
BHIS214
BARG239
CSER3
CHIS214
CARG239
DSER3
DHIS214
DARG239
AARG239
BSER3
ASER3
AHIS214

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:22037183, ECO:0000312|PDB:3THS
ChainResidueDetails
CTYR5
DTYR5
ATYR5
BTYR5

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12859184, ECO:0007744|PDB:1NBH
ChainResidueDetails
CTYR21
DTYR21
ATYR21
BTYR21

site_idSWS_FT_FI4
Number of Residues16
DetailsBINDING: BINDING => ECO:0000269|PubMed:12859184, ECO:0007744|PDB:1NBH, ECO:0007744|PDB:1NBI
ChainResidueDetails
CTRP30
CARG40
CASP85
CASN116
DTRP30
DARG40
DASP85
DASN116
AASN116
BTRP30
BARG40
BASP85
BASN116
ATRP30
AARG40
AASP85

site_idSWS_FT_FI5
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:8810903, ECO:0007744|PDB:1XVA
ChainResidueDetails
BARG175
BTYR220
CTYR33
CARG175
CTYR220
DTYR33
DARG175
DTYR220
BTYR33
ATYR33
AARG175
ATYR220

site_idSWS_FT_FI6
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12859184, ECO:0000269|PubMed:8810903, ECO:0000312|PDB:1XVA, ECO:0007744|PDB:1NBH, ECO:0007744|PDB:1NBI
ChainResidueDetails
BALA64
CALA64
DALA64
AALA64

site_idSWS_FT_FI7
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12859184, ECO:0000269|PubMed:8810903, ECO:0007744|PDB:1NBI, ECO:0007744|PDB:1XVA
ChainResidueDetails
CLEU136
DLEU136
ALEU136
BLEU136

site_idSWS_FT_FI8
Number of Residues4
DetailsMOD_RES: N-acetylvaline => ECO:0000269|PubMed:2822402
ChainResidueDetails
AVAL1
BVAL1
CVAL1
DVAL1

site_idSWS_FT_FI9
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:Q9QXF8
ChainResidueDetails
ASER9
BSER9
CSER9
DSER9

site_idSWS_FT_FI10
Number of Residues4
DetailsMOD_RES: Phosphotyrosine => ECO:0000250|UniProtKB:Q9QXF8
ChainResidueDetails
ATYR33
BTYR33
CTYR33
DTYR33

site_idSWS_FT_FI11
Number of Residues16
DetailsMOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:Q9QXF8
ChainResidueDetails
ALYS45
ALYS190
ALYS195
ALYS200
BLYS45
BLYS190
BLYS195
BLYS200
CLYS45
CLYS190
CLYS195
CLYS200
DLYS45
DLYS190
DLYS195
DLYS200

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 23
ChainResidueDetails
ATYR21electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
AGLY137electrostatic stabiliser, hydrogen bond acceptor
AHIS142activator
AARG175electrostatic stabiliser
ATYR194electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor

site_idMCSA2
Number of Residues5
DetailsM-CSA 23
ChainResidueDetails
BTYR21electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
BGLY137electrostatic stabiliser, hydrogen bond acceptor
BHIS142activator
BARG175electrostatic stabiliser
BTYR194electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor

site_idMCSA3
Number of Residues5
DetailsM-CSA 23
ChainResidueDetails
CTYR21electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
CGLY137electrostatic stabiliser, hydrogen bond acceptor
CHIS142activator
CARG175electrostatic stabiliser
CTYR194electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor

site_idMCSA4
Number of Residues5
DetailsM-CSA 23
ChainResidueDetails
DTYR21electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
DGLY137electrostatic stabiliser, hydrogen bond acceptor
DHIS142activator
DARG175electrostatic stabiliser
DTYR194electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor

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PDB entries from 2024-06-12

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