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7BSJ

Crystal structure of human ME2 R484W

Functional Information from GO Data
ChainGOidnamespacecontents
A0004470molecular_functionmalic enzyme activity
A0004471molecular_functionmalate dehydrogenase (decarboxylating) (NAD+) activity
A0004473molecular_functionmalate dehydrogenase (decarboxylating) (NADP+) activity
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
A0006090biological_processpyruvate metabolic process
A0006108biological_processmalate metabolic process
A0008948molecular_functionoxaloacetate decarboxylase activity
A0009055molecular_functionelectron transfer activity
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0043231cellular_componentintracellular membrane-bounded organelle
A0046872molecular_functionmetal ion binding
A0051287molecular_functionNAD binding
A1902031biological_processregulation of NADP metabolic process
B0004470molecular_functionmalic enzyme activity
B0004471molecular_functionmalate dehydrogenase (decarboxylating) (NAD+) activity
B0004473molecular_functionmalate dehydrogenase (decarboxylating) (NADP+) activity
B0005739cellular_componentmitochondrion
B0005759cellular_componentmitochondrial matrix
B0006090biological_processpyruvate metabolic process
B0006108biological_processmalate metabolic process
B0008948molecular_functionoxaloacetate decarboxylase activity
B0009055molecular_functionelectron transfer activity
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0043231cellular_componentintracellular membrane-bounded organelle
B0046872molecular_functionmetal ion binding
B0051287molecular_functionNAD binding
B1902031biological_processregulation of NADP metabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues26
Detailsbinding site for residue NAD A 601
ChainResidue
AARG165
AGLU314
AALA315
APHE344
AASP345
ALYS346
AVAL392
AALA393
AGLY394
AALA395
ALEU398
ALEU167
ALEU419
AASN421
AGLY446
AGLY465
AASN466
AASN467
ATTN605
AGLY168
AASN259
ATHR283
ALEU310
AGLY311
AALA312
AGLY313

site_idAC2
Number of Residues4
Detailsbinding site for residue MG A 602
ChainResidue
AGLU255
AASP256
AASP279
ATTN605

site_idAC3
Number of Residues13
Detailsbinding site for residue NAD A 603
ChainResidue
ALYS156
AGLY192
AILE193
AARG194
AARG197
AILE479
ALEU480
AASN482
AARG542
ATYR552
AGLU555
AARG556
BARG248

site_idAC4
Number of Residues11
Detailsbinding site for residue FUM A 604
ChainResidue
AGLN64
AARG67
AILE88
AARG91
ALEU95
AHOH701
AHOH702
AHOH703
AHOH705
BPHE127
BARG128

site_idAC5
Number of Residues12
Detailsbinding site for residue TTN A 605
ChainResidue
ATYR112
AARG165
ALEU167
ALYS183
AGLU255
AASP256
AASP279
AASN421
AASN466
AASN467
ANAD601
AMG602

site_idAC6
Number of Residues26
Detailsbinding site for residue NAD B 1601
ChainResidue
BARG165
BLEU167
BGLY168
BASN259
BTHR283
BLEU310
BGLY311
BALA312
BGLY313
BGLU314
BALA315
BASP345
BLYS346
BVAL392
BALA393
BGLY394
BALA395
BLEU398
BLEU419
BSER420
BASN421
BGLY446
BGLY465
BASN466
BASN467
BTTN1605

site_idAC7
Number of Residues5
Detailsbinding site for residue MG B 1602
ChainResidue
BARG165
BGLU255
BASP256
BASP279
BTTN1605

site_idAC8
Number of Residues17
Detailsbinding site for residue NAD B 1603
ChainResidue
AASP244
AARG245
ATYR246
AGLY247
BHIS154
BLYS156
BGLY192
BILE193
BARG194
BILE479
BLEU480
BASN482
BARG542
BTYR552
BARG556
AASN153
AHIS154

site_idAC9
Number of Residues6
Detailsbinding site for residue FUM B 1604
ChainResidue
APHE127
BGLN64
BARG67
BARG91
BLEU95
BHOH1705

site_idAD1
Number of Residues12
Detailsbinding site for residue TTN B 1605
ChainResidue
BTYR112
BARG165
BLEU167
BLYS183
BGLU255
BASP256
BASP279
BASN421
BASN466
BASN467
BNAD1601
BMG1602

Functional Information from PROSITE/UniProt
site_idPS00331
Number of Residues17
DetailsMALIC_ENZYMES Malic enzymes signature. FnDDiqGTAaVaLAGLL
ChainResidueDetails
APHE276-LEU292

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton donor => ECO:0000269|PubMed:12962632
ChainResidueDetails
ATYR112
BTYR112

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000269|PubMed:12962632
ChainResidueDetails
ALYS183
BLYS183

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12121650, ECO:0000269|PubMed:12962632
ChainResidueDetails
AARG67
AARG91
BARG67
BARG91

site_idSWS_FT_FI4
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:12962632
ChainResidueDetails
AARG165
AASN421
AASN466
BARG165
BASN421
BASN466

site_idSWS_FT_FI5
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:10700286, ECO:0000269|PubMed:12121650, ECO:0000269|PubMed:12962632
ChainResidueDetails
AGLU255
AASP256
AASP279
BGLU255
BASP256
BASP279

site_idSWS_FT_FI6
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10700286, ECO:0000269|PubMed:12962632
ChainResidueDetails
AASN259
AGLY311
BASN259
BGLY311

site_idSWS_FT_FI7
Number of Residues10
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS156
BLYS346
ALYS224
ALYS240
ALYS272
ALYS346
BLYS156
BLYS224
BLYS240
BLYS272

Catalytic Information from CSA
site_idMCSA1
Number of Residues8
DetailsM-CSA 21
ChainResidueDetails
ATYR112electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AARG165electrostatic stabiliser, hydrogen bond donor
ALYS183electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
AGLU255metal ligand
AASP256metal ligand
AASP278hydrogen bond acceptor, proton acceptor, proton donor
AASP279metal ligand
AASN421electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues8
DetailsM-CSA 21
ChainResidueDetails
BTYR112electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BARG165electrostatic stabiliser, hydrogen bond donor
BLYS183electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
BGLU255metal ligand
BASP256metal ligand
BASP278hydrogen bond acceptor, proton acceptor, proton donor
BASP279metal ligand
BASN421electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2024-07-10

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