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2NU8

C123aT Mutant of E. coli Succinyl-CoA Synthetase

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0003824molecular_functioncatalytic activity
A0004775molecular_functionsuccinate-CoA ligase (ADP-forming) activity
A0004776molecular_functionsuccinate-CoA ligase (GDP-forming) activity
A0005515molecular_functionprotein binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006099biological_processtricarboxylic acid cycle
A0009361cellular_componentsuccinate-CoA ligase complex (ADP-forming)
A0016874molecular_functionligase activity
B0000287molecular_functionmagnesium ion binding
B0003824molecular_functioncatalytic activity
B0004775molecular_functionsuccinate-CoA ligase (ADP-forming) activity
B0004776molecular_functionsuccinate-CoA ligase (GDP-forming) activity
B0005515molecular_functionprotein binding
B0005524molecular_functionATP binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006099biological_processtricarboxylic acid cycle
B0006104biological_processsuccinyl-CoA metabolic process
B0009361cellular_componentsuccinate-CoA ligase complex (ADP-forming)
B0016874molecular_functionligase activity
B0042709cellular_componentsuccinate-CoA ligase complex
B0046872molecular_functionmetal ion binding
D0000166molecular_functionnucleotide binding
D0003824molecular_functioncatalytic activity
D0004775molecular_functionsuccinate-CoA ligase (ADP-forming) activity
D0004776molecular_functionsuccinate-CoA ligase (GDP-forming) activity
D0005515molecular_functionprotein binding
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0006099biological_processtricarboxylic acid cycle
D0009361cellular_componentsuccinate-CoA ligase complex (ADP-forming)
D0016874molecular_functionligase activity
E0000287molecular_functionmagnesium ion binding
E0003824molecular_functioncatalytic activity
E0004775molecular_functionsuccinate-CoA ligase (ADP-forming) activity
E0004776molecular_functionsuccinate-CoA ligase (GDP-forming) activity
E0005515molecular_functionprotein binding
E0005524molecular_functionATP binding
E0005737cellular_componentcytoplasm
E0005829cellular_componentcytosol
E0006099biological_processtricarboxylic acid cycle
E0006104biological_processsuccinyl-CoA metabolic process
E0009361cellular_componentsuccinate-CoA ligase complex (ADP-forming)
E0016874molecular_functionligase activity
E0042709cellular_componentsuccinate-CoA ligase complex
E0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PO4 A 1600
ChainResidue
ASER153
AGLY154
ATHR155
AHIS246
ACOA1300
BGLY265
BALA266
BGLY267

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 1500
ChainResidue
AHOH1735
BMET1
BGLY220
BLEU223
BARG233
AARG243

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 B 1400
ChainResidue
BGLY52
BGLY53
BARG54
BGLY55
BASP213
BHOH1499

site_idAC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PO4 D 1601
ChainResidue
DSER153
DGLY154
DTHR155
DHIS246
EGLY265
EALA266
EGLY267

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 E 1401
ChainResidue
EGLY52
EGLY53
EARG54
EGLY55
EASP213
EHOH1523

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 E 1501
ChainResidue
DARG243
EMET1
EGLY220
EARG233
EHOH1583

site_idAC7
Number of Residues36
DetailsBINDING SITE FOR RESIDUE COA A 1300
ChainResidue
AGLY14
ATHR16
AGLY17
ASER18
AGLN19
AVAL38
ATHR39
APRO40
ALYS42
ATYR71
AVAL72
APRO73
APHE76
ASER80
AILE95
ATHR96
AGLU97
AASN122
ATHR123
APRO124
AILE136
APO41600
AHOH1703
AHOH1705
AHOH1706
AHOH1710
AHOH1766
AHOH1768
AHOH1777
BARG161
EARG29
EGLU33
ESER36
ELYS66
EHOH1504
EHOH1543

site_idAC8
Number of Residues9
DetailsBINDING SITE FOR RESIDUE COA B 1325
ChainResidue
BGLY320
BGLY321
BVAL323
BARG324
BCYS325
BILE328
BLEU349
BGLU350
BASN352

site_idAC9
Number of Residues33
DetailsBINDING SITE FOR RESIDUE COA D 1301
ChainResidue
DVAL72
DPRO73
DSER80
DILE95
DTHR96
DGLU97
DASN122
DPRO124
DILE136
DHOH1604
DHOH1606
DHOH1611
DHOH1618
DHOH1628
DHOH1640
DHOH1678
EARG161
BARG29
BGLU33
BSER36
BLYS66
BHOH1413
BHOH1486
DGLY14
DTHR16
DGLY17
DSER18
DGLN19
DVAL38
DTHR39
DPRO40
DLYS42
DTYR71

site_idBC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE COA E 1325
ChainResidue
EGLY320
EGLY321
EVAL323
EARG324
ECYS325
EILE328
ELEU349
EGLU350
EASN352

site_idBC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 1700
ChainResidue
AILE221
AVAL225
ALYS227
AVAL229
AALA268
AGLY269
AVAL270

Functional Information from PROSITE/UniProt
site_idPS00399
Number of Residues14
DetailsSUCCINYL_COA_LIG_2 ATP-citrate lyase / succinyl-CoA ligases family active site. GvtApkgk...RMGHAG
ChainResidueDetails
AGLY235-GLY248

site_idPS01216
Number of Residues30
DetailsSUCCINYL_COA_LIG_1 ATP-citrate lyase / succinyl-CoA ligases family signature 1. SRSGTLTyEavkqttdygfGqstcVGIGGD
ChainResidueDetails
ASER151-ASP180

site_idPS01217
Number of Residues26
DetailsSUCCINYL_COA_LIG_3 ATP-citrate lyase / succinyl-CoA ligases family signature 3. GnIgcMvNGAGLAmgtmDiVklhgGE
ChainResidueDetails
BGLY257-GLU282

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00558, ECO:0000269|PubMed:10625475
ChainResidueDetails
BLYS46
EGLU99
ETHR102
EGLU107
EASN199
EASP213
BGLY53
BGLU99
BTHR102
BGLU107
BASN199
BASP213
ELYS46
EGLY53

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00558
ChainResidueDetails
BASN264
BGLY321
EASN264
EGLY321
DGLY43
DTHR96

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01988
ChainResidueDetails
AGLU159
DGLU159

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1cqj
ChainResidueDetails
AGLU208
AHIS246
BTYR109
BGLU197

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1cqj
ChainResidueDetails
DGLU208
DHIS246
ETYR109
EGLU197

site_idMCSA1
Number of Residues2
DetailsM-CSA 476
ChainResidueDetails
BTYR109electrostatic stabiliser, steric role
BGLU197electrostatic stabiliser, modifies pKa

site_idMCSA2
Number of Residues2
DetailsM-CSA 476
ChainResidueDetails
ETYR109electrostatic stabiliser, steric role
EGLU197electrostatic stabiliser, modifies pKa

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PDB entries from 2024-07-24

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