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1H1T

PHOSPHOPANTETHEINE ADENYLYLTRANSFERASE IN COMPLEX WITH Coenzyme A FROM ESCHERICHIA COLI

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004595molecular_functionpantetheine-phosphate adenylyltransferase activity
A0005515molecular_functionprotein binding
A0005524molecular_functionATP binding
A0005737cellular_componentcytoplasm
A0009058biological_processbiosynthetic process
A0015937biological_processcoenzyme A biosynthetic process
A0016779molecular_functionnucleotidyltransferase activity
A0042802molecular_functionidentical protein binding
B0003824molecular_functioncatalytic activity
B0004595molecular_functionpantetheine-phosphate adenylyltransferase activity
B0005515molecular_functionprotein binding
B0005524molecular_functionATP binding
B0005737cellular_componentcytoplasm
B0009058biological_processbiosynthetic process
B0015937biological_processcoenzyme A biosynthetic process
B0016779molecular_functionnucleotidyltransferase activity
B0042802molecular_functionidentical protein binding
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A1161
ChainResidue
ASER121
ALYS122
AHOH2139
AHOH2140
AHOH2141
BHIS104
BARG107

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 B1160
ChainResidue
BSER121
BLYS122
BHOH2137
BHOH2138
BHOH2139
AHIS104
AARG107

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 B1161
ChainResidue
BHIS18
BARG91
BSER128
BSER129
BHOH2015
BHOH2140

site_idAC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 B1162
ChainResidue
BSER39
BPRO40
BSER41
BARG137
BHIS138
BHOH2142
BHOH2143

site_idAC5
Number of Residues22
DetailsBINDING SITE FOR RESIDUE COA A1160
ChainResidue
APRO8
AGLY9
ATHR10
AASP72
ALEU73
AMET74
AARG88
AARG91
AALA94
AASP95
ATYR98
AGLU99
ALEU102
AASN106
AGLU134
AHIS138
AHOH2080
AHOH2109
AHOH2135
AHOH2136
AHOH2137
AHOH2138

site_idAC6
Number of Residues14
DetailsBINDING SITE FOR RESIDUE PNS B1163
ChainResidue
BGLY9
BTHR10
BLYS42
BLEU73
BMET74
BARG88
BMET105
BASN106
BGLU134
BHIS138
BHOH2088
BHOH2142
BHOH2144
BHOH2145

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:11812124, ECO:0000269|PubMed:12837781, ECO:0007744|PDB:1H1T, ECO:0007744|PDB:1QJC
ChainResidueDetails
ATHR10
ALYS42
AMET74
BTHR10
BLYS42
BMET74

site_idSWS_FT_FI2
Number of Residues10
DetailsBINDING: BINDING => ECO:0000269|PubMed:11812124, ECO:0007744|PDB:1GN8
ChainResidueDetails
AHIS18
BTYR7
AGLY89
AGLU99
ATRP124
BHIS18
BGLY89
BGLU99
BTRP124
ATYR7

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:11812124, ECO:0007744|PDB:1QJC
ChainResidueDetails
AARG88
BARG88

site_idSWS_FT_FI4
Number of Residues2
DetailsSITE: Transition state stabilizer => ECO:0000305|PubMed:11812124
ChainResidueDetails
AHIS18
BHIS18

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 299
ChainResidueDetails
AHIS18electrostatic stabiliser, hydrogen bond donor
ALYS42attractive charge-charge interaction, electrostatic stabiliser
AARG91attractive charge-charge interaction, electrostatic stabiliser
ASER129electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues4
DetailsM-CSA 299
ChainResidueDetails
BHIS18electrostatic stabiliser, hydrogen bond donor
BLYS42attractive charge-charge interaction, electrostatic stabiliser
BARG91attractive charge-charge interaction, electrostatic stabiliser
BSER129electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2024-07-24

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