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3HH3

New azaborine compounds bind to the T4 lysozyme L99A cavity - 1,2-dihydro-1,2-azaborine

Functional Information from GO Data
ChainGOidnamespacecontents
A0003796molecular_functionlysozyme activity
A0009253biological_processpeptidoglycan catabolic process
A0016798molecular_functionhydrolase activity, acting on glycosyl bonds
A0016998biological_processcell wall macromolecule catabolic process
A0030430cellular_componenthost cell cytoplasm
A0031640biological_processkilling of cells of another organism
A0042742biological_processdefense response to bacterium
A0044659biological_processviral release from host cell by cytolysis
Functional Information from PDB Data
site_idAC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE HED A 165
ChainResidue
AILE3
AASN68
AASP72
AVAL75
AARG76
ATYR88
AALA93
AILE100

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE HED A 166
ChainResidue
ALEU32
AASP70
AVAL103
APHE104
AHOH198
AHOH221
AHOH222
AGLY30

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE PO4 A 167
ChainResidue
AARG14
ALYS19
AARG125
ATRP126
AASP127
AGLU128
AHOH190
AHOH240
AHOH337

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE NA A 168
ChainResidue
AGLU11
ATYR18
AHOH202
AHOH233
AHOH282
AHOH358

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE B20 A 169
ChainResidue
AVAL87
AALA99
AVAL111
ALEU118
APHE153

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton donor/acceptor => ECO:0000255|HAMAP-Rule:MF_04110, ECO:0000269|PubMed:3382407, ECO:0000269|PubMed:7831309, ECO:0000269|PubMed:8266098
ChainResidueDetails
AGLU11

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor/acceptor => ECO:0000255|HAMAP-Rule:MF_04110, ECO:0000269|PubMed:1892846, ECO:0000269|PubMed:3382407, ECO:0000269|PubMed:7831309, ECO:0000269|PubMed:8266098
ChainResidueDetails
AASP20

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:8266098
ChainResidueDetails
ALEU32
APHE104

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000303|PubMed:7831309
ChainResidueDetails
ASER117
AASN132

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 206l
ChainResidueDetails
AGLU11
AASP20

site_idMCSA1
Number of Residues2
DetailsM-CSA 921
ChainResidueDetails
AGLU11proton shuttle (general acid/base)
AASP20covalent catalysis

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PDB entries from 2024-05-01

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