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1DI1

CRYSTAL STRUCTURE OF ARISTOLOCHENE SYNTHASE FROM PENICILLIUM ROQUEFORTI

Functional Information from PROSITE/UniProt
site_idPS00142
Number of Residues10
DetailsZINC_PROTEASE Neutral zinc metallopeptidases, zinc-binding region signature. LSIHELGHYL
ChainResidueDetails
ALEU188-LEU197

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10825154, ECO:0007744|PDB:1DGP
ChainResidueDetails
BASP115
BASN244
AASP115
AASN244

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:Q9UR08
ChainResidueDetails
BLYS251
BGLU252
ASER248
AARG200
ALYS251
AGLU252
BARG200
BSER248

site_idSWS_FT_FI3
Number of Residues8
DetailsSITE: Important for catalytic activity => ECO:0000269|PubMed:10825154, ECO:0007744|PDB:1DI1
ChainResidueDetails
BTYR92
BPHE112
BPHE178
BTRP333
ATYR92
APHE112
APHE178
ATRP333

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 261
ChainResidueDetails
ATYR92electrostatic stabiliser, steric role, van der waals interaction
APHE112electrostatic stabiliser, steric role, van der waals interaction
APHE178electrostatic stabiliser, steric role, van der waals interaction
ALYS206hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
ATRP333electrostatic stabiliser, steric role, van der waals interaction

site_idMCSA2
Number of Residues5
DetailsM-CSA 261
ChainResidueDetails
BTYR92electrostatic stabiliser, steric role, van der waals interaction
BPHE112electrostatic stabiliser, steric role, van der waals interaction
BPHE178electrostatic stabiliser, steric role, van der waals interaction
BLYS206hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BTRP333electrostatic stabiliser, steric role, van der waals interaction

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PDB entries from 2024-04-17

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