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9GBN

Human Angiotensin-1 converting enzyme C-domain in complex with a diprolyl inhibitor- SG15

This is a non-PDB format compatible entry.
Functional Information from PROSITE/UniProt
site_idPS00142
Number of Residues10
DetailsZINC_PROTEASE Neutral zinc metallopeptidases, zinc-binding region signature. VAHHEMGHIQ
ChainResidueDetails
AVAL380-GLN389

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor 2 => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000269|PubMed:12540854, ECO:0000305|PubMed:16154999, ECO:0000305|PubMed:19773553
ChainResidueDetails
AGLU384

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor 2 => ECO:0000255|PROSITE-ProRule:PRU01355
ChainResidueDetails
AHIS513

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000269|PubMed:12540854
ChainResidueDetails
AARG186
ATYR224
ATRP485
AARG489

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000269|PubMed:12540854, ECO:0000269|PubMed:16476442, ECO:0000269|PubMed:23056909, ECO:0007744|PDB:4APH
ChainResidueDetails
AHIS383
AHIS387

site_idSWS_FT_FI5
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000269|PubMed:12540854, ECO:0000269|PubMed:16476442, ECO:0000269|PubMed:23056909, ECO:0000269|PubMed:7961923, ECO:0007744|PDB:4APH
ChainResidueDetails
AGLU411

site_idSWS_FT_FI6
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000269|PubMed:12540854, ECO:0000305|PubMed:11432860
ChainResidueDetails
AARG522

site_idSWS_FT_FI7
Number of Residues1
DetailsSITE: Cleavage => ECO:0000269|PubMed:7499427, ECO:0000269|PubMed:8253769
ChainResidueDetails
AARG561

site_idSWS_FT_FI8
Number of Residues1
DetailsSITE: Not glycosylated => ECO:0000269|PubMed:9013598
ChainResidueDetails
AASN620

site_idSWS_FT_FI9
Number of Residues1
DetailsSITE: Cleavage => ECO:0000269|PubMed:10769174
ChainResidueDetails
AARG627

site_idSWS_FT_FI10
Number of Residues1
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000269|PubMed:23056909, ECO:0007744|PDB:4APH
ChainResidueDetails
AASN72

site_idSWS_FT_FI11
Number of Residues1
DetailsCARBOHYD: N-linked (GlcNAc...) (complex) asparagine => ECO:0000269|PubMed:16335952, ECO:0000269|PubMed:9013598
ChainResidueDetails
AGLN90

site_idSWS_FT_FI12
Number of Residues1
DetailsCARBOHYD: N-linked (GlcNAc...) (complex) asparagine => ECO:0000269|PubMed:16335952, ECO:0000269|PubMed:19159218, ECO:0000269|PubMed:23056909, ECO:0000269|PubMed:9013598, ECO:0007744|PDB:4APH
ChainResidueDetails
AASN109

site_idSWS_FT_FI13
Number of Residues3
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine; partial => ECO:0000269|PubMed:9013598
ChainResidueDetails
AGLN155
AGLN337
AGLN586

Catalytic Information from CSA
site_idMCSA1
Number of Residues8
DetailsM-CSA 170
ChainResidueDetails
AHIS353electrostatic stabiliser, hydrogen bond acceptor
AALA354electrostatic stabiliser, hydrogen bond acceptor
AHIS383metal ligand
AGLU384electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AHIS387metal ligand
AGLU411metal ligand
AHIS513electrostatic stabiliser, hydrogen bond donor
ATYR523electrostatic stabiliser, hydrogen bond donor

230744

PDB entries from 2025-01-29

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