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8WBZ

Cryo-EM structure of ACE2-B0AT1 complex with JX225

Functional Information from PROSITE/UniProt
site_idPS00142
Number of Residues10
DetailsZINC_PROTEASE Neutral zinc metallopeptidases, zinc-binding region signature. TAHHEMGHIQ
ChainResidueDetails
BTHR371-GLN380

site_idPS00610
Number of Residues15
DetailsNA_NEUROTRAN_SYMP_1 Sodium:neurotransmitter symporter family signature 1. WRFPYlcqsHGGGaF
ChainResidueDetails
ATRP56-PHE70

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1444
DetailsTOPO_DOM: Extracellular => ECO:0000255
ChainResidueDetails
BGLN18-SER740
CGLN18-SER740

site_idSWS_FT_FI2
Number of Residues40
DetailsTRANSMEM: Helical => ECO:0000255|PROSITE-ProRule:PRU01354
ChainResidueDetails
BILE741-ILE761
DGLY326-SER413
DGLY478-GLY490
DGLU553-TRP581
CILE741-ILE761
ATHR243-TRP268
AGLY326-SER413
AGLY478-GLY490
AGLU553-TRP581
DGLN63-GLY67
DASN142-SER192
DTHR243-TRP268

site_idSWS_FT_FI3
Number of Residues86
DetailsTOPO_DOM: Cytoplasmic => ECO:0000255
ChainResidueDetails
BPHE762-PHE805
CPHE762-PHE805

site_idSWS_FT_FI4
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000305|PubMed:14754895, ECO:0000305|PubMed:27217402
ChainResidueDetails
BGLU375
DASN435-GLU456
DASP512-GLN531
DTYR603-TYR634
CGLU375
ASER290-VAL304
AASN435-GLU456
AASP512-GLN531
ATYR603-TYR634
DGLU89-LEU120
DARG214-LYS221
DSER290-VAL304

site_idSWS_FT_FI5
Number of Residues2
DetailsACT_SITE: Proton donor => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000305|PubMed:14754895
ChainResidueDetails
BHIS505
CHIS505

site_idSWS_FT_FI6
Number of Residues6
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000269|PubMed:14754895, ECO:0000305|PubMed:19021774
ChainResidueDetails
BARG169
BTRP477
BLYS481
CARG169
CTRP477
CLYS481

site_idSWS_FT_FI7
Number of Residues6
DetailsBINDING: BINDING => ECO:0000305|PubMed:14754895
ChainResidueDetails
BARG273
BHIS345
BTYR515
CARG273
CHIS345
CTYR515

site_idSWS_FT_FI8
Number of Residues6
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU01355, ECO:0000269|PubMed:14754895
ChainResidueDetails
BHIS374
BHIS378
BGLU402
CHIS374
CHIS378
CGLU402

site_idSWS_FT_FI9
Number of Residues2
DetailsMOD_RES: Phosphotyrosine => ECO:0000305|PubMed:33436497, ECO:0000305|PubMed:33436498
ChainResidueDetails
BTYR781
CTYR781

site_idSWS_FT_FI10
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000305|PubMed:33436497, ECO:0000305|PubMed:33436498
ChainResidueDetails
BSER783
CSER783

site_idSWS_FT_FI11
Number of Residues4
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000305|PubMed:14754895
ChainResidueDetails
BASN53
BASN322
CASN53
CASN322

site_idSWS_FT_FI12
Number of Residues2
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000269|PubMed:14754895, ECO:0000269|PubMed:15084671, ECO:0000269|PubMed:19901337
ChainResidueDetails
BASN90
CASN90

site_idSWS_FT_FI13
Number of Residues4
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000269|PubMed:14754895
ChainResidueDetails
BASN103
BASN432
CASN103
CASN432

site_idSWS_FT_FI14
Number of Residues2
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000269|PubMed:14754895, ECO:0000269|PubMed:19159218, ECO:0000269|PubMed:19901337
ChainResidueDetails
BASN546
CASN546

site_idSWS_FT_FI15
Number of Residues2
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
BASN690
CASN690
DSER17
DSER627

site_idSWS_FT_FI16
Number of Residues4
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin) => ECO:0000269|PubMed:36876523
ChainResidueDetails
BLYS788
DASN368
AASN182
CLYS788
AASN354
AASN368
DASN158
DASN182
DASN258
DASN354

225946

PDB entries from 2024-10-09

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