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5TH6

Structure determination of a potent, selective antibody inhibitor of human MMP9 (apo MMP9)

Functional Information from GO Data
ChainGOidnamespacecontents
A0004222molecular_functionmetalloendopeptidase activity
A0006508biological_processproteolysis
A0008237molecular_functionmetallopeptidase activity
A0008270molecular_functionzinc ion binding
A0031012cellular_componentextracellular matrix
B0004222molecular_functionmetalloendopeptidase activity
B0006508biological_processproteolysis
B0008237molecular_functionmetallopeptidase activity
B0008270molecular_functionzinc ion binding
B0031012cellular_componentextracellular matrix
C0004222molecular_functionmetalloendopeptidase activity
C0006508biological_processproteolysis
C0008237molecular_functionmetallopeptidase activity
C0008270molecular_functionzinc ion binding
C0031012cellular_componentextracellular matrix
D0004222molecular_functionmetalloendopeptidase activity
D0006508biological_processproteolysis
D0008237molecular_functionmetallopeptidase activity
D0008270molecular_functionzinc ion binding
D0031012cellular_componentextracellular matrix
Functional Information from PDB Data
site_idAC1
Number of Residues4
Detailsbinding site for residue ZN A 501
ChainResidue
ACYS99
AHIS401
AHIS405
AHIS411

site_idAC2
Number of Residues4
Detailsbinding site for residue ZN A 502
ChainResidue
AHIS175
AASP177
AHIS190
AHIS203

site_idAC3
Number of Residues6
Detailsbinding site for residue CA A 503
ChainResidue
AGLY197
AGLN199
AASP201
AHOH610
AHOH629
AASP165

site_idAC4
Number of Residues6
Detailsbinding site for residue CA A 504
ChainResidue
AASP182
AGLY183
AASP185
ALEU187
AASP205
AGLU208

site_idAC5
Number of Residues4
Detailsbinding site for residue CA A 505
ChainResidue
AASP131
AASP206
AGLU208
AHOH648

site_idAC6
Number of Residues4
Detailsbinding site for residue ZN B 501
ChainResidue
BCYS99
BHIS401
BHIS405
BHIS411

site_idAC7
Number of Residues4
Detailsbinding site for residue ZN B 502
ChainResidue
BHIS175
BASP177
BHIS190
BHIS203

site_idAC8
Number of Residues6
Detailsbinding site for residue CA B 503
ChainResidue
BASP165
BGLY197
BGLN199
BASP201
BHOH613
BHOH642

site_idAC9
Number of Residues6
Detailsbinding site for residue CA B 504
ChainResidue
BASP182
BGLY183
BASP185
BLEU187
BASP205
BGLU208

site_idAD1
Number of Residues3
Detailsbinding site for residue CA B 505
ChainResidue
BASP131
BASP206
BGLU208

site_idAD2
Number of Residues4
Detailsbinding site for residue ZN C 501
ChainResidue
CCYS99
CHIS401
CHIS405
CHIS411

site_idAD3
Number of Residues4
Detailsbinding site for residue ZN C 502
ChainResidue
CHIS175
CASP177
CHIS190
CHIS203

site_idAD4
Number of Residues6
Detailsbinding site for residue CA C 503
ChainResidue
CASP165
CGLY197
CGLN199
CASP201
CHOH632
CHOH656

site_idAD5
Number of Residues6
Detailsbinding site for residue CA C 504
ChainResidue
CASP182
CGLY183
CASP185
CLEU187
CASP205
CGLU208

site_idAD6
Number of Residues5
Detailsbinding site for residue CA C 505
ChainResidue
CASP131
CASP206
CGLU208
CHOH617
CHOH783

site_idAD7
Number of Residues4
Detailsbinding site for residue ZN D 501
ChainResidue
DCYS99
DHIS401
DHIS405
DHIS411

site_idAD8
Number of Residues4
Detailsbinding site for residue ZN D 502
ChainResidue
DHIS175
DASP177
DHIS190
DHIS203

site_idAD9
Number of Residues6
Detailsbinding site for residue CA D 503
ChainResidue
DASP165
DGLY197
DGLN199
DASP201
DHOH640
DHOH653

site_idAE1
Number of Residues6
Detailsbinding site for residue CA D 504
ChainResidue
DASP182
DGLY183
DASP185
DLEU187
DASP205
DGLU208

site_idAE2
Number of Residues4
Detailsbinding site for residue CA D 505
ChainResidue
DASP131
DASP206
DGLU208
DHOH635

Functional Information from PROSITE/UniProt
site_idPS00142
Number of Residues10
DetailsZINC_PROTEASE Neutral zinc metallopeptidases, zinc-binding region signature. VAAHEFGHAL
ChainResidueDetails
AVAL398-LEU407

site_idPS00546
Number of Residues8
DetailsCYSTEINE_SWITCH Matrixins cysteine switch. PRCGvPDL
ChainResidueDetails
APRO97-LEU104

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues28
DetailsMotif: {"description":"Cysteine switch","evidences":[{"source":"PubMed","id":"12077439","evidenceCode":"ECO:0000303"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues4
DetailsActive site: {"evidences":[{"source":"PubMed","id":"12051944","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsBinding site: {"description":"in inhibited form","evidences":[{"source":"PubMed","id":"12051944","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"12077439","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues48
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"12051944","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues28
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"12051944","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"12077439","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues4
DetailsSite: {"description":"Cleavage; by MMP3","evidences":[{"source":"PubMed","id":"1371271","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues8
DetailsGlycosylation: {"description":"N-linked (GlcNAc...) asparagine","evidences":[{"evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

243911

PDB entries from 2025-10-29

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