1LYB | pdb_00001lyb

CRYSTAL STRUCTURES OF NATIVE AND INHIBITED FORMS OF HUMAN CATHEPSIN D: IMPLICATIONS FOR LYSOSOMAL TARGETING AND DRUG DESIGN


Domain Annotation: SCOP/SCOPe Classification SCOP-e Database Homepage

ChainsDomain InfoClassFoldSuperfamilyFamilyDomainSpeciesProvenance Source (Version)
Bd1lyb.1 All beta proteins Acid proteases Acid proteases Pepsin-like Cathepsin D (Homo sapiens ) [TaxId: 9606 ], SCOPe (2.08)
E [auth D]d1lyb.2 All beta proteins Acid proteases Acid proteases Pepsin-like Cathepsin D (Homo sapiens ) [TaxId: 9606 ], SCOPe (2.08)
Ad1lyb.1 All beta proteins Acid proteases Acid proteases Pepsin-like Cathepsin D (Homo sapiens ) [TaxId: 9606 ], SCOPe (2.08)
D [auth C]d1lyb.2 All beta proteins Acid proteases Acid proteases Pepsin-like Cathepsin D (Homo sapiens ) [TaxId: 9606 ], SCOPe (2.08)

Domain Annotation: CATH CATH Database Homepage

ChainDomainClassArchitectureTopologyHomologyProvenance Source (Version)
B2.40.70.10 Mainly Beta Beta Barrel Cathepsin D, subunit A domain 1CATH (4.3.0)
E [auth D]2.40.70.10 Mainly Beta Beta Barrel Cathepsin D, subunit A domain 1CATH (4.3.0)
A2.40.70.10 Mainly Beta Beta Barrel Cathepsin D, subunit A domain 1CATH (4.3.0)
D [auth C]2.40.70.10 Mainly Beta Beta Barrel Cathepsin D, subunit A domain 1CATH (4.3.0)

Protein Family Annotation Pfam Database Homepage

ChainsAccessionNameDescriptionCommentsSource
B,
E [auth D]
PF00026Eukaryotic aspartyl protease (Asp)Eukaryotic aspartyl proteaseAspartyl (acid) proteases include pepsins, cathepsins, and renins. Two-domain structure, probably arising from ancestral duplication. This family does not include the retroviral nor retrotransposon proteases (Pfam:PF00077), which are much smaller a ...Aspartyl (acid) proteases include pepsins, cathepsins, and renins. Two-domain structure, probably arising from ancestral duplication. This family does not include the retroviral nor retrotransposon proteases (Pfam:PF00077), which are much smaller and appear to be homologous to a single domain of the eukaryotic asp proteases.
Domain

Gene Ontology: Gene Product Annotation Gene Ontology Database Homepage

ChainsPolymerMolecular FunctionBiological ProcessCellular Component
B,
E [auth D]
CATHEPSIN D
A,
D [auth C]
CATHEPSIN D
C [auth I],
F [auth J]
PEPSTATIN---

Pharos: Disease Associations Pharos Homepage Annotation

ChainsDrug Target  Associated Disease
B,
E [auth D]
PharosP07339
A,
D [auth C]
PharosP07339