Research workbench
The structure of human prolylcarboxypeptidase at 2.80 ångströms resolution
Analyse The structure of human prolylcarboxypeptidase at 2.80 ångströms resolution in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3N2Z
- Type
- protein
- Length
- 442 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P42785
Structure
x-ray diffraction · 1 distinct chain.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | — | protein | 442 | — | P42785 |
Compared structures
- 3N2Z · The Structure of Human Prolylcarboxypeptidase at 2.80 Angstroms Resolution · the same entry in another collection · chain B against B, TM-score 1.00
- P42785 · AlphaFold monomer V2.0 prediction for lysosomal pro-X carboxypeptidase (P42785) · a predicted model of the same protein · chain B against A, TM-score 0.99
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P42785
- Elsewhere: RCSB PDB 3N2Z · PDBe 3N2Z · UniProt P42785
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