Research workbench
Fe protein independent substrate reduction by nitrogenase variants altered in intramolecular electron transfer
Analyse Fe protein independent substrate reduction by nitrogenase variants altered in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4XPI
- Type
- protein
- Length
- 2,001 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Nitrogenase molybdenum-iron protein alpha chain; Nitrogenase molybdenum-iron protein beta…
- EC
- 1.18.6.1
- UniProt
- P07328, P07329
- Ligands
- HCA, ICS, 1CL, CA
- Pockets
- 20 · best druggability 0.88
Structure
x-ray diffraction · 3 distinct chains · 50% helix, 13% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Nitrogenase molybdenum-iron protein alpha chain (EC 1.18.6.1) | protein | 479 | 49% helix, 15% strand | P07328 |
| B, D | Nitrogenase molybdenum-iron protein beta chain (EC 1.18.6.1) | protein | 522 | 52% helix, 11% strand | P07329 |
| C | Nitrogenase molybdenum-iron protein alpha chain (EC 1.18.6.1) | protein | 478 | 48% helix, 14% strand | P07328 |
Ligands and binding sites
- HCA · 3-hydroxy-3-carboxy-adipic acid · ligand · 2 copies · chains A, C
- ICS · iron-sulfur-molybdenum cluster with interstitial carbon · ligand · 2 copies · chains A, C
- 1CL · FE(8)-S(7) cluster, oxidized · ligand · 2 copies · chains A, B, C, D
- CA · Calcium ion · metal · 2 copies · chains B, C, D, A
- GOL · Glycerol · additive · 15 copies · chains A, B, D, C
- TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · 2 copies · chains B, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 587 | 0.88 | 0.94 | 81 | HCA, ICS |
| 2 | 577 | 0.88 | 0.94 | 81 | HCA, ICS, GOL |
| 3 | 920 | 0.86 | 0.87 | 71 | GOL |
| 4 | 101 | 0.77 | 0.97 | 29 | GOL |
| 5 | 98 | 0.76 | 0.97 | 30 | GOL |
Interfaces
5 interfaces between chains.
- C–D · 4693 Ų buried · 56 hydrogen bonds · protein-protein
- A–B · 4692 Ų buried · 56 hydrogen bonds · protein-protein
- B–D · 3158 Ų buried · 60 hydrogen bonds · protein-protein
- A–D · 1366 Ų buried · 16 hydrogen bonds · protein-protein
- B–C · 1363 Ų buried · 15 hydrogen bonds · protein-protein
Compared structures
- 4XPI · Fe protein independent substrate reduction by nitrogenase variants altered in… · the same entry in another collection · chain A against A, TM-score 1.00
- P07328 · AlphaFold monomer V2.0 prediction for nitrogenase molybdenum-iron protein alpha chain… · a predicted model of the same protein · chain C against A, TM-score 1.00
- P07329 · AlphaFold monomer V2.0 prediction for nitrogenase molybdenum-iron protein beta chain… · a predicted model of the same protein · chain B against A, TM-score 1.00
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 P07328
- Every structure of UniProt P07329
- Elsewhere: RCSB PDB 4XPI · PDBe 4XPI · UniProt P07328 · UniProt P07329
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