MolNFT v2 · #177277 · protein
7CGO: Cryo-EM structure of the flagellar motor-hook complex from Salmonella
7CGO · Flagellar basal-body rod protein FlgG: “Cryo-EM structure of the flagellar motor-hook complex from Salmonella”. Electron microscopy at 3.9, 20 pockets (best druggability 0.90). MolNFT v2 #177277 on GenesisL1: 3D structure, binding…

- PDB
- 7CGO
- Type
- protein
- Length
- 45,108 residues
- Chains
- 219
- Method
- electron microscopy
- Authors
- Tan, J.X., Chang, S.H., Wang, X.F., Xu, C.H., Zhou, Y., Zhang, X., Zhu, Y.Q.
- Deposited
- 07/01/20
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 3.9
- Source
- Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720)
- Molecule
- Flagellar basal-body rod protein FlgG; Flagellar basal-body rod protein FlgF; Flagellar…
- UniProt
- P0A1J3, P16323, P15928, P0A1I7, P16437, P26462, P0A1J1, P54702, P0A1L5, P54700, P0A1N8, P15930
- Pockets
- 20 · best druggability 0.90
Structure
electron microscopy · resolution 3.9 · 42 distinct chains · 36% helix, 23% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F, G, H, I, J, K, M | Flagellar basal-body rod protein FlgG | protein | 260 | 23% helix, 33% strand | P0A1J3 |
| L, U, V, W, X | Flagellar basal-body rod protein FlgG | protein | 259 | 24% helix, 33% strand | P0A1J3 |
| N | Flagellar basal-body rod protein FlgG | protein | 251 | 24% helix, 32% strand | P0A1J3 |
| O | Flagellar basal-body rod protein FlgG | protein | 252 | 22% helix, 33% strand | P0A1J3 |
| P | Flagellar basal-body rod protein FlgG | protein | 248 | 23% helix, 31% strand | P0A1J3 |
| Q, S | Flagellar basal-body rod protein FlgG | protein | 247 | 25% helix, 33% strand | P0A1J3 |
| R | Flagellar basal-body rod protein FlgG | protein | 250 | 23% helix, 32% strand | P0A1J3 |
| T | Flagellar basal-body rod protein FlgG | protein | 253 | 25% helix, 31% strand | P0A1J3 |
| a, c, d, e | Flagellar basal-body rod protein FlgF | protein | 249 | 28% helix, 30% strand | P16323 |
| b | Flagellar basal-body rod protein FlgF | protein | 248 | 28% helix, 25% strand | P16323 |
| 0, 1, 2, 3, 4, GI | Flagellar MS ring L2 | protein | 15 | 0% helix, 0% strand | — |
| 5, 6, 7, 9, 8 | Flagellar MS ring L1 | protein | 21 | 0% helix, 5% strand | P15928 |
| f | Flagellar basal-body rod protein FlgC | protein | 128 | 47% helix, 20% strand | P0A1I7 |
| g | Flagellar basal-body rod protein FlgC | protein | 130 | 49% helix, 18% strand | P0A1I7 |
| h | Flagellar basal-body rod protein FlgC | protein | 128 | 44% helix, 16% strand | P0A1I7 |
| j | Flagellar basal-body rod protein FlgC | protein | 127 | 48% helix, 17% strand | P0A1I7 |
| l, m | Flagellar basal body rod protein FlgB | protein | 106 | 64% helix, 5% strand | P16437 |
| o | Flagellar basal body rod protein FlgB | protein | 109 | 63% helix, 5% strand | P16437 |
| p | Flagellar basal-body rod protein FlgC | protein | 129 | 47% helix, 18% strand | P0A1I7 |
| i | Flagellar basal-body rod protein FlgC | protein | 129 | 44% helix, 16% strand | P0A1I7 |
| k | Flagellar basal body rod protein FlgB | protein | 108 | 62% helix, 5% strand | P16437 |
| n | Flagellar basal body rod protein FlgB | protein | 107 | 64% helix, 5% strand | P16437 |
| q | Flagellar hook-basal body complex protein FliE | protein | 71 | 80% helix, 0% strand | P26462 |
| r | Flagellar hook-basal body complex protein FliE | protein | 70 | 79% helix, 0% strand | P26462 |
| s, t, u | Flagellar hook-basal body complex protein FliE | protein | 72 | 82% helix, 0% strand | P26462 |
| v | Flagellar hook-basal body complex protein FliE | protein | 38 | 89% helix, 0% strand | P26462 |
| DA, DB, DC, DD, DE, DF, DG, DH, DI, DJ, DK, DL, DM, DN, DO, DP, DQ, DR, DS, DT, DU, DV, DW, DX, DY, DZ, EA, EB, EC, ED, EE, EF, EG | Flagellar hook protein FlgE | protein | 401 | 15% helix, 37% strand | P0A1J1 |
| CE | Flagellar biosynthetic protein FliR | protein | 260 | 70% helix, 0% strand | P54702 |
| CA, CB, CC, CD | Flagellar biosynthetic protein FliQ | protein | 89 | 80% helix, 0% strand | P0A1L5 |
| w, x, y, z, CF | Flagellar biosynthetic protein FliP | protein | 211 | 78% helix, 0% strand | P54700 |
| Da, Db, Dc, Dd, Dp, Dq, Dr, Ds, Dt, Du, Dv, Dw | Flagellar M-ring protein | protein | 109 | 29% helix, 14% strand | P15928 |
| De | Flagellar M-ring protein | protein | 99 | 32% helix, 15% strand | P15928 |
| Df, Do | Flagellar M-ring protein | protein | 97 | 29% helix, 15% strand | P15928 |
| Dg, Dh, Di, Dj, Dk, Dl, Dm, Dn | Flagellar M-ring protein | protein | 87 | 32% helix, 17% strand | P15928 |
| GA, GC | FlgB-Dc loop | protein | 11 | 0% helix, 0% strand | — |
| GF, GG, GH, GJ, GK | FliE helix 1 | protein | 18 | 89% helix, 0% strand | — |
| GE | FlgB-Dc loop | protein | 12 | 0% helix, 0% strand | — |
| GD | FlgB-Dc loop | protein | 10 | 0% helix, 0% strand | — |
| GB | FlgB-Dc loop | protein | 5 | 0% helix, 0% strand | — |
| Ca, Cb, Cc, Cd, Ce, Cf, Cg, Ch, Ci, Cj, Ck, Cl, Cm, Cn, Co, Cp, Cq, Cr, Cs, Ct, Cu, Cv, Cw, Cx, Cy, Cz, Ea, Eb, Ec, Ed, Ee, Ef, Eg, Eh | Flagellar M-ring protein | protein | 150 | 26% helix, 36% strand | P15928 |
| AA, AB, AC, AD, AE, AF, AG, AH, AI, AJ, AK, AL, AM, AN, AO, AP, AQ, AR, AS, AT, AU, AV, AW, AX, AY, AZ | Flagellar L-ring protein | protein | 211 | 14% helix, 45% strand | P0A1N8 |
| BA, BB, BC, BD, BE, BF, BG, BH, BI, BJ, BK, BL, BM, BN, BO, BP, BQ, BR, BS, BT, BU, BV, BW, BX, BY, BZ | Flagellar P-ring protein | protein | 303 | 22% helix, 31% strand | P15930 |
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 2119 | 0.90 | 0.91 | 246 | empty |
| 2 | 1021 | 0.89 | 0.91 | 119 | empty |
| 3 | 1154 | 0.89 | 0.91 | 126 | empty |
| 4 | 617 | 0.89 | 0.93 | 56 | empty |
| 5 | 1332 | 0.89 | 0.90 | 156 | empty |
Interfaces
886 interfaces between chains.
- BY–BZ · 3520 Ų buried · 40 hydrogen bonds · protein-protein
- BQ–BR · 3482 Ų buried · 45 hydrogen bonds · protein-protein
- BK–BL · 3481 Ų buried · 39 hydrogen bonds · protein-protein
- BO–BP · 3481 Ų buried · 40 hydrogen bonds · protein-protein
- BX–BY · 3477 Ų buried · 39 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 26 disulfide, 26 modified (disulfide, nonstandard).
Compared structures
- P0A1J3 · AlphaFold monomer V2.0 prediction for flagellar basal-body rod protein flgg (P0A1J3) · a predicted model of the same protein · chain F against A, TM-score 0.97
- P15928 · AlphaFold monomer V2.0 prediction for flagellar M-ring protein (P15928) · a predicted model of the same protein · chain Dl against A, TM-score 0.96
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 P0A1J3
- Every structure of UniProt P16323
- Every structure of UniProt P15928
- Every structure of UniProt P0A1I7
- Every structure of UniProt P16437
- Every structure of UniProt P26462
- Every structure of UniProt P0A1J1
- Every structure of UniProt P54702
- Every structure of UniProt P0A1L5
- Every structure of UniProt P54700
- Every structure of UniProt P0A1N8
- Every structure of UniProt P15930
- Elsewhere: RCSB PDB 7CGO · PDBe 7CGO · UniProt P0A1J3 · UniProt P16323 · UniProt P15928 · UniProt P0A1I7 · UniProt P16437 · UniProt P26462 · UniProt P0A1J1 · UniProt P54702 · UniProt P0A1L5 · UniProt P54700 · UniProt P0A1N8 · UniProt P15930
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