P77774: Outer membrane protein assembly factor BamB (bamB)

Outer membrane protein assembly factor BamB (bamB) is a 392-residue protein from Escherichia coli (strain K12). This is its AlphaFold structure prediction, created 1 Aug 2025. UniProt accession: P77774.

Gene
bamB
Organism
Escherichia coli (strain K12)
Length
392 residues
Mean pLDDT
88.8
Model
AF-P77774-F1 v6
Model created
1 Aug 2025
PDB structures
92

Explore in 3D Color by confidence AlphaFold DB UniProt

Model confidence (pLDDT)

The mean pLDDT of this model is 88.8 (confident overall). pLDDT is AlphaFold's per-residue confidence score from 0 to 100. In MolViewer, choose the B-factor color scheme to color the model by pLDDT, because AlphaFold stores it in the B-factor column.

pLDDT bandMeaningShare of residues
Above 90Very high: backbone and side chains are usually accurate74%
70 to 90Confident: backbone generally right13%
50 to 70Low: treat with caution10%
Below 50Very low: often disordered regions3%

What pLDDT means and how to read it

Function

Part of the outer membrane protein assembly complex (Bam), which is involved in assembly and insertion of beta-barrel proteins into the outer membrane. Nonessential member of the complex, which may orient the flexible periplasmic domain of BamA for interaction with other Bam components, chaperones and nascent outer membrane proteins. Efficient substrate folding and insertion into the outer membrane requires all 5 subunits (PubMed:20378773, PubMed:21823654, PubMed:27686148). A lateral gate may open between the first and last strands of the BamA beta-barrel that allows substrate to insert into the outer membrane; comparison of the structures of complete and nearly complete Bam complexes show…

Subunit structure

Part of the Bam complex, which is composed of the outer membrane protein BamA, and four lipoproteins BamB, BamC, BamD and BamE. Monomer. Interacts directly with BamA. The Bam complex has the shape of a hat, with the BamA beta-barrel crown in the outer membrane and the periplasmic brim formed by the BamA POTRA domains and the 4 lipoproteins (PubMed:26900875, PubMed:26901871, PubMed:27686148)

Subcellular location

Cell outer membrane

Experimental structures in the PDB

Compare the prediction with experimentally determined structures of the same protein:

PDB IDMethodResolutionChains and residues
3Q7MX-ray1.65 ÅA=21-392
3Q7NX-ray1.77 ÅA=21-392
3PRWX-ray1.8 ÅA=21-392
3Q7OX-ray2.09 ÅA=21-392
2YMSX-ray2.1 ÅA=62-191, B=113-186, C=248-322, D=247-320
4XGAX-ray2.15 ÅA=20-392
2YH3X-ray2.6 ÅA=22-392
3P1LX-ray2.6 ÅA=21-392
9CNWEM2.6 ÅB=1-392
9HG6EM2.73 ÅB=20-392
9HG5EM2.82 ÅB=20-392
9HG7EM2.83 ÅB=20-392
9HG9EM2.88 ÅB=20-392
5D0OX-ray2.9 ÅB=1-392
8PZVEM2.9 ÅB=20-392
9HG8EM2.9 ÅB=20-392
8ADGEM3.0 ÅB=1-392
9HE1EM3.0 ÅB=1-392
7NRIEM3.03 ÅB=20-392
6LYSX-ray3.05 ÅB=1-392

Showing 20 of 92 experimental structures (best resolution first).

More AlphaFold highlights

About this viewer

MolViewer loads the AlphaFold model straight from AlphaFold DB into your browser. Show it as a cartoon, color by pLDDT, measure distances and angles, and load a PDB structure next to it to compare.