Generated by analyze.py. Do not hand-edit — rerun uv run python analyze.py.
Contact residues were derived from PDB 9B85 (cryo-EM structure of human dynactin bound to the Chlamydia effector Dre1, released 2025-04-16), not recited for conventional actin by analogy.
All 8 Arp1 filament protomers in that entry (chains A, B, C, D, E, F, G, I) are modelled as ACTR1A / alpha-centractin, each with a bound ADP. ACTR1B is assigned to 0 chains of 9B85 by SIFTS, and PDBe maps 0 PDB entries to P42025 in total — i.e. ACTR1B is present in no deposited structure at all, so its residues are tested by alignment onto the ACTR1A protomer.
Cutoff: heavy-atom contacts within 4.0 A. Reference chain A maps 1:1 onto P61163 residues 1-376 by SIFTS (re-verified at runtime).
| Accession | Role | Len | % id to ACTR1A | Nucleotide site | Protomer interface |
|---|---|---|---|---|---|
| P42025 | ACTR1B human (beta-centractin) -- the gene under review | 376 | 90.4 | 17/18 | 32/37 |
| P61163 | ACTR1A human (alpha-centractin) -- paralog, modelled in 9B85 | 376 | 100.0 | 18/18 | 37/37 |
| F2Z5G5 | ACTR1A pig -- WITH/FROM donor on the IBA rows | 349 | 90.3 | 17/18 | 37/37 |
| O94630 | arp1 S. pombe -- WITH/FROM donor (sole donor for GO:0106006) | 379 | 52.0 | 13/18 | 20/37 |
| P38696 | ARP1 S. cerevisiae -- WITH/FROM donor | 384 | 53.2 | 10/18 | 20/37 |
| Q9NA98 | arp-1 C. elegans -- WITH/FROM donor (TrEMBL) | 374 | 70.3 | 14/18 | 27/37 |
| Q5BBX7 | AN1953 A. nidulans -- WITH/FROM donor (TrEMBL) | 380 | 63.8 | 12/18 | 25/37 |
| Q8R5C5 | Actr1b mouse -- ortholog of the gene under review | 376 | 91.2 | 17/18 | 32/37 |
| P60709 | ACTB human (beta-actin) -- conventional actin outgroup | 375 | 53.6 | 11/18 | 16/37 |
| Q9NZ32 | ACTR10 human (Arp11) -- dynactin pointed-end capping Arp | 417 | 29.5 | 6/18 | 10/37 |
6 of 55 contact positions differ. 6/6 are conserved in the mouse ACTR1B orthologue (Q8R5C5), so they are fixed features of the beta paralog rather than human-specific noise. At 4/6 the ACTR1B residue is independently present in another Arp1 family member or in conventional actin -- a position the family already tolerates, not a novel loss. The two counts are kept separate because a substitution shared only with the mouse orthologue is not independent evidence of tolerance.
| Set | Pos | ACTR1A | ACTR1B | F2Z5G5 | O94630 | P38696 | Q9NA98 | Q5BBX7 | Q8R5C5 | P60709 | Q9NZ32 | family members (excl. mouse ACTR1B) sharing it |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nucleotide_site | 215 | K | R | K | R | R | R | R | R | R | E | O94630, P38696, P60709, Q5BBX7, Q9NA98 |
| protomer_interface | 45 | V | M | V | E | D | H | P | M | Q | V | none |
| protomer_interface | 197 | Y | L | Y | Q | Q | L | L | L | I | Q | Q5BBX7, Q9NA98 |
| protomer_interface | 207 | S | T | S | S | S | R | T | T | T | V | P60709, Q5BBX7 |
| protomer_interface | 213 | I | V | I | I | I | I | V | V | I | V | Q5BBX7, Q9NZ32 |
| protomer_interface | 268 | I | V | I | M | I | I | I | V | L | - | none |
nucleotide_site: G17, S18, G19, V20, K22, G161, D162, G163, G187, S191, K215, K218, E219, G303, S304, L306, F307, L337
protomer_interface: P42, K43, H44, V45, R46, V47, M48, A49, G50, A51, L52, H65, R66, G67, L68, Y197, R199, K200, E201, G202, F205, H206, S207, S208, E210, I213, K238, L243, P244, D245, G246, S247, P253, D266, L267, I268, G269