A family of very long coiled-coil proteins, likely performing cytoskeletal functions.. Two varieties have evolved, one with an N-terminal FYVE domain (Non-TM) and another with a C-terminal PDZ domain (might be TM)
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 0 |
| Forrest at al. (procyclic) | no | yes: 0 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | yes | yes: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 5 |
| NetGPI | no | yes: 0, no: 5 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AD01
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.597 |
| CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.594 |
| CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.551 |
| CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.558 |
| CLV_PCSK_PC7_1 | 21 | 27 | PF00082 | 0.558 |
| DOC_MAPK_gen_1 | 25 | 32 | PF00069 | 0.556 |
| LIG_FHA_1 | 50 | 56 | PF00498 | 0.517 |
| LIG_FHA_2 | 29 | 35 | PF00498 | 0.561 |
| LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.579 |
| LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.581 |
| LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.540 |
| MOD_CK1_1 | 10 | 16 | PF00069 | 0.604 |
| MOD_CK2_1 | 17 | 23 | PF00069 | 0.570 |
| MOD_CK2_1 | 28 | 34 | PF00069 | 0.549 |
| MOD_GSK3_1 | 17 | 24 | PF00069 | 0.582 |
| MOD_GSK3_1 | 2 | 9 | PF00069 | 0.606 |
| MOD_GSK3_1 | 44 | 51 | PF00069 | 0.549 |
| MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.560 |
| MOD_PKA_2 | 2 | 8 | PF00069 | 0.588 |
| MOD_PKA_2 | 44 | 50 | PF00069 | 0.558 |
| MOD_Plk_1 | 28 | 34 | PF00069 | 0.564 |
| TRG_DiLeu_BaEn_4 | 110 | 116 | PF01217 | 0.466 |
| TRG_DiLeu_BaEn_4 | 120 | 126 | PF01217 | 0.435 |
| TRG_DiLeu_BaEn_4 | 130 | 136 | PF01217 | 0.442 |
| TRG_DiLeu_BaEn_4 | 140 | 146 | PF01217 | 0.436 |
| TRG_DiLeu_BaEn_4 | 170 | 176 | PF01217 | 0.480 |
| TRG_DiLeu_BaEn_4 | 180 | 186 | PF01217 | 0.466 |
| TRG_DiLeu_BaEn_4 | 190 | 196 | PF01217 | 0.485 |
| TRG_DiLeu_BaEn_4 | 220 | 226 | PF01217 | 0.546 |
| TRG_DiLeu_BaEn_4 | 230 | 236 | PF01217 | 0.519 |
| TRG_DiLeu_BaEn_4 | 250 | 256 | PF01217 | 0.543 |
| TRG_DiLeu_BaEn_4 | 260 | 266 | PF01217 | 0.528 |
| TRG_DiLeu_BaEn_4 | 270 | 276 | PF01217 | 0.543 |
| TRG_DiLeu_BaEn_4 | 300 | 306 | PF01217 | 0.561 |
| TRG_DiLeu_BaEn_4 | 310 | 316 | PF01217 | 0.530 |
| TRG_DiLeu_BaEn_4 | 350 | 356 | PF01217 | 0.524 |
| TRG_DiLeu_BaEn_4 | 360 | 366 | PF01217 | 0.491 |
| TRG_DiLeu_BaEn_4 | 370 | 376 | PF01217 | 0.484 |
| TRG_DiLeu_BaEn_4 | 390 | 396 | PF01217 | 0.506 |
| TRG_DiLeu_BaEn_4 | 410 | 416 | PF01217 | 0.500 |
| TRG_DiLeu_BaEn_4 | 420 | 426 | PF01217 | 0.500 |
| TRG_DiLeu_BaEn_4 | 430 | 436 | PF01217 | 0.501 |
| TRG_DiLeu_BaEn_4 | 460 | 466 | PF01217 | 0.543 |
| TRG_DiLeu_BaEn_4 | 470 | 476 | PF01217 | 0.522 |
| TRG_DiLeu_BaEn_4 | 490 | 496 | PF01217 | 0.549 |
| TRG_DiLeu_BaEn_4 | 500 | 506 | PF01217 | 0.564 |
| TRG_DiLeu_BaEn_4 | 510 | 516 | PF01217 | 0.537 |
| TRG_DiLeu_BaEn_4 | 550 | 556 | PF01217 | 0.540 |
| TRG_DiLeu_BaEn_4 | 560 | 566 | PF01217 | 0.506 |
| TRG_DiLeu_BaEn_4 | 570 | 576 | PF01217 | 0.483 |
| TRG_DiLeu_BaEn_4 | 580 | 586 | PF01217 | 0.493 |
| TRG_DiLeu_BaEn_4 | 590 | 596 | PF01217 | 0.493 |
| TRG_DiLeu_BaEn_4 | 60 | 66 | PF01217 | 0.474 |
| TRG_DiLeu_BaEn_4 | 610 | 616 | PF01217 | 0.494 |
| TRG_DiLeu_BaEn_4 | 640 | 646 | PF01217 | 0.486 |
| TRG_DiLeu_BaEn_4 | 690 | 696 | PF01217 | 0.451 |
| TRG_DiLeu_BaEn_4 | 710 | 716 | PF01217 | 0.452 |
| TRG_DiLeu_BaEn_4 | 720 | 726 | PF01217 | 0.451 |
| TRG_DiLeu_BaEn_4 | 80 | 86 | PF01217 | 0.455 |
| TRG_DiLeu_BaEn_4 | 90 | 96 | PF01217 | 0.435 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3Q8IJE1 | Leishmania donovani | 62% | 78% |
| A4HFE2 | Leishmania braziliensis | 88% | 79% |
| A4HFE3 | Leishmania braziliensis | 85% | 100% |
| A4I2L3 | Leishmania infantum | 92% | 100% |