Consists of a solenoid domain with LRR-like helical repeats. Certainly not 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. | no | yes: 0 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HV53
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.446 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.511 |
DEG_APCC_DBOX_1 | 151 | 159 | PF00400 | 0.409 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.472 |
DOC_MAPK_MEF2A_6 | 378 | 387 | PF00069 | 0.407 |
DOC_PP1_RVXF_1 | 159 | 166 | PF00149 | 0.437 |
DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 389 | 392 | PF13499 | 0.385 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.470 |
DOC_USP7_MATH_2 | 468 | 474 | PF00917 | 0.481 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.479 |
LIG_Actin_WH2_2 | 347 | 362 | PF00022 | 0.431 |
LIG_Actin_WH2_2 | 57 | 72 | PF00022 | 0.487 |
LIG_Clathr_ClatBox_1 | 10 | 14 | PF01394 | 0.498 |
LIG_CtBP_PxDLS_1 | 320 | 325 | PF00389 | 0.377 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.505 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.388 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.304 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.474 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.376 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.518 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.650 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.369 |
LIG_LIR_Gen_1 | 12 | 20 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 382 | 392 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 416 | 426 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 472 | 481 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.440 |
LIG_NRBOX | 399 | 405 | PF00104 | 0.392 |
LIG_RPA_C_Fungi | 108 | 120 | PF08784 | 0.314 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 296 | 299 | PF00017 | 0.323 |
LIG_SH2_STAT3 | 92 | 95 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.488 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 189 | 196 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.421 |
LIG_SUMO_SIM_anti_2 | 448 | 454 | PF11976 | 0.384 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.551 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.409 |
LIG_TRFH_1 | 357 | 361 | PF08558 | 0.424 |
LIG_WRC_WIRS_1 | 10 | 15 | PF05994 | 0.576 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.476 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.715 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.386 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.453 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.497 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.624 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.336 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.446 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.545 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.347 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.584 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.671 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.529 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.525 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.303 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.441 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.613 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.358 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.338 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.413 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.338 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.404 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.448 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.544 |
MOD_PK_1 | 242 | 248 | PF00069 | 0.370 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.521 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.501 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.412 |
MOD_Plk_2-3 | 144 | 150 | PF00069 | 0.363 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.446 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.474 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.341 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.390 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.528 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.491 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.462 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.497 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.455 |
MOD_SUMO_for_1 | 37 | 40 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_1 | 396 | 401 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_2 | 352 | 358 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 333 | 338 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKK8 | Leptomonas seymouri | 53% | 99% |
A0A1X0NM47 | Trypanosomatidae | 27% | 100% |
A0A3S5IQL9 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WRW4 | Leishmania donovani | 100% | 100% |
A4H6S5 | Leishmania braziliensis | 82% | 100% |
C9ZQD2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ANT6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QGT4 | Leishmania major | 92% | 100% |
V5BDA8 | Trypanosoma cruzi | 30% | 100% |