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: 3 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: Q4QBG8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 30 | 36 | PF00089 | 0.435 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 254 | 256 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.369 |
DOC_CYCLIN_RxL_1 | 124 | 131 | PF00134 | 0.442 |
DOC_MAPK_gen_1 | 229 | 237 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 399 | 407 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 52 | 62 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 273 | 282 | PF00069 | 0.424 |
DOC_MAPK_NFAT4_5 | 273 | 281 | PF00069 | 0.435 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.472 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 170 | 179 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 273 | 279 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 282 | 299 | PF00022 | 0.593 |
LIG_Actin_WH2_2 | 87 | 102 | PF00022 | 0.353 |
LIG_APCC_ABBA_1 | 321 | 326 | PF00400 | 0.368 |
LIG_APCC_ABBAyCdc20_2 | 254 | 260 | PF00400 | 0.484 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.588 |
LIG_CtBP_PxDLS_1 | 81 | 85 | PF00389 | 0.502 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.586 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.435 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.518 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.533 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.572 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.447 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.447 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.579 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.625 |
LIG_SH2_CRK | 244 | 248 | PF00017 | 0.472 |
LIG_SH2_GRB2like | 388 | 391 | PF00017 | 0.378 |
LIG_SH2_SRC | 388 | 391 | PF00017 | 0.378 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.640 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 318 | 326 | PF11976 | 0.378 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.434 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.623 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.590 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.398 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.401 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.445 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.436 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.464 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.572 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.630 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.625 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.446 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.301 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.512 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.483 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.601 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.526 |
MOD_GlcNHglycan | 325 | 330 | PF01048 | 0.563 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.437 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.630 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.589 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.559 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.585 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.534 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.411 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.439 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.411 |
MOD_LATS_1 | 391 | 397 | PF00433 | 0.464 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.433 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.382 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.462 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.471 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.561 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.563 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.514 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.580 |
MOD_PKA_1 | 133 | 139 | PF00069 | 0.619 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.566 |
MOD_PKA_1 | 393 | 399 | PF00069 | 0.525 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.622 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.677 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.434 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.454 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.414 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.421 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.500 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.580 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.601 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.478 |
MOD_Plk_2-3 | 168 | 174 | PF00069 | 0.494 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.512 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.387 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.421 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.532 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.562 |
MOD_SUMO_for_1 | 44 | 47 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 126 | 135 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 152 | 161 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 343 | 352 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 353 | 360 | PF00179 | 0.406 |
TRG_DiLeu_BaEn_1 | 157 | 162 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.438 |
TRG_DiLeu_BaEn_4 | 46 | 52 | PF01217 | 0.436 |
TRG_DiLeu_LyEn_5 | 157 | 162 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.459 |
TRG_NES_CRM1_1 | 53 | 66 | PF08389 | 0.444 |
TRG_NES_CRM1_1 | 68 | 82 | PF08389 | 0.508 |
TRG_NES_CRM1_1 | 86 | 97 | PF08389 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 248 | 253 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 255 | 260 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.657 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HV61 | Leptomonas seymouri | 71% | 100% |
A0A0S4J5N8 | Bodo saltans | 37% | 96% |
A0A1X0NXM5 | Trypanosomatidae | 45% | 100% |
A0A3S7WXH9 | Leishmania donovani | 94% | 100% |
A0A422N5Q1 | Trypanosoma rangeli | 45% | 99% |
A4HCM1 | Leishmania braziliensis | 78% | 100% |
A4I045 | Leishmania infantum | 94% | 100% |
C9ZUY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AW08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5B6S0 | Trypanosoma cruzi | 47% | 84% |