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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9ALY7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.239 |
DEG_APCC_DBOX_1 | 66 | 74 | PF00400 | 0.396 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.573 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.551 |
DEG_SCF_FBW7_1 | 363 | 369 | PF00400 | 0.531 |
DEG_SPOP_SBC_1 | 366 | 370 | PF00917 | 0.615 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.572 |
DOC_CYCLIN_RxL_1 | 405 | 415 | PF00134 | 0.375 |
DOC_CYCLIN_RxL_1 | 447 | 456 | PF00134 | 0.346 |
DOC_CYCLIN_RxL_1 | 457 | 466 | PF00134 | 0.370 |
DOC_MAPK_gen_1 | 455 | 464 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 97 | 105 | PF00069 | 0.328 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.386 |
DOC_USP7_UBL2_3 | 343 | 347 | PF12436 | 0.566 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.484 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 477 | 483 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 1 | 18 | PF00022 | 0.524 |
LIG_AP2alpha_1 | 277 | 281 | PF02296 | 0.413 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.587 |
LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.202 |
LIG_CaM_IQ_9 | 242 | 257 | PF13499 | 0.420 |
LIG_CaM_NSCaTE_8 | 152 | 159 | PF13499 | 0.445 |
LIG_eIF4E_1 | 447 | 453 | PF01652 | 0.388 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.407 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.473 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.448 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.508 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.393 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.362 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.497 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.410 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.340 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.602 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.497 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.412 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.533 |
LIG_GBD_Chelix_1 | 403 | 411 | PF00786 | 0.467 |
LIG_LIR_Gen_1 | 169 | 178 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 202 | 212 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.196 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.395 |
LIG_LRP6_Inhibitor_1 | 24 | 30 | PF00058 | 0.481 |
LIG_NRBOX | 337 | 343 | PF00104 | 0.493 |
LIG_PCNA_yPIPBox_3 | 26 | 40 | PF02747 | 0.525 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.413 |
LIG_SH2_STAT3 | 413 | 416 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.385 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.569 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.480 |
LIG_TRAF2_1 | 257 | 260 | PF00917 | 0.412 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.339 |
LIG_UBA3_1 | 111 | 115 | PF00899 | 0.393 |
MOD_CDK_SPxxK_3 | 483 | 490 | PF00069 | 0.635 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.461 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.341 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.586 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.414 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.466 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.299 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.479 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.435 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.400 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.342 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.554 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.460 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.597 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.508 |
MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.388 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.528 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.542 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.524 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.475 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.526 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.425 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.477 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.509 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.446 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.502 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.483 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.476 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.510 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.489 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.470 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.356 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.533 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.457 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.311 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.449 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.537 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.407 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.554 |
MOD_NEK2_2 | 159 | 164 | PF00069 | 0.434 |
MOD_NEK2_2 | 377 | 382 | PF00069 | 0.627 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.475 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.366 |
MOD_PK_1 | 347 | 353 | PF00069 | 0.519 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.568 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.471 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.301 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.461 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.437 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.568 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.511 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.465 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.623 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.390 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.425 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.537 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.610 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.475 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 219 | 222 | PF00179 | 0.513 |
MOD_SUMO_for_1 | 314 | 317 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 107 | 117 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 135 | 144 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 177 | 182 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 333 | 338 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 469 | 475 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_4 | 259 | 265 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 470 | 474 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9E1 | Leptomonas seymouri | 80% | 100% |
A0A0S4IX38 | Bodo saltans | 29% | 95% |
A0A1X0P156 | Trypanosomatidae | 45% | 100% |
A0A3S7X2A6 | Leishmania donovani | 96% | 100% |
A0A422NRS1 | Trypanosoma rangeli | 44% | 100% |
A4HH97 | Leishmania braziliensis | 87% | 100% |
A4I4E3 | Leishmania infantum | 96% | 100% |
C9ZL20 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9ADU3 | Leishmania major | 95% | 100% |
V5BR79 | Trypanosoma cruzi | 45% | 100% |