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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q1N2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.539 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.534 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.580 |
DOC_CYCLIN_RxL_1 | 297 | 307 | PF00134 | 0.521 |
DOC_CYCLIN_RxL_1 | 319 | 326 | PF00134 | 0.596 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 225 | 234 | PF00069 | 0.559 |
DOC_MAPK_RevD_3 | 132 | 146 | PF00069 | 0.309 |
DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.378 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.560 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.635 |
DOC_USP7_UBL2_3 | 472 | 476 | PF12436 | 0.575 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 22 | 26 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 319 | 325 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.489 |
LIG_Actin_WH2_2 | 7 | 24 | PF00022 | 0.616 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 385 | 389 | PF00533 | 0.543 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.726 |
LIG_CaM_IQ_9 | 348 | 363 | PF13499 | 0.556 |
LIG_eIF4E_1 | 290 | 296 | PF01652 | 0.581 |
LIG_FAT_LD_1 | 175 | 183 | PF03623 | 0.486 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.472 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.562 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.699 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.695 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.496 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.538 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.408 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.491 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.762 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.675 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.621 |
LIG_Integrin_RGD_1 | 220 | 222 | PF01839 | 0.602 |
LIG_LIR_Apic_2 | 159 | 165 | PF02991 | 0.567 |
LIG_LIR_Apic_2 | 422 | 426 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 277 | 287 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 306 | 317 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 386 | 396 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 463 | 471 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.511 |
LIG_LYPXL_yS_3 | 273 | 276 | PF13949 | 0.533 |
LIG_Pex14_1 | 461 | 465 | PF04695 | 0.621 |
LIG_Pex14_2 | 280 | 284 | PF04695 | 0.487 |
LIG_SH2_CRK | 465 | 469 | PF00017 | 0.584 |
LIG_SH2_PTP2 | 423 | 426 | PF00017 | 0.637 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 465 | 469 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.526 |
LIG_SH2_STAT6 | 409 | 413 | PF00017 | 0.579 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.634 |
LIG_SUMO_SIM_par_1 | 331 | 336 | PF11976 | 0.607 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.551 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.577 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.488 |
LIG_UBA3_1 | 178 | 185 | PF00899 | 0.487 |
LIG_UBA3_1 | 53 | 60 | PF00899 | 0.652 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.706 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.575 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.463 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.622 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.534 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.501 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.431 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.428 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.593 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.677 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.620 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.742 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.574 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.692 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.623 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.441 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.612 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.643 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.502 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.762 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.538 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.685 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.523 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.598 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.687 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.658 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.500 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.486 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.620 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.521 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.411 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.417 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.677 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.542 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.530 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.530 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.460 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.602 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.482 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.447 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.520 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.670 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.603 |
MOD_Plk_2-3 | 478 | 484 | PF00069 | 0.614 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.513 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.453 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.539 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.495 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.508 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.624 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.638 |
MOD_SUMO_for_1 | 475 | 478 | PF00179 | 0.579 |
MOD_SUMO_for_1 | 484 | 487 | PF00179 | 0.620 |
MOD_SUMO_rev_2 | 159 | 167 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 226 | 232 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 442 | 450 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 466 | 474 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 64 | 74 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_2 | 113 | 119 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.591 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 123 | 127 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCT1 | Leptomonas seymouri | 61% | 97% |
A0A0S4ITY0 | Bodo saltans | 37% | 100% |
A0A1X0P7R8 | Trypanosomatidae | 30% | 97% |
A0A3S7XAS3 | Leishmania donovani | 92% | 100% |
A0A422MV92 | Trypanosoma rangeli | 30% | 100% |
A4HP57 | Leishmania braziliensis | 74% | 100% |
A4IDG3 | Leishmania infantum | 93% | 100% |
E9ASW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DKS4 | Trypanosoma cruzi | 31% | 100% |