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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3S5H7N2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 172 | 178 | PF00089 | 0.558 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.757 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.765 |
CLV_PCSK_PC1ET2_1 | 423 | 425 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.499 |
DEG_APCC_DBOX_1 | 501 | 509 | PF00400 | 0.428 |
DEG_MDM2_SWIB_1 | 258 | 265 | PF02201 | 0.528 |
DEG_SPOP_SBC_1 | 560 | 564 | PF00917 | 0.368 |
DOC_CYCLIN_RxL_1 | 420 | 428 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 202 | 208 | PF00134 | 0.520 |
DOC_MAPK_RevD_3 | 329 | 344 | PF00069 | 0.572 |
DOC_MIT_MIM_1 | 498 | 508 | PF04212 | 0.511 |
DOC_PP1_RVXF_1 | 326 | 333 | PF00149 | 0.527 |
DOC_PP1_RVXF_1 | 411 | 418 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 247 | 250 | PF13499 | 0.542 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.678 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.633 |
DOC_PP4_FxxP_1 | 417 | 420 | PF00568 | 0.380 |
DOC_SPAK_OSR1_1 | 328 | 332 | PF12202 | 0.442 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.775 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.765 |
LIG_14-3-3_CanoR_1 | 291 | 295 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 424 | 433 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 54 | 62 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.593 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.393 |
LIG_BIR_III_4 | 547 | 551 | PF00653 | 0.402 |
LIG_CaM_NSCaTE_8 | 52 | 59 | PF13499 | 0.484 |
LIG_Clathr_ClatBox_1 | 264 | 268 | PF01394 | 0.430 |
LIG_CSL_BTD_1 | 417 | 420 | PF09270 | 0.414 |
LIG_deltaCOP1_diTrp_1 | 260 | 267 | PF00928 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 456 | 465 | PF00928 | 0.414 |
LIG_eIF4E_1 | 17 | 23 | PF01652 | 0.443 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.590 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.607 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.491 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.413 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.442 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.650 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.376 |
LIG_Integrin_isoDGR_2 | 354 | 356 | PF01839 | 0.699 |
LIG_LIR_Apic_2 | 119 | 125 | PF02991 | 0.680 |
LIG_LIR_Apic_2 | 307 | 312 | PF02991 | 0.637 |
LIG_LIR_Apic_2 | 414 | 420 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 471 | 479 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 497 | 505 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 585 | 593 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 471 | 476 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 585 | 590 | PF02991 | 0.466 |
LIG_NBox_RRM_1 | 267 | 277 | PF00076 | 0.608 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.540 |
LIG_SH2_SRC | 587 | 590 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.432 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.710 |
LIG_SH3_3 | 616 | 622 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 26 | 35 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 561 | 571 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 156 | 163 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 337 | 342 | PF11976 | 0.607 |
LIG_SUMO_SIM_par_1 | 580 | 585 | PF11976 | 0.525 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.588 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.673 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.525 |
LIG_TRAF2_1 | 601 | 604 | PF00917 | 0.529 |
LIG_WW_3 | 123 | 127 | PF00397 | 0.657 |
MOD_CDC14_SPxK_1 | 128 | 131 | PF00782 | 0.648 |
MOD_CDK_SPxK_1 | 125 | 131 | PF00069 | 0.672 |
MOD_CDK_SPxxK_3 | 416 | 423 | PF00069 | 0.435 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.663 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.579 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.469 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.375 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.638 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.626 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.476 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.530 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.562 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.513 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.625 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.607 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.412 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.383 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.524 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.469 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.395 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.553 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.679 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.616 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.526 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.708 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.544 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.511 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.580 |
MOD_GlcNHglycan | 594 | 598 | PF01048 | 0.539 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.756 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.764 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.622 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.653 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.675 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.642 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.669 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.647 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.666 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.565 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.649 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.466 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.574 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.570 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.714 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.402 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.441 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.410 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.541 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.474 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.514 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.612 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.559 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.594 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.746 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.660 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.440 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.438 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.419 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.660 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.543 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.777 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.684 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.657 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.515 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.631 |
MOD_Plk_2-3 | 468 | 474 | PF00069 | 0.482 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.652 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.515 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.474 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.679 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.667 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.530 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.429 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.786 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.466 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.435 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.413 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.761 |
MOD_SUMO_for_1 | 132 | 135 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 466 | 472 | PF00179 | 0.486 |
TRG_DiLeu_BaEn_1 | 135 | 140 | PF01217 | 0.587 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_4 | 280 | 286 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_4 | 450 | 456 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 168 | 173 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 421 | 426 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.492 |
TRG_NES_CRM1_1 | 283 | 295 | PF08389 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 343 | 347 | PF00026 | 0.645 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBM3 | Leptomonas seymouri | 63% | 96% |
A0A1X0P209 | Trypanosomatidae | 33% | 100% |
A4HIE2 | Leishmania braziliensis | 85% | 100% |
A4I5N9 | Leishmania infantum | 100% | 100% |
E9B0Y3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q783 | Leishmania major | 95% | 100% |
V5BL95 | Trypanosoma cruzi | 35% | 100% |