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 |
Related structures:
AlphaFold database: Q4Q8S6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.570 |
DEG_APCC_DBOX_1 | 546 | 554 | PF00400 | 0.465 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.435 |
DEG_COP1_1 | 272 | 281 | PF00400 | 0.487 |
DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.534 |
DOC_CKS1_1 | 273 | 278 | PF01111 | 0.485 |
DOC_CKS1_1 | 540 | 545 | PF01111 | 0.645 |
DOC_MAPK_gen_1 | 475 | 484 | PF00069 | 0.667 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.685 |
DOC_MAPK_MEF2A_6 | 68 | 75 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 77 | 84 | PF00069 | 0.485 |
DOC_PP1_RVXF_1 | 565 | 571 | PF00149 | 0.389 |
DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.655 |
DOC_PP4_FxxP_1 | 382 | 385 | PF00568 | 0.362 |
DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.332 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.691 |
DOC_USP7_MATH_2 | 543 | 549 | PF00917 | 0.461 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 211 | 216 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 234 | 238 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 312 | 319 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 440 | 449 | PF00244 | 0.654 |
LIG_Actin_WH2_2 | 90 | 108 | PF00022 | 0.431 |
LIG_APCC_ABBA_1 | 459 | 464 | PF00400 | 0.505 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.660 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.588 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.710 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.705 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.398 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.625 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.537 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.521 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.336 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.786 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.706 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.674 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.436 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.453 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.602 |
LIG_FXI_DFP_1 | 217 | 221 | PF00024 | 0.509 |
LIG_GBD_Chelix_1 | 38 | 46 | PF00786 | 0.511 |
LIG_Integrin_isoDGR_2 | 209 | 211 | PF01839 | 0.561 |
LIG_IRF3_LxIS_1 | 74 | 81 | PF10401 | 0.497 |
LIG_LIR_Apic_2 | 191 | 197 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 381 | 385 | PF02991 | 0.361 |
LIG_LIR_Apic_2 | 530 | 534 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 538 | 543 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 214 | 225 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.455 |
LIG_LYPXL_yS_3 | 507 | 510 | PF13949 | 0.376 |
LIG_LYPXL_yS_3 | 578 | 581 | PF13949 | 0.433 |
LIG_SH2_NCK_1 | 540 | 544 | PF00017 | 0.552 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.284 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.810 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.591 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.523 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.646 |
LIG_SUMO_SIM_anti_2 | 69 | 75 | PF11976 | 0.418 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.480 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.598 |
LIG_TRAF2_1 | 542 | 545 | PF00917 | 0.449 |
LIG_UBA3_1 | 479 | 485 | PF00899 | 0.577 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.496 |
MOD_CDK_SPxxK_3 | 305 | 312 | PF00069 | 0.609 |
MOD_CDK_SPxxK_3 | 539 | 546 | PF00069 | 0.459 |
MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.588 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.705 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.718 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.630 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.488 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.654 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.468 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.409 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.571 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.669 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.548 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.643 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.493 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.637 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.391 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.410 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.493 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.644 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.452 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.565 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.693 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.438 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.594 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.367 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.581 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.500 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.568 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.484 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.605 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.722 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.592 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.641 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.584 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.501 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.522 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.365 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.481 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.476 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.511 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.495 |
MOD_N-GLC_2 | 118 | 120 | PF02516 | 0.624 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.390 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.445 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.555 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.499 |
MOD_NEK2_2 | 465 | 470 | PF00069 | 0.488 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.643 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.609 |
MOD_PK_1 | 158 | 164 | PF00069 | 0.561 |
MOD_PK_1 | 429 | 435 | PF00069 | 0.494 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.604 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.451 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.652 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.753 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.751 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.589 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.582 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.664 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.614 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.442 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.589 |
MOD_Plk_2-3 | 354 | 360 | PF00069 | 0.504 |
MOD_Plk_2-3 | 506 | 512 | PF00069 | 0.520 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.553 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.605 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.694 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.435 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.508 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.551 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.733 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.486 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.566 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.543 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.457 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.643 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.633 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.475 |
MOD_SUMO_rev_2 | 185 | 195 | PF00179 | 0.374 |
MOD_SUMO_rev_2 | 511 | 519 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 9 | 15 | PF00179 | 0.627 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_1 | 70 | 75 | PF01217 | 0.467 |
TRG_DiLeu_LyEn_5 | 409 | 414 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 440 | 444 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I848 | Leptomonas seymouri | 56% | 100% |
A0A1X0P7D0 | Trypanosomatidae | 32% | 100% |
A0A3R7MCE3 | Trypanosoma rangeli | 35% | 100% |
A0A3S7X099 | Leishmania donovani | 94% | 100% |
A4HFA9 | Leishmania braziliensis | 79% | 100% |
A4I2J1 | Leishmania infantum | 94% | 100% |
C9ZWZ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AYP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5B7P2 | Trypanosoma cruzi | 34% | 100% |