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: Q4QCF0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.396 |
CLV_PCSK_FUR_1 | 235 | 239 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.531 |
CLV_PCSK_PC7_1 | 585 | 591 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.505 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.531 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.420 |
DEG_APCC_DBOX_1 | 497 | 505 | PF00400 | 0.532 |
DEG_APCC_DBOX_1 | 535 | 543 | PF00400 | 0.284 |
DOC_CKS1_1 | 128 | 133 | PF01111 | 0.636 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.468 |
DOC_MAPK_gen_1 | 16 | 24 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 310 | 318 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 536 | 543 | PF00069 | 0.285 |
DOC_MAPK_MEF2A_6 | 79 | 87 | PF00069 | 0.525 |
DOC_MAPK_NFAT4_5 | 536 | 544 | PF00069 | 0.288 |
DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.454 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.483 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.441 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 433 | 440 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 492 | 502 | PF00244 | 0.474 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.366 |
LIG_BRCT_BRCA1_1 | 529 | 533 | PF00533 | 0.507 |
LIG_deltaCOP1_diTrp_1 | 464 | 471 | PF00928 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 576 | 584 | PF00928 | 0.387 |
LIG_eIF4E_1 | 489 | 495 | PF01652 | 0.488 |
LIG_EVH1_1 | 501 | 505 | PF00568 | 0.528 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.518 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.529 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.747 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.591 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.533 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.496 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.378 |
LIG_Integrin_isoDGR_2 | 468 | 470 | PF01839 | 0.341 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 423 | 430 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.446 |
LIG_MAD2 | 417 | 425 | PF02301 | 0.349 |
LIG_MYND_1 | 499 | 503 | PF01753 | 0.563 |
LIG_SH2_CRK | 479 | 483 | PF00017 | 0.507 |
LIG_SH2_NCK_1 | 550 | 554 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.465 |
LIG_SH3_2 | 523 | 528 | PF14604 | 0.608 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.681 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.377 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.522 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.499 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.577 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.661 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.503 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.631 |
LIG_Sin3_3 | 567 | 574 | PF02671 | 0.462 |
LIG_SUMO_SIM_anti_2 | 315 | 320 | PF11976 | 0.528 |
LIG_SUMO_SIM_anti_2 | 537 | 543 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 302 | 307 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 83 | 91 | PF11976 | 0.510 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.552 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.595 |
LIG_TRAF2_1 | 609 | 612 | PF00917 | 0.467 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.342 |
LIG_WW_3 | 554 | 558 | PF00397 | 0.617 |
MOD_CDC14_SPxK_1 | 227 | 230 | PF00782 | 0.521 |
MOD_CDC14_SPxK_1 | 525 | 528 | PF00782 | 0.612 |
MOD_CDC14_SPxK_1 | 554 | 557 | PF00782 | 0.616 |
MOD_CDK_SPxK_1 | 224 | 230 | PF00069 | 0.503 |
MOD_CDK_SPxK_1 | 522 | 528 | PF00069 | 0.609 |
MOD_CDK_SPxK_1 | 551 | 557 | PF00069 | 0.634 |
MOD_CDK_SPxxK_3 | 224 | 231 | PF00069 | 0.507 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.718 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.407 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.479 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.516 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.391 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.523 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.475 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.530 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.627 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.584 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.388 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.430 |
MOD_CMANNOS | 146 | 149 | PF00535 | 0.435 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.466 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.723 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.438 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.656 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.592 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.604 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.524 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.571 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.574 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.576 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.638 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.624 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.581 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.681 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.550 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.595 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.594 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.581 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.486 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.690 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.589 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.637 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.621 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.515 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.443 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.497 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.633 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.427 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.413 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.511 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.436 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.389 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.509 |
MOD_PKA_1 | 230 | 236 | PF00069 | 0.608 |
MOD_PKA_1 | 589 | 595 | PF00069 | 0.395 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.608 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.415 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.445 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.496 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.400 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.417 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.564 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.574 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.553 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.666 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.495 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.347 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.555 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.463 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.530 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.492 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.673 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.477 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.459 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.563 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.396 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.609 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.634 |
TRG_DiLeu_BaEn_4 | 257 | 263 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 588 | 590 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 603 | 605 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 628 | 631 | PF00400 | 0.400 |
TRG_NES_CRM1_1 | 442 | 455 | PF08389 | 0.504 |
TRG_NLS_Bipartite_1 | 230 | 251 | PF00514 | 0.585 |
TRG_NLS_MonoExtN_4 | 244 | 251 | PF00514 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 310 | 315 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAU6 | Leptomonas seymouri | 50% | 100% |
A0A1X0NYZ1 | Trypanosomatidae | 24% | 100% |
A0A3Q8IBW5 | Leishmania donovani | 94% | 100% |
A0A422NHB0 | Trypanosoma rangeli | 25% | 100% |
A4HBR2 | Leishmania braziliensis | 77% | 100% |
A4HZ64 | Leishmania infantum | 94% | 80% |
D0A1H9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AV31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BIF6 | Trypanosoma cruzi | 25% | 100% |