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: A4HBR2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.472 |
CLV_PCSK_FUR_1 | 235 | 239 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.586 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.560 |
DEG_APCC_DBOX_1 | 497 | 505 | PF00400 | 0.653 |
DOC_CKS1_1 | 159 | 164 | PF01111 | 0.552 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.624 |
DOC_MAPK_gen_1 | 16 | 24 | PF00069 | 0.432 |
DOC_MAPK_JIP1_4 | 498 | 504 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 311 | 318 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 452 | 460 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.493 |
DOC_PP2B_LxvP_1 | 502 | 505 | PF13499 | 0.466 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.521 |
DOC_PP2B_PxIxI_1 | 32 | 38 | PF00149 | 0.462 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.594 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.638 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 264 | 272 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 384 | 394 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 428 | 437 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 492 | 502 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 79 | 87 | PF00244 | 0.464 |
LIG_APCC_ABBA_1 | 581 | 586 | PF00400 | 0.301 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.425 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.388 |
LIG_deltaCOP1_diTrp_1 | 464 | 471 | PF00928 | 0.491 |
LIG_eIF4E_1 | 489 | 495 | PF01652 | 0.527 |
LIG_EVH1_1 | 159 | 163 | PF00568 | 0.420 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.676 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.538 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.584 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.509 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.755 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.658 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.553 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.660 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.344 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.295 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.460 |
LIG_LIR_Apic_2 | 105 | 111 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.472 |
LIG_MYND_1 | 499 | 503 | PF01753 | 0.708 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.574 |
LIG_SH2_CRK | 479 | 483 | PF00017 | 0.558 |
LIG_SH2_NCK_1 | 550 | 554 | PF00017 | 0.711 |
LIG_SH2_SRC | 550 | 553 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.642 |
LIG_SH3_2 | 523 | 528 | PF14604 | 0.743 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.514 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.756 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.632 |
LIG_Sin3_3 | 567 | 574 | PF02671 | 0.508 |
LIG_SUMO_SIM_anti_2 | 315 | 320 | PF11976 | 0.598 |
LIG_SUMO_SIM_anti_2 | 436 | 441 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 73 | 78 | PF11976 | 0.304 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.611 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.671 |
LIG_TRAF2_1 | 609 | 612 | PF00917 | 0.609 |
LIG_UBA3_1 | 96 | 100 | PF00899 | 0.306 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.404 |
LIG_WRC_WIRS_1 | 92 | 97 | PF05994 | 0.498 |
LIG_WW_3 | 554 | 558 | PF00397 | 0.644 |
MOD_CDC14_SPxK_1 | 525 | 528 | PF00782 | 0.710 |
MOD_CDC14_SPxK_1 | 554 | 557 | PF00782 | 0.657 |
MOD_CDK_SPxK_1 | 522 | 528 | PF00069 | 0.728 |
MOD_CDK_SPxK_1 | 551 | 557 | PF00069 | 0.673 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.593 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.673 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.468 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.522 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.565 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.565 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.467 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.512 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.580 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.532 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.496 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.636 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.558 |
MOD_CMANNOS | 146 | 149 | PF00535 | 0.505 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.529 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.630 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.489 |
MOD_GlcNHglycan | 202 | 206 | PF01048 | 0.685 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.615 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.594 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.613 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.680 |
MOD_GlcNHglycan | 383 | 387 | PF01048 | 0.676 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.562 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.489 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.390 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.509 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.578 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.723 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.656 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.636 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.505 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.643 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.600 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.726 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.543 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.667 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.422 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.468 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.763 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.509 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.546 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.539 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.499 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.438 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.548 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.564 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.632 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.536 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.568 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.465 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.624 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.585 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.567 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.485 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.371 |
MOD_PKA_1 | 230 | 236 | PF00069 | 0.622 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.371 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.621 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.385 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.491 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.588 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.479 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.513 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.610 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.661 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.579 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.587 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.568 |
MOD_Plk_2-3 | 239 | 245 | PF00069 | 0.409 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.715 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.721 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.694 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.383 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.638 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.568 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.621 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.385 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.383 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.508 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.501 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.548 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.751 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.457 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.460 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.616 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.396 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.728 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.635 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.594 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.713 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.543 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 603 | 605 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 628 | 631 | PF00400 | 0.474 |
TRG_NLS_Bipartite_1 | 230 | 251 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 244 | 251 | PF00514 | 0.671 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAU6 | Leptomonas seymouri | 50% | 100% |
A0A1X0NYZ1 | Trypanosomatidae | 24% | 100% |
A0A3Q8IBW5 | Leishmania donovani | 77% | 100% |
A0A422NHB0 | Trypanosoma rangeli | 25% | 100% |
A4HZ64 | Leishmania infantum | 77% | 80% |
D0A1H9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AV31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QCF0 | Leishmania major | 77% | 100% |
V5BIF6 | Trypanosoma cruzi | 24% | 100% |