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: A4IA08
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.589 |
CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 690 | 694 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.718 |
CLV_PCSK_FUR_1 | 512 | 516 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.650 |
CLV_PCSK_PC7_1 | 297 | 303 | PF00082 | 0.639 |
CLV_PCSK_PC7_1 | 669 | 675 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.719 |
CLV_Separin_Metazoa | 106 | 110 | PF03568 | 0.513 |
CLV_Separin_Metazoa | 491 | 495 | PF03568 | 0.507 |
DEG_COP1_1 | 7 | 16 | PF00400 | 0.587 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.603 |
DEG_SPOP_SBC_1 | 590 | 594 | PF00917 | 0.756 |
DEG_SPOP_SBC_1 | 655 | 659 | PF00917 | 0.710 |
DOC_CKS1_1 | 613 | 618 | PF01111 | 0.475 |
DOC_CYCLIN_RxL_1 | 398 | 407 | PF00134 | 0.435 |
DOC_CYCLIN_RxL_1 | 497 | 507 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 672 | 678 | PF00134 | 0.626 |
DOC_MAPK_MEF2A_6 | 109 | 118 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 355 | 362 | PF00069 | 0.439 |
DOC_PP1_RVXF_1 | 400 | 406 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 606 | 609 | PF00568 | 0.674 |
DOC_PP4_FxxP_1 | 613 | 616 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.749 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.249 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 707 | 712 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.741 |
LIG_14-3-3_CanoR_1 | 201 | 211 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 216 | 222 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 402 | 410 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 47 | 57 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 93 | 111 | PF00022 | 0.516 |
LIG_BIR_III_2 | 52 | 56 | PF00653 | 0.643 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_1 | 591 | 595 | PF00533 | 0.748 |
LIG_deltaCOP1_diTrp_1 | 197 | 202 | PF00928 | 0.376 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.673 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.478 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.507 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.570 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.486 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.522 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.566 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.719 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.779 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.736 |
LIG_Integrin_RGD_1 | 582 | 584 | PF01839 | 0.716 |
LIG_IRF3_LxIS_1 | 310 | 316 | PF10401 | 0.573 |
LIG_LIR_Apic_2 | 612 | 616 | PF02991 | 0.547 |
LIG_LIR_Apic_2 | 627 | 632 | PF02991 | 0.429 |
LIG_LIR_Apic_2 | 9 | 14 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.552 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.541 |
LIG_NRBOX | 93 | 99 | PF00104 | 0.574 |
LIG_PCNA_yPIPBox_3 | 137 | 148 | PF02747 | 0.566 |
LIG_PCNA_yPIPBox_3 | 391 | 404 | PF02747 | 0.568 |
LIG_PDZ_Class_3 | 745 | 750 | PF00595 | 0.664 |
LIG_Pex14_2 | 118 | 122 | PF04695 | 0.409 |
LIG_SH2_SRC | 662 | 665 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 548 | 551 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.587 |
LIG_SH3_1 | 629 | 635 | PF00018 | 0.476 |
LIG_SH3_2 | 266 | 271 | PF14604 | 0.607 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.606 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.655 |
LIG_SH3_3 | 629 | 635 | PF00018 | 0.586 |
LIG_Sin3_3 | 430 | 437 | PF02671 | 0.468 |
LIG_SUMO_SIM_anti_2 | 450 | 455 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 145 | 152 | PF11976 | 0.604 |
LIG_SUMO_SIM_par_1 | 309 | 314 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 586 | 594 | PF11976 | 0.749 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.508 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.521 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.760 |
MOD_CDC14_SPxK_1 | 235 | 238 | PF00782 | 0.672 |
MOD_CDC14_SPxK_1 | 268 | 271 | PF00782 | 0.604 |
MOD_CDC14_SPxK_1 | 298 | 301 | PF00782 | 0.741 |
MOD_CDC14_SPxK_1 | 44 | 47 | PF00782 | 0.654 |
MOD_CDC14_SPxK_1 | 579 | 582 | PF00782 | 0.770 |
MOD_CDK_SPxK_1 | 232 | 238 | PF00069 | 0.681 |
MOD_CDK_SPxK_1 | 265 | 271 | PF00069 | 0.608 |
MOD_CDK_SPxK_1 | 295 | 301 | PF00069 | 0.756 |
MOD_CDK_SPxK_1 | 41 | 47 | PF00069 | 0.668 |
MOD_CDK_SPxK_1 | 576 | 582 | PF00069 | 0.770 |
MOD_CDK_SPxxK_3 | 295 | 302 | PF00069 | 0.751 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.484 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.591 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.648 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.315 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.493 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.746 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.654 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.722 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.622 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.751 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.733 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.818 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.719 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.557 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.559 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.554 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.515 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.713 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.747 |
MOD_CK2_1 | 718 | 724 | PF00069 | 0.788 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.550 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.555 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.486 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.528 |
MOD_GlcNHglycan | 286 | 290 | PF01048 | 0.642 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.592 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.413 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.548 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.541 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.472 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.712 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.591 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.743 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.715 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.769 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.723 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.830 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.766 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.687 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.503 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.572 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.570 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.577 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.668 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.304 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.568 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.765 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.725 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.750 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.792 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.762 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.698 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.765 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.639 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.609 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.511 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.706 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.451 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.437 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.454 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.407 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.567 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.578 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.693 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.755 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.554 |
MOD_NEK2_2 | 274 | 279 | PF00069 | 0.561 |
MOD_NEK2_2 | 384 | 389 | PF00069 | 0.592 |
MOD_NEK2_2 | 569 | 574 | PF00069 | 0.581 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.595 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.633 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.556 |
MOD_PIKK_1 | 547 | 553 | PF00454 | 0.702 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.435 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.714 |
MOD_PKA_2 | 716 | 722 | PF00069 | 0.738 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.668 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.439 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.757 |
MOD_Plk_1 | 684 | 690 | PF00069 | 0.735 |
MOD_Plk_1 | 731 | 737 | PF00069 | 0.597 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.550 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.493 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.452 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.557 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.751 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.757 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.763 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.751 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.591 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.577 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.492 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.681 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.584 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.749 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.255 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.692 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.744 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.451 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.573 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.785 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.667 |
MOD_ProDKin_1 | 707 | 713 | PF00069 | 0.544 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.738 |
TRG_DiLeu_BaEn_1 | 633 | 638 | PF01217 | 0.688 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 511 | 514 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 672 | 674 | PF00400 | 0.788 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8V5 | Leptomonas seymouri | 59% | 99% |
A0A1X0PAK4 | Trypanosomatidae | 31% | 100% |
A0A3R7N1B1 | Trypanosoma rangeli | 33% | 100% |
A0A3S7X7X6 | Leishmania donovani | 100% | 100% |
A4HAU0 | Leishmania braziliensis | 73% | 100% |
E9B514 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
Q4Q2X2 | Leishmania major | 92% | 100% |