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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8IG41
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 317 | 321 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.458 |
CLV_MEL_PAP_1 | 552 | 558 | PF00089 | 0.542 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.685 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.753 |
CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.532 |
CLV_PCSK_PC7_1 | 530 | 536 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.780 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.415 |
CLV_Separin_Metazoa | 372 | 376 | PF03568 | 0.409 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.399 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.456 |
DEG_SPOP_SBC_1 | 456 | 460 | PF00917 | 0.512 |
DOC_CDC14_PxL_1 | 23 | 31 | PF14671 | 0.496 |
DOC_CKS1_1 | 489 | 494 | PF01111 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 539 | 545 | PF00134 | 0.708 |
DOC_MAPK_gen_1 | 66 | 72 | PF00069 | 0.513 |
DOC_PP2B_LxvP_1 | 494 | 497 | PF13499 | 0.652 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 681 | 686 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 741 | 746 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 414 | 421 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 447 | 456 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 530 | 534 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 535 | 540 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 692 | 698 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 75 | 80 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 753 | 759 | PF00244 | 0.669 |
LIG_APCC_ABBA_1 | 20 | 25 | PF00400 | 0.533 |
LIG_BRCT_BRCA1_1 | 470 | 474 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 498 | 502 | PF00533 | 0.640 |
LIG_BRCT_BRCA1_1 | 514 | 518 | PF00533 | 0.645 |
LIG_CaM_IQ_9 | 661 | 677 | PF13499 | 0.666 |
LIG_eIF4E_1 | 23 | 29 | PF01652 | 0.511 |
LIG_EVH1_2 | 599 | 603 | PF00568 | 0.715 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.618 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.413 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.522 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.469 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.529 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.459 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.429 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.414 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.260 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.658 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.396 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.803 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.811 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.764 |
LIG_FHA_1 | 742 | 748 | PF00498 | 0.635 |
LIG_FHA_1 | 754 | 760 | PF00498 | 0.596 |
LIG_LIR_Apic_2 | 531 | 536 | PF02991 | 0.731 |
LIG_LIR_Gen_1 | 5 | 15 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 515 | 525 | PF02991 | 0.640 |
LIG_LIR_Gen_1 | 733 | 741 | PF02991 | 0.761 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 515 | 521 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 733 | 737 | PF02991 | 0.767 |
LIG_LIR_Nem_3 | 750 | 755 | PF02991 | 0.571 |
LIG_PCNA_PIPBox_1 | 506 | 515 | PF02747 | 0.699 |
LIG_PTB_Apo_2 | 349 | 356 | PF02174 | 0.490 |
LIG_PTB_Phospho_1 | 349 | 355 | PF10480 | 0.489 |
LIG_SH2_CRK | 657 | 661 | PF00017 | 0.763 |
LIG_SH2_NCK_1 | 405 | 409 | PF00017 | 0.577 |
LIG_SH2_PTP2 | 178 | 181 | PF00017 | 0.481 |
LIG_SH2_SRC | 178 | 181 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 187 | 191 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 657 | 661 | PF00017 | 0.763 |
LIG_SH2_STAP1 | 730 | 734 | PF00017 | 0.769 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.742 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.396 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.546 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.751 |
LIG_SUMO_SIM_anti_2 | 481 | 486 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 25 | 33 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 535 | 541 | PF11976 | 0.800 |
LIG_SUMO_SIM_par_1 | 735 | 740 | PF11976 | 0.686 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.521 |
LIG_TRFH_1 | 8 | 12 | PF08558 | 0.531 |
LIG_TYR_ITIM | 403 | 408 | PF00017 | 0.527 |
MOD_CDC14_SPxK_1 | 296 | 299 | PF00782 | 0.589 |
MOD_CDK_SPxK_1 | 293 | 299 | PF00069 | 0.605 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.705 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.682 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.734 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.579 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.544 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.690 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.602 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.739 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.213 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.546 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.323 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.694 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.745 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.738 |
MOD_Cter_Amidation | 172 | 175 | PF01082 | 0.567 |
MOD_Cter_Amidation | 556 | 559 | PF01082 | 0.673 |
MOD_Cter_Amidation | 64 | 67 | PF01082 | 0.614 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.614 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.767 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.627 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.625 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.555 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.545 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.686 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.654 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.681 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.418 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.544 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.479 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.703 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.738 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.478 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.624 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.688 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.724 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.534 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.569 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.650 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.541 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.663 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.552 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.718 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.585 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.492 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.326 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.630 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.733 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.664 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.790 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.488 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.583 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.585 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.536 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.470 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.656 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.659 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.411 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.664 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.716 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.671 |
MOD_NEK2_2 | 497 | 502 | PF00069 | 0.573 |
MOD_NEK2_2 | 636 | 641 | PF00069 | 0.728 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.602 |
MOD_PIKK_1 | 634 | 640 | PF00454 | 0.787 |
MOD_PK_1 | 142 | 148 | PF00069 | 0.549 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.691 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.769 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.689 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.639 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.760 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.667 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.619 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.730 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.627 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.667 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.467 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.570 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.657 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.667 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.605 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.412 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.667 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.776 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.498 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.321 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.533 |
MOD_Plk_4 | 696 | 702 | PF00069 | 0.601 |
MOD_Plk_4 | 754 | 760 | PF00069 | 0.578 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.662 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.605 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.709 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.711 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.548 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.645 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.745 |
MOD_ProDKin_1 | 681 | 687 | PF00069 | 0.667 |
MOD_ProDKin_1 | 741 | 747 | PF00069 | 0.718 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.709 |
MOD_SUMO_rev_2 | 380 | 389 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 25 | 30 | PF01217 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 24 | 29 | PF01217 | 0.653 |
TRG_DiLeu_BaLyEn_6 | 244 | 249 | PF01217 | 0.678 |
TRG_DiLeu_BaLyEn_6 | 261 | 266 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 465 | 470 | PF01217 | 0.465 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 752 | 755 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 533 | 535 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 606 | 609 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 620 | 623 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 675 | 677 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.684 |
TRG_NLS_MonoCore_2 | 673 | 678 | PF00514 | 0.671 |
TRG_NLS_MonoExtC_3 | 673 | 678 | PF00514 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 288 | 293 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 306 | 310 | PF00026 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKM5 | Leptomonas seymouri | 38% | 99% |
A4HDF3 | Leishmania braziliensis | 73% | 100% |
A4I0T6 | Leishmania infantum | 100% | 100% |
E9AWT8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4QAN6 | Leishmania major | 91% | 100% |