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. | yes | yes: 20 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 9 |
GO:0042995 | cell projection | 2 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 9 |
Related structures:
AlphaFold database: E9B018
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 9 |
GO:0008047 | enzyme activator activity | 3 | 9 |
GO:0030234 | enzyme regulator activity | 2 | 9 |
GO:0030695 | GTPase regulator activity | 4 | 9 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 9 |
GO:0098772 | molecular function regulator activity | 1 | 9 |
GO:0140677 | molecular function activator activity | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.789 |
CLV_C14_Caspase3-7 | 642 | 646 | PF00656 | 0.597 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.852 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.792 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.654 |
CLV_PCSK_FUR_1 | 461 | 465 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.852 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 377 | 383 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.647 |
CLV_Separin_Metazoa | 228 | 232 | PF03568 | 0.422 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.605 |
DEG_Kelch_Keap1_1 | 707 | 712 | PF01344 | 0.736 |
DEG_SCF_FBW7_1 | 233 | 239 | PF00400 | 0.488 |
DOC_ANK_TNKS_1 | 400 | 407 | PF00023 | 0.704 |
DOC_CDC14_PxL_1 | 177 | 185 | PF14671 | 0.398 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.489 |
DOC_CKS1_1 | 485 | 490 | PF01111 | 0.681 |
DOC_CKS1_1 | 529 | 534 | PF01111 | 0.645 |
DOC_CYCLIN_RxL_1 | 66 | 77 | PF00134 | 0.460 |
DOC_MAPK_DCC_7 | 350 | 358 | PF00069 | 0.637 |
DOC_MAPK_gen_1 | 350 | 358 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 553 | 561 | PF00069 | 0.569 |
DOC_PP2B_LxvP_1 | 741 | 744 | PF13499 | 0.664 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.527 |
DOC_USP7_UBL2_3 | 542 | 546 | PF12436 | 0.569 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.731 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 444 | 450 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 486 | 492 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 689 | 693 | PF00244 | 0.774 |
LIG_14-3-3_CanoR_1 | 746 | 750 | PF00244 | 0.710 |
LIG_APCC_ABBA_1 | 255 | 260 | PF00400 | 0.386 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.584 |
LIG_BIR_III_4 | 645 | 649 | PF00653 | 0.655 |
LIG_BRCT_BRCA1_1 | 749 | 753 | PF00533 | 0.712 |
LIG_Clathr_ClatBox_1 | 296 | 300 | PF01394 | 0.475 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.395 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.475 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.492 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.353 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.342 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.581 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.587 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.520 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.577 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.575 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.452 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.820 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.775 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.700 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.640 |
LIG_FHA_2 | 562 | 568 | PF00498 | 0.587 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.488 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.695 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.798 |
LIG_IRF3_LxIS_1 | 7 | 14 | PF10401 | 0.307 |
LIG_LIR_Apic_2 | 334 | 338 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 75 | 81 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 623 | 632 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 623 | 628 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 649 | 655 | PF02991 | 0.629 |
LIG_LRP6_Inhibitor_1 | 92 | 98 | PF00058 | 0.446 |
LIG_PCNA_yPIPBox_3 | 321 | 329 | PF02747 | 0.542 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.333 |
LIG_SH2_CRK | 625 | 629 | PF00017 | 0.686 |
LIG_SH2_CRK | 637 | 641 | PF00017 | 0.606 |
LIG_SH2_NCK_1 | 375 | 379 | PF00017 | 0.636 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 172 | 175 | PF00017 | 0.392 |
LIG_SH2_STAT3 | 655 | 658 | PF00017 | 0.713 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.589 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.684 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 295 | 300 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 311 | 316 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 518 | 527 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 127 | 133 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 154 | 159 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 212 | 217 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 69 | 75 | PF11976 | 0.453 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.550 |
LIG_TRAF2_1 | 437 | 440 | PF00917 | 0.719 |
LIG_TYR_ITIM | 188 | 193 | PF00017 | 0.333 |
LIG_TYR_ITIM | 635 | 640 | PF00017 | 0.658 |
LIG_UBA3_1 | 297 | 305 | PF00899 | 0.400 |
LIG_UBA3_1 | 540 | 546 | PF00899 | 0.463 |
MOD_CDC14_SPxK_1 | 590 | 593 | PF00782 | 0.776 |
MOD_CDK_SPK_2 | 446 | 451 | PF00069 | 0.734 |
MOD_CDK_SPK_2 | 456 | 461 | PF00069 | 0.596 |
MOD_CDK_SPK_2 | 484 | 489 | PF00069 | 0.695 |
MOD_CDK_SPxK_1 | 587 | 593 | PF00069 | 0.773 |
MOD_CDK_SPxxK_3 | 456 | 463 | PF00069 | 0.589 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.723 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.689 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.711 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.799 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.740 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.775 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.729 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.451 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.592 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.735 |
MOD_DYRK1A_RPxSP_1 | 432 | 436 | PF00069 | 0.686 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.468 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.454 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.435 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.875 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.664 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.710 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.754 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.727 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.803 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.699 |
MOD_GlcNHglycan | 708 | 712 | PF01048 | 0.822 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.609 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.365 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.436 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.483 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.589 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.636 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.630 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.792 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.596 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.736 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.656 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.768 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.486 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.695 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.701 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.742 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.716 |
MOD_LATS_1 | 452 | 458 | PF00433 | 0.703 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.514 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.430 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.340 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.497 |
MOD_N-GLC_1 | 664 | 669 | PF02516 | 0.632 |
MOD_N-GLC_2 | 681 | 683 | PF02516 | 0.544 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.547 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.448 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.390 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.656 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.727 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.649 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.750 |
MOD_NEK2_2 | 368 | 373 | PF00069 | 0.549 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.791 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.533 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.784 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.450 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.605 |
MOD_PIKK_1 | 676 | 682 | PF00454 | 0.706 |
MOD_PIKK_1 | 693 | 699 | PF00454 | 0.718 |
MOD_PK_1 | 425 | 431 | PF00069 | 0.678 |
MOD_PKA_1 | 373 | 379 | PF00069 | 0.578 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.598 |
MOD_PKA_1 | 454 | 460 | PF00069 | 0.703 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.514 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.587 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.634 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.794 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.798 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.852 |
MOD_PKA_2 | 676 | 682 | PF00069 | 0.730 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.783 |
MOD_PKA_2 | 745 | 751 | PF00069 | 0.712 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.383 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.391 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.351 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.636 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.449 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.469 |
MOD_Plk_2-3 | 522 | 528 | PF00069 | 0.564 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.398 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.524 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.348 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.407 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.596 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.511 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.503 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.729 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.711 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.743 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.789 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.640 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.787 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.716 |
MOD_ProDKin_1 | 733 | 739 | PF00069 | 0.731 |
MOD_SUMO_rev_2 | 32 | 38 | PF00179 | 0.620 |
TRG_DiLeu_BaEn_4 | 348 | 354 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.720 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.720 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.717 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 69 | 74 | PF00026 | 0.316 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NQV7 | Trypanosomatidae | 43% | 100% |
A0A3Q8II72 | Leishmania donovani | 93% | 100% |
A0A422NBD9 | Trypanosoma rangeli | 43% | 100% |
A4HGP9 | Leishmania braziliensis | 74% | 100% |
A4I3S6 | Leishmania infantum | 93% | 100% |
D0A881 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
Q4Q867 | Leishmania major | 91% | 99% |