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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AUU2
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 10 |
GO:0051301 | cell division | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 622 | 626 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 651 | 655 | PF00656 | 0.335 |
CLV_C14_Caspase3-7 | 795 | 799 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.536 |
CLV_MEL_PAP_1 | 387 | 393 | PF00089 | 0.586 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 719 | 721 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 718 | 720 | PF00082 | 0.648 |
CLV_PCSK_PC7_1 | 715 | 721 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.315 |
DEG_APCC_DBOX_1 | 259 | 267 | PF00400 | 0.553 |
DEG_SPOP_SBC_1 | 3 | 7 | PF00917 | 0.529 |
DEG_SPOP_SBC_1 | 320 | 324 | PF00917 | 0.672 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.403 |
DEG_SPOP_SBC_1 | 636 | 640 | PF00917 | 0.188 |
DOC_CYCLIN_RxL_1 | 569 | 578 | PF00134 | 0.447 |
DOC_CYCLIN_RxL_1 | 78 | 86 | PF00134 | 0.608 |
DOC_MAPK_gen_1 | 482 | 490 | PF00069 | 0.683 |
DOC_MAPK_gen_1 | 580 | 587 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 683 | 693 | PF00069 | 0.335 |
DOC_MAPK_JIP1_4 | 683 | 689 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 612 | 620 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 683 | 691 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 285 | 292 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.575 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.630 |
DOC_PP2B_LxvP_1 | 545 | 548 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 574 | 577 | PF13499 | 0.447 |
DOC_PP2B_LxvP_1 | 627 | 630 | PF13499 | 0.335 |
DOC_PP2B_PxIxI_1 | 497 | 503 | PF00149 | 0.481 |
DOC_PP4_MxPP_1 | 107 | 110 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 770 | 774 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 757 | 761 | PF12436 | 0.536 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 798 | 803 | PF00397 | 0.747 |
LIG_14-3-3_CanoR_1 | 147 | 153 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 165 | 173 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 644 | 650 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 719 | 726 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 816 | 824 | PF00244 | 0.498 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.445 |
LIG_Clathr_ClatBox_1 | 333 | 337 | PF01394 | 0.362 |
LIG_CSL_BTD_1 | 38 | 41 | PF09270 | 0.560 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.743 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.601 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.584 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.549 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.425 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.526 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.592 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.740 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.585 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.297 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.480 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.636 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.626 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.625 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.684 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.533 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.557 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.447 |
LIG_FHA_2 | 649 | 655 | PF00498 | 0.339 |
LIG_Integrin_RGD_1 | 796 | 798 | PF01839 | 0.651 |
LIG_LIR_Gen_1 | 199 | 208 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 513 | 521 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 95 | 104 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 513 | 518 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.634 |
LIG_MYND_1 | 772 | 776 | PF01753 | 0.665 |
LIG_NRBOX | 246 | 252 | PF00104 | 0.555 |
LIG_NRBOX | 261 | 267 | PF00104 | 0.320 |
LIG_NRBOX | 645 | 651 | PF00104 | 0.335 |
LIG_Rb_pABgroove_1 | 602 | 610 | PF01858 | 0.402 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.593 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.455 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 515 | 519 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 750 | 753 | PF00017 | 0.599 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.534 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.602 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.522 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.668 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.664 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.530 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.587 |
LIG_SH3_3 | 678 | 684 | PF00018 | 0.447 |
LIG_SH3_3 | 766 | 772 | PF00018 | 0.764 |
LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.494 |
LIG_SUMO_SIM_anti_2 | 588 | 594 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 662 | 668 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 736 | 742 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 331 | 338 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 664 | 670 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 735 | 742 | PF11976 | 0.649 |
LIG_WRC_WIRS_1 | 373 | 378 | PF05994 | 0.493 |
LIG_WW_3 | 628 | 632 | PF00397 | 0.335 |
LIG_WW_3 | 768 | 772 | PF00397 | 0.662 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.529 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.685 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.614 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.726 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.335 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.402 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.424 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.660 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.679 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.462 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.472 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.361 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.498 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.447 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.682 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.550 |
MOD_Cter_Amidation | 570 | 573 | PF01082 | 0.402 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.618 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.705 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.628 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.295 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.339 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.366 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.573 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.628 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.635 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.673 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.612 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.555 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.397 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.566 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.537 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.509 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.636 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.682 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.686 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.364 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.445 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.382 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.346 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.624 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.711 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.599 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.418 |
MOD_N-GLC_1 | 752 | 757 | PF02516 | 0.373 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.536 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.576 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.697 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.504 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.549 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.593 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.604 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.387 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.408 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.540 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.585 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.432 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.447 |
MOD_PKA_1 | 467 | 473 | PF00069 | 0.586 |
MOD_PKA_1 | 719 | 725 | PF00069 | 0.722 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.685 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.661 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.378 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.727 |
MOD_PKA_2 | 770 | 776 | PF00069 | 0.644 |
MOD_PKA_2 | 815 | 821 | PF00069 | 0.608 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.385 |
MOD_Plk_1 | 642 | 648 | PF00069 | 0.335 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.622 |
MOD_Plk_2-3 | 293 | 299 | PF00069 | 0.540 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.411 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.530 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.472 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.584 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.355 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.298 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.335 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.662 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.534 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.525 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.560 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.546 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.538 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.695 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.633 |
MOD_ProDKin_1 | 798 | 804 | PF00069 | 0.752 |
MOD_SUMO_for_1 | 756 | 759 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_1 | 742 | 747 | PF01217 | 0.605 |
TRG_DiLeu_BaEn_2 | 52 | 58 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 310 | 315 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 572 | 574 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 630 | 633 | PF00400 | 0.355 |
TRG_NES_CRM1_1 | 530 | 544 | PF08389 | 0.548 |
TRG_NLS_MonoExtC_3 | 717 | 723 | PF00514 | 0.652 |
TRG_NLS_MonoExtN_4 | 715 | 722 | PF00514 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.726 |
TRG_Pf-PMV_PEXEL_1 | 171 | 175 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4E7 | Leptomonas seymouri | 51% | 100% |
A0A1X0NXH5 | Trypanosomatidae | 36% | 100% |
A0A3Q8IBN9 | Leishmania donovani | 90% | 100% |
A0A3R7NWG6 | Trypanosoma rangeli | 37% | 100% |
A4HZ08 | Leishmania infantum | 90% | 100% |
C9ZIP1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AIL0 | Leishmania braziliensis | 75% | 100% |
Q4QCP1 | Leishmania major | 88% | 100% |
V5BCV9 | Trypanosoma cruzi | 34% | 100% |