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: 40 |
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 2 |
GO:0005875 | microtubule associated complex | 2 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0051286 | cell tip | 3 | 2 |
GO:0060187 | cell pole | 2 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0099081 | supramolecular polymer | 3 | 2 |
GO:0099512 | supramolecular fiber | 4 | 2 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0035869 | ciliary transition zone | 2 | 1 |
Related structures:
AlphaFold database: A4H4R6
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 16 |
GO:0007018 | microtubule-based movement | 3 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0051231 | spindle elongation | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003774 | cytoskeletal motor activity | 1 | 16 |
GO:0003777 | microtubule motor activity | 2 | 16 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 16 |
GO:0005515 | protein binding | 2 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0008017 | microtubule binding | 5 | 16 |
GO:0008092 | cytoskeletal protein binding | 3 | 16 |
GO:0015631 | tubulin binding | 4 | 16 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.202 |
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.202 |
CLV_C14_Caspase3-7 | 553 | 557 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 559 | 563 | PF00656 | 0.470 |
CLV_C14_Caspase3-7 | 574 | 578 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 625 | 629 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 763 | 767 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 816 | 818 | PF00675 | 0.600 |
CLV_PCSK_FUR_1 | 388 | 392 | PF00082 | 0.505 |
CLV_PCSK_FUR_1 | 814 | 818 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 816 | 818 | PF00082 | 0.600 |
CLV_PCSK_PC7_1 | 227 | 233 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.459 |
CLV_Separin_Metazoa | 838 | 842 | PF03568 | 0.429 |
DEG_APCC_DBOX_1 | 178 | 186 | PF00400 | 0.202 |
DEG_APCC_DBOX_1 | 505 | 513 | PF00400 | 0.393 |
DEG_APCC_DBOX_1 | 870 | 878 | PF00400 | 0.422 |
DOC_ANK_TNKS_1 | 572 | 579 | PF00023 | 0.455 |
DOC_CKS1_1 | 433 | 438 | PF01111 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.279 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.202 |
DOC_MAPK_gen_1 | 271 | 280 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 863 | 872 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 273 | 282 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 4 | 11 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 865 | 874 | PF00069 | 0.427 |
DOC_PP2B_LxvP_1 | 683 | 686 | PF13499 | 0.490 |
DOC_PP4_MxPP_1 | 791 | 794 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.260 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.210 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.557 |
DOC_USP7_MATH_2 | 802 | 808 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.211 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 789 | 794 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 166 | 173 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 321 | 330 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 608 | 616 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 732 | 742 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 788 | 792 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 87 | 102 | PF00022 | 0.257 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.496 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.524 |
LIG_BIR_III_4 | 562 | 566 | PF00653 | 0.463 |
LIG_Clathr_ClatBox_1 | 869 | 873 | PF01394 | 0.430 |
LIG_CtBP_PxDLS_1 | 409 | 413 | PF00389 | 0.600 |
LIG_EH1_1 | 88 | 96 | PF00400 | 0.293 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.459 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.202 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.511 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.263 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.263 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.496 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.287 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.531 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.423 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.306 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.643 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.216 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.535 |
LIG_FHA_1 | 796 | 802 | PF00498 | 0.572 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.461 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.258 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.474 |
LIG_FHA_2 | 795 | 801 | PF00498 | 0.545 |
LIG_Integrin_RGD_1 | 227 | 229 | PF01839 | 0.251 |
LIG_Integrin_RGD_1 | 538 | 540 | PF01839 | 0.512 |
LIG_Integrin_RGD_1 | 771 | 773 | PF01839 | 0.526 |
LIG_LIR_Gen_1 | 368 | 379 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 694 | 698 | PF02991 | 0.650 |
LIG_MYND_1 | 583 | 587 | PF01753 | 0.514 |
LIG_NRBOX | 334 | 340 | PF00104 | 0.496 |
LIG_PCNA_yPIPBox_3 | 732 | 742 | PF02747 | 0.392 |
LIG_Pex14_2 | 69 | 73 | PF04695 | 0.293 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.293 |
LIG_SH2_CRK | 446 | 450 | PF00017 | 0.448 |
LIG_SH2_PTP2 | 135 | 138 | PF00017 | 0.293 |
LIG_SH2_PTP2 | 632 | 635 | PF00017 | 0.552 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.293 |
LIG_SH2_SRC | 58 | 61 | PF00017 | 0.258 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.258 |
LIG_SH2_STAT3 | 453 | 456 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 698 | 701 | PF00017 | 0.568 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.408 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.553 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.643 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.635 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 828 | 836 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 408 | 416 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.293 |
LIG_TRAF2_1 | 634 | 637 | PF00917 | 0.588 |
LIG_TRAF2_1 | 797 | 800 | PF00917 | 0.547 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.293 |
LIG_TYR_ITIM | 369 | 374 | PF00017 | 0.293 |
LIG_UBA3_1 | 433 | 438 | PF00899 | 0.430 |
MOD_CDC14_SPxK_1 | 615 | 618 | PF00782 | 0.630 |
MOD_CDK_SPK_2 | 579 | 584 | PF00069 | 0.509 |
MOD_CDK_SPxK_1 | 432 | 438 | PF00069 | 0.433 |
MOD_CDK_SPxK_1 | 612 | 618 | PF00069 | 0.632 |
MOD_CDK_SPxxK_3 | 391 | 398 | PF00069 | 0.556 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.230 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.209 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.467 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.496 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.560 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.638 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.458 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.409 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.632 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.409 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.474 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.576 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.433 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.616 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.409 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.535 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.602 |
MOD_CK2_1 | 804 | 810 | PF00069 | 0.566 |
MOD_Cter_Amidation | 396 | 399 | PF01082 | 0.493 |
MOD_Cter_Amidation | 652 | 655 | PF01082 | 0.543 |
MOD_DYRK1A_RPxSP_1 | 391 | 395 | PF00069 | 0.544 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.293 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.233 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.293 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.463 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.406 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.516 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.625 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.566 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.547 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.584 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.481 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.497 |
MOD_GlcNHglycan | 821 | 824 | PF01048 | 0.531 |
MOD_GlcNHglycan | 828 | 832 | PF01048 | 0.471 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.398 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.374 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.425 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.301 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.466 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.545 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.544 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.532 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.510 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.649 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.531 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.488 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.537 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.500 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.293 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.293 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.273 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.293 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.405 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.457 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.566 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.547 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.293 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.457 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.449 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.289 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.293 |
MOD_NEK2_2 | 520 | 525 | PF00069 | 0.434 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.442 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.619 |
MOD_PIKK_1 | 808 | 814 | PF00454 | 0.497 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.294 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.496 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.496 |
MOD_PKA_2 | 783 | 789 | PF00069 | 0.576 |
MOD_PKA_2 | 826 | 832 | PF00069 | 0.448 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.293 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.473 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.293 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.474 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.293 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.496 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.523 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.467 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.314 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.466 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.211 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.553 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.548 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.515 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.433 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.512 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.711 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.635 |
MOD_ProDKin_1 | 789 | 795 | PF00069 | 0.551 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 269 | 275 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 553 | 560 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 873 | 880 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 23 | 28 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.293 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 532 | 537 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.293 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.293 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.602 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.202 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 813 | 816 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 479 | 484 | PF00026 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IBS7 | Leishmania donovani | 24% | 100% |
A0A3Q8IEL2 | Leishmania donovani | 29% | 100% |
A0A3Q8IHG6 | Leishmania donovani | 29% | 100% |
A0A3S7WPL3 | Leishmania donovani | 74% | 99% |
A0A3S7X2P9 | Leishmania donovani | 29% | 100% |
A4HHN8 | Leishmania braziliensis | 28% | 100% |
A4HHY2 | Leishmania braziliensis | 25% | 100% |
A4HSZ5 | Leishmania infantum | 75% | 99% |
A4I4V2 | Leishmania infantum | 29% | 100% |
A4I4V3 | Leishmania infantum | 29% | 100% |
A4I562 | Leishmania infantum | 24% | 100% |
E9AEA0 | Leishmania major | 30% | 100% |
E9AEA1 | Leishmania major | 30% | 100% |
E9AKY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q0DV28 | Oryza sativa subsp. japonica | 25% | 93% |
Q4QIX3 | Leishmania major | 75% | 100% |