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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
GO:0005874 | microtubule | 6 | 4 |
GO:0099080 | supramolecular complex | 2 | 4 |
GO:0099081 | supramolecular polymer | 3 | 4 |
GO:0099512 | supramolecular fiber | 4 | 4 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 4 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AUL7
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 24 |
GO:0008152 | metabolic process | 1 | 24 |
GO:0019538 | protein metabolic process | 3 | 24 |
GO:0036211 | protein modification process | 4 | 24 |
GO:0043170 | macromolecule metabolic process | 3 | 24 |
GO:0043412 | macromolecule modification | 4 | 24 |
GO:0044238 | primary metabolic process | 2 | 24 |
GO:0071704 | organic substance metabolic process | 2 | 24 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 24 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 3 |
GO:0006996 | organelle organization | 4 | 3 |
GO:0007010 | cytoskeleton organization | 5 | 3 |
GO:0007017 | microtubule-based process | 2 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0018095 | protein polyglutamylation | 7 | 6 |
GO:0018193 | peptidyl-amino acid modification | 5 | 6 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 21 |
GO:0016874 | ligase activity | 2 | 21 |
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 6 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 7 |
GO:0016881 | acid-amino acid ligase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:0005515 | protein binding | 2 | 3 |
GO:0008092 | cytoskeletal protein binding | 3 | 3 |
GO:0015631 | tubulin binding | 4 | 3 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 3 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.371 |
CLV_C14_Caspase3-7 | 695 | 699 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 706 | 710 | PF00656 | 0.309 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.386 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.190 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.339 |
CLV_Separin_Metazoa | 495 | 499 | PF03568 | 0.539 |
DEG_APCC_DBOX_1 | 404 | 412 | PF00400 | 0.550 |
DEG_APCC_DBOX_1 | 582 | 590 | PF00400 | 0.526 |
DEG_SPOP_SBC_1 | 9 | 13 | PF00917 | 0.576 |
DOC_CYCLIN_yCln2_LP_2 | 620 | 623 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 198 | 206 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 35 | 43 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 687 | 694 | PF00069 | 0.600 |
DOC_MAPK_JIP1_4 | 583 | 589 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 35 | 43 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 383 | 391 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 492 | 501 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 583 | 591 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 707 | 716 | PF00069 | 0.255 |
DOC_MAPK_NFAT4_5 | 384 | 392 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 496 | 502 | PF00149 | 0.456 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.421 |
DOC_PP4_MxPP_1 | 621 | 624 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.701 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 122 | 126 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 410 | 415 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 418 | 427 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 513 | 520 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 652 | 659 | PF00244 | 0.511 |
LIG_Actin_WH2_2 | 497 | 515 | PF00022 | 0.445 |
LIG_APCC_ABBA_1 | 401 | 406 | PF00400 | 0.469 |
LIG_APCC_ABBAyCdc20_2 | 400 | 406 | PF00400 | 0.431 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.526 |
LIG_EH_1 | 375 | 379 | PF12763 | 0.526 |
LIG_EH1_1 | 552 | 560 | PF00400 | 0.442 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.434 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.479 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.460 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.463 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.541 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.534 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.451 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.639 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.408 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.583 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.444 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.442 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.332 |
LIG_FHA_2 | 663 | 669 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 245 | 250 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 481 | 487 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 132 | 141 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 547 | 558 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 596 | 606 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 673 | 680 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 596 | 602 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 673 | 678 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 686 | 691 | PF02991 | 0.389 |
LIG_MLH1_MIPbox_1 | 546 | 550 | PF16413 | 0.421 |
LIG_NRBOX | 201 | 207 | PF00104 | 0.428 |
LIG_PCNA_PIPBox_1 | 592 | 601 | PF02747 | 0.459 |
LIG_PCNA_yPIPBox_3 | 365 | 374 | PF02747 | 0.401 |
LIG_Pex14_2 | 549 | 553 | PF04695 | 0.494 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.393 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.529 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.520 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.471 |
LIG_SH2_CRK | 688 | 692 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 46 | 50 | PF00017 | 0.471 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 368 | 371 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.525 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.427 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.481 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.717 |
LIG_SH3_4 | 276 | 283 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 556 | 566 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 613 | 619 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 556 | 568 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 583 | 588 | PF11976 | 0.472 |
LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.408 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.745 |
LIG_TRAF2_1 | 633 | 636 | PF00917 | 0.459 |
LIG_TRAF2_1 | 664 | 667 | PF00917 | 0.342 |
LIG_TYR_ITSM | 392 | 399 | PF00017 | 0.421 |
MOD_CDC14_SPxK_1 | 32 | 35 | PF00782 | 0.464 |
MOD_CDK_SPxK_1 | 29 | 35 | PF00069 | 0.473 |
MOD_CDK_SPxK_1 | 701 | 707 | PF00069 | 0.578 |
MOD_CDK_SPxxK_3 | 29 | 36 | PF00069 | 0.504 |
MOD_CDK_SPxxK_3 | 411 | 418 | PF00069 | 0.408 |
MOD_CDK_SPxxK_3 | 502 | 509 | PF00069 | 0.526 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.706 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.559 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.503 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.570 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.457 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.461 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.497 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.593 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.412 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.492 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.454 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.543 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.732 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.673 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.471 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.408 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.500 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.720 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.477 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.368 |
MOD_Cter_Amidation | 196 | 199 | PF01082 | 0.231 |
MOD_Cter_Amidation | 381 | 384 | PF01082 | 0.335 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.665 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.651 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.338 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.324 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.390 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.255 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.195 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.330 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.261 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.311 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.369 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.581 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.383 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.618 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.525 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.771 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.515 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.533 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.572 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.530 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.488 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.480 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.507 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.545 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.559 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.516 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.508 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.473 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.500 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.625 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.649 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.267 |
MOD_N-GLC_1 | 441 | 446 | PF02516 | 0.257 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.272 |
MOD_N-GLC_1 | 543 | 548 | PF02516 | 0.201 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.510 |
MOD_N-GLC_1 | 645 | 650 | PF02516 | 0.335 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.349 |
MOD_N-GLC_2 | 660 | 662 | PF02516 | 0.320 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.416 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.428 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.407 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.457 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.477 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.447 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.539 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.535 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.523 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.535 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.398 |
MOD_PKA_1 | 337 | 343 | PF00069 | 0.494 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.484 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.548 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.410 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.586 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.522 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.548 |
MOD_PKB_1 | 337 | 345 | PF00069 | 0.391 |
MOD_PKB_1 | 517 | 525 | PF00069 | 0.371 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.446 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.521 |
MOD_Plk_1 | 645 | 651 | PF00069 | 0.336 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.488 |
MOD_Plk_2-3 | 565 | 571 | PF00069 | 0.371 |
MOD_Plk_2-3 | 651 | 657 | PF00069 | 0.338 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.667 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.499 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.443 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.493 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.499 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.561 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.460 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.425 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.536 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.331 |
MOD_Plk_4 | 710 | 716 | PF00069 | 0.418 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.532 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.352 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.483 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.445 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.610 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.442 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.494 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.506 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.391 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.462 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.518 |
MOD_SUMO_rev_2 | 246 | 255 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 432 | 438 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 464 | 471 | PF00179 | 0.426 |
TRG_DiLeu_BaEn_1 | 495 | 500 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 164 | 169 | PF01217 | 0.278 |
TRG_DiLeu_BaLyEn_6 | 674 | 679 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 688 | 691 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 517 | 520 | PF00400 | 0.422 |
TRG_NES_CRM1_1 | 495 | 507 | PF08389 | 0.455 |
TRG_NES_CRM1_1 | 551 | 563 | PF08389 | 0.421 |
TRG_NLS_MonoExtC_3 | 34 | 39 | PF00514 | 0.353 |
TRG_NLS_MonoExtN_4 | 33 | 39 | PF00514 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.257 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.208 |
TRG_Pf-PMV_PEXEL_1 | 689 | 693 | PF00026 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7G7 | Leptomonas seymouri | 43% | 88% |
A0A0N1I1Q6 | Leptomonas seymouri | 27% | 100% |
A0A0S4ISF0 | Bodo saltans | 26% | 100% |
A0A0S4KQK8 | Bodo saltans | 29% | 100% |
A0A1X0NXX8 | Trypanosomatidae | 31% | 99% |
A0A3Q8IDL7 | Leishmania donovani | 89% | 99% |
A0A3Q8IEC1 | Leishmania donovani | 28% | 100% |
A0A422NPL9 | Trypanosoma rangeli | 33% | 100% |
A4H8G3 | Leishmania braziliensis | 24% | 98% |
A4HG29 | Leishmania braziliensis | 24% | 100% |
A4HWT7 | Leishmania infantum | 25% | 88% |
A4HYN9 | Leishmania infantum | 89% | 99% |
A4I5Q6 | Leishmania infantum | 28% | 100% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZR25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AID0 | Leishmania braziliensis | 76% | 100% |
E9AM52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AQJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 88% |
E9B101 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4Q765 | Leishmania major | 26% | 100% |
Q4QCW7 | Leishmania major | 90% | 100% |
Q4QEY2 | Leishmania major | 24% | 89% |