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: A4HMV4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 131 | 135 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 494 | 498 | PF00656 | 0.443 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 727 | 729 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.533 |
CLV_PCSK_FUR_1 | 100 | 104 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 210 | 212 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.598 |
DEG_APCC_DBOX_1 | 372 | 380 | PF00400 | 0.357 |
DEG_APCC_DBOX_1 | 405 | 413 | PF00400 | 0.427 |
DEG_SCF_FBW7_1 | 41 | 46 | PF00400 | 0.514 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.514 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.544 |
DEG_SPOP_SBC_1 | 75 | 79 | PF00917 | 0.631 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.543 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.534 |
DOC_CKS1_1 | 489 | 494 | PF01111 | 0.569 |
DOC_CKS1_1 | 571 | 576 | PF01111 | 0.477 |
DOC_MAPK_DCC_7 | 416 | 426 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 259 | 267 | PF00069 | 0.345 |
DOC_MAPK_gen_1 | 405 | 413 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 229 | 238 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.424 |
DOC_MAPK_RevD_3 | 247 | 260 | PF00069 | 0.332 |
DOC_MAPK_RevD_3 | 90 | 103 | PF00069 | 0.600 |
DOC_PP1_RVXF_1 | 619 | 625 | PF00149 | 0.500 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.532 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 716 | 720 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.504 |
DOC_USP7_MATH_2 | 306 | 312 | PF00917 | 0.464 |
DOC_USP7_UBL2_3 | 210 | 214 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 729 | 733 | PF12436 | 0.569 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 266 | 275 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 458 | 464 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 533 | 537 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 714 | 723 | PF00244 | 0.499 |
LIG_AP2alpha_1 | 495 | 499 | PF02296 | 0.564 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.532 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 61 | 65 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_2 | 414 | 420 | PF00533 | 0.468 |
LIG_Clathr_ClatBox_1 | 189 | 193 | PF01394 | 0.517 |
LIG_CtBP_PxDLS_1 | 537 | 541 | PF00389 | 0.566 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.525 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.507 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.711 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.369 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.670 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.466 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.566 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.472 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.443 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.611 |
LIG_FHA_1 | 716 | 722 | PF00498 | 0.380 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.638 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.441 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.500 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.390 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.562 |
LIG_LIR_Gen_1 | 181 | 192 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 415 | 426 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 556 | 564 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 609 | 620 | PF02991 | 0.422 |
LIG_LIR_LC3C_4 | 367 | 371 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.565 |
LIG_NRBOX | 230 | 236 | PF00104 | 0.314 |
LIG_NRBOX | 408 | 414 | PF00104 | 0.436 |
LIG_PCNA_PIPBox_1 | 605 | 614 | PF02747 | 0.558 |
LIG_Pex14_2 | 495 | 499 | PF04695 | 0.564 |
LIG_RPA_C_Fungi | 224 | 236 | PF08784 | 0.312 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.523 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.383 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 73 | 76 | PF00017 | 0.569 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.491 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.387 |
LIG_SH2_STAT3 | 118 | 121 | PF00017 | 0.545 |
LIG_SH2_STAT3 | 36 | 39 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.569 |
LIG_SH3_1 | 700 | 706 | PF00018 | 0.541 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.499 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.660 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.583 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.501 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.349 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.426 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.515 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.434 |
LIG_SH3_3 | 700 | 706 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.539 |
LIG_SUMO_SIM_anti_2 | 367 | 374 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 378 | 386 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 390 | 397 | PF11976 | 0.279 |
LIG_SUMO_SIM_anti_2 | 550 | 556 | PF11976 | 0.505 |
LIG_SUMO_SIM_anti_2 | 91 | 96 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 367 | 374 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 646 | 652 | PF11976 | 0.398 |
LIG_TYR_ITIM | 71 | 76 | PF00017 | 0.563 |
LIG_WRC_WIRS_1 | 503 | 508 | PF05994 | 0.480 |
LIG_WW_3 | 150 | 154 | PF00397 | 0.660 |
MOD_CDC14_SPxK_1 | 402 | 405 | PF00782 | 0.435 |
MOD_CDK_SPK_2 | 488 | 493 | PF00069 | 0.424 |
MOD_CDK_SPxK_1 | 399 | 405 | PF00069 | 0.422 |
MOD_CDK_SPxxK_3 | 146 | 153 | PF00069 | 0.538 |
MOD_CDK_SPxxK_3 | 399 | 406 | PF00069 | 0.415 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.659 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.581 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.543 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.562 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.536 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.529 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.452 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.508 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.621 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.419 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.683 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.481 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.421 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.359 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.460 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.541 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.502 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.398 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.503 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.729 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.600 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.607 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.820 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.581 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.478 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.323 |
MOD_GlcNHglycan | 517 | 521 | PF01048 | 0.543 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.646 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.576 |
MOD_GlcNHglycan | 661 | 665 | PF01048 | 0.614 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.531 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.412 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.642 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.804 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.567 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.567 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.355 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.538 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.704 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.560 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.480 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.537 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.533 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.519 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.559 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.545 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.473 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.586 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.436 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.742 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.508 |
MOD_N-GLC_1 | 677 | 682 | PF02516 | 0.545 |
MOD_N-GLC_1 | 695 | 700 | PF02516 | 0.430 |
MOD_N-GLC_1 | 716 | 721 | PF02516 | 0.537 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.580 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.466 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.371 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.459 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.559 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.556 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.479 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.487 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.410 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.515 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.556 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.507 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.568 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.579 |
MOD_NEK2_2 | 439 | 444 | PF00069 | 0.351 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.625 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.401 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.401 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.610 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.514 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.422 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.532 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.549 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.472 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.536 |
MOD_Plk_2-3 | 197 | 203 | PF00069 | 0.395 |
MOD_Plk_2-3 | 646 | 652 | PF00069 | 0.426 |
MOD_Plk_2-3 | 673 | 679 | PF00069 | 0.549 |
MOD_Plk_2-3 | 88 | 94 | PF00069 | 0.463 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.587 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.334 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.525 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.476 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.497 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.495 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.576 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.536 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.638 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.595 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.504 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.422 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.593 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.451 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.500 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.503 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.478 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.433 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.462 |
MOD_SUMO_for_1 | 613 | 616 | PF00179 | 0.525 |
TRG_DiLeu_BaEn_1 | 378 | 383 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.569 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.530 |
TRG_NLS_MonoExtC_3 | 727 | 732 | PF00514 | 0.583 |
TRG_NLS_MonoExtN_4 | 728 | 735 | PF00514 | 0.648 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.715 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 592 | 597 | PF00026 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFG5 | Leptomonas seymouri | 36% | 98% |
A0A3Q8IVC2 | Leishmania donovani | 62% | 100% |
A4IBH5 | Leishmania infantum | 62% | 100% |
E9AFB1 | Leishmania major | 63% | 100% |
E9B6G6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |