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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000428 | DNA-directed RNA polymerase complex | 4 | 2 |
GO:0005658 | alpha DNA polymerase:primase complex | 4 | 2 |
GO:0030880 | RNA polymerase complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0042575 | DNA polymerase complex | 3 | 2 |
GO:0055029 | nuclear DNA-directed RNA polymerase complex | 3 | 2 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
GO:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q5A8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006270 | DNA replication initiation | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006260 | DNA replication | 5 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.675 |
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 559 | 563 | PF00656 | 0.809 |
CLV_C14_Caspase3-7 | 611 | 615 | PF00656 | 0.748 |
CLV_C14_Caspase3-7 | 658 | 662 | PF00656 | 0.692 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 599 | 601 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.399 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.540 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.449 |
DEG_APCC_DBOX_1 | 412 | 420 | PF00400 | 0.423 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.680 |
DEG_SCF_FBW7_1 | 625 | 631 | PF00400 | 0.752 |
DEG_SPOP_SBC_1 | 214 | 218 | PF00917 | 0.749 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.648 |
DEG_SPOP_SBC_1 | 563 | 567 | PF00917 | 0.689 |
DOC_ANK_TNKS_1 | 554 | 561 | PF00023 | 0.688 |
DOC_CDC14_PxL_1 | 517 | 525 | PF14671 | 0.550 |
DOC_CKS1_1 | 622 | 627 | PF01111 | 0.749 |
DOC_CYCLIN_RxL_1 | 378 | 386 | PF00134 | 0.364 |
DOC_CYCLIN_RxL_1 | 417 | 425 | PF00134 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.662 |
DOC_MAPK_DCC_7 | 633 | 642 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 518 | 525 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 633 | 642 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.583 |
DOC_MAPK_RevD_3 | 692 | 708 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 331 | 337 | PF00149 | 0.443 |
DOC_PP2B_LxvP_1 | 30 | 33 | PF13499 | 0.651 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.363 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.403 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.242 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.710 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.659 |
LIG_14-3-3_CanoR_1 | 251 | 255 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 257 | 262 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 351 | 358 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 55 | 60 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 707 | 716 | PF00244 | 0.567 |
LIG_AP2alpha_2 | 276 | 278 | PF02296 | 0.539 |
LIG_BIR_III_4 | 114 | 118 | PF00653 | 0.687 |
LIG_BIR_III_4 | 605 | 609 | PF00653 | 0.724 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 686 | 690 | PF00533 | 0.656 |
LIG_Clathr_ClatBox_1 | 16 | 20 | PF01394 | 0.737 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.668 |
LIG_DLG_GKlike_1 | 55 | 62 | PF00625 | 0.619 |
LIG_eIF4E_1 | 410 | 416 | PF01652 | 0.449 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.682 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.382 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.449 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.379 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.547 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.724 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.622 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.651 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.712 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.342 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.328 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.558 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.705 |
LIG_Integrin_isoDGR_2 | 500 | 502 | PF01839 | 0.475 |
LIG_Integrin_RGD_1 | 427 | 429 | PF01839 | 0.398 |
LIG_LIR_Apic_2 | 293 | 297 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.668 |
LIG_LIR_Gen_1 | 390 | 399 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 573 | 583 | PF02991 | 0.672 |
LIG_LIR_LC3C_4 | 672 | 677 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.673 |
LIG_MYND_1 | 29 | 33 | PF01753 | 0.731 |
LIG_NRBOX | 12 | 18 | PF00104 | 0.602 |
LIG_PALB2_WD40_1 | 257 | 265 | PF16756 | 0.488 |
LIG_PDZ_Class_2 | 721 | 726 | PF00595 | 0.651 |
LIG_Pex14_1 | 576 | 580 | PF04695 | 0.760 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.449 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.359 |
LIG_SH2_CRK | 59 | 63 | PF00017 | 0.639 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 504 | 507 | PF00017 | 0.398 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.449 |
LIG_SH2_SRC | 527 | 530 | PF00017 | 0.641 |
LIG_SH2_SRC | 636 | 639 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 77 | 80 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.615 |
LIG_SH3_2 | 300 | 305 | PF14604 | 0.635 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.735 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.405 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.547 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.409 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.348 |
LIG_SH3_3 | 616 | 622 | PF00018 | 0.807 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 363 | 368 | PF11976 | 0.361 |
LIG_SUMO_SIM_anti_2 | 672 | 678 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 40 | 47 | PF11976 | 0.714 |
LIG_SUMO_SIM_par_1 | 420 | 425 | PF11976 | 0.334 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.706 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.655 |
LIG_TRAF2_1 | 401 | 404 | PF00917 | 0.364 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.740 |
LIG_UBA3_1 | 415 | 420 | PF00899 | 0.449 |
LIG_UBA3_1 | 534 | 538 | PF00899 | 0.633 |
LIG_WRC_WIRS_1 | 395 | 400 | PF05994 | 0.437 |
MOD_CDK_SPK_2 | 684 | 689 | PF00069 | 0.642 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.635 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.419 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.399 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.531 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.686 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.777 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.724 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.680 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.687 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.515 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.525 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.608 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.678 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.379 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.263 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.344 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.608 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.776 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.630 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.664 |
MOD_GlcNHglycan | 145 | 149 | PF01048 | 0.617 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.717 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.486 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.499 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.634 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.637 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.337 |
MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.378 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.647 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.650 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.707 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.787 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.599 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.586 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.493 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.647 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.656 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.500 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.592 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.686 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.347 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.312 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.348 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.699 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.671 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.685 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.620 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.378 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.526 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.741 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.735 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.467 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.362 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.320 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.441 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.449 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.554 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.537 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.640 |
MOD_NEK2_2 | 487 | 492 | PF00069 | 0.449 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.550 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.380 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.572 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.369 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.328 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.661 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.693 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.691 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.678 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.606 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.400 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.549 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.363 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.575 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.603 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.712 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.495 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.350 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.315 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.479 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.689 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.400 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.430 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.358 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.340 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.579 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.790 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.657 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.641 |
MOD_SUMO_for_1 | 601 | 604 | PF00179 | 0.682 |
MOD_SUMO_for_1 | 688 | 691 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 530 | 540 | PF00179 | 0.676 |
TRG_DiLeu_BaEn_1 | 27 | 32 | PF01217 | 0.662 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.704 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.717 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.217 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 706 | 708 | PF00400 | 0.595 |
TRG_NLS_MonoExtC_3 | 598 | 604 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 597 | 603 | PF00514 | 0.694 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAT5 | Leptomonas seymouri | 64% | 100% |
A0A0S4JBE4 | Bodo saltans | 31% | 100% |
A0A1X0NW10 | Trypanosomatidae | 42% | 100% |
A0A3Q8IL35 | Leishmania donovani | 91% | 100% |
A0A3R7NGI8 | Trypanosoma rangeli | 42% | 100% |
A4HKF9 | Leishmania braziliensis | 76% | 100% |
A4I7Y7 | Leishmania infantum | 91% | 100% |
D0AA49 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B2U8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DFV4 | Trypanosoma cruzi | 41% | 100% |