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: 2, no: 32 |
NetGPI | no | yes: 0, no: 34 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 35 |
GO:0016020 | membrane | 2 | 3 |
GO:0042995 | cell projection | 2 | 35 |
GO:0043226 | organelle | 2 | 35 |
GO:0043227 | membrane-bounded organelle | 3 | 35 |
GO:0110165 | cellular anatomical entity | 1 | 35 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 35 |
GO:0005743 | mitochondrial inner membrane | 5 | 1 |
GO:0019866 | organelle inner membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H3R1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016310 | phosphorylation | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006952 | defense response | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006457 | protein folding | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007021 | tubulin complex assembly | 6 | 1 |
GO:0007023 | post-chaperonin tubulin folding pathway | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004672 | protein kinase activity | 3 | 1 |
GO:0005488 | binding | 1 | 3 |
GO:0005524 | ATP binding | 5 | 1 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0043014 | alpha-tubulin binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.300 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.490 |
CLV_C14_Caspase3-7 | 555 | 559 | PF00656 | 0.242 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.374 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 677 | 679 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 674 | 678 | PF00082 | 0.521 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.352 |
DEG_ODPH_VHL_1 | 268 | 279 | PF01847 | 0.235 |
DEG_ODPH_VHL_1 | 403 | 414 | PF01847 | 0.226 |
DEG_ODPH_VHL_1 | 538 | 549 | PF01847 | 0.260 |
DOC_ANK_TNKS_1 | 677 | 684 | PF00023 | 0.508 |
DOC_CDC14_PxL_1 | 202 | 210 | PF14671 | 0.431 |
DOC_CDC14_PxL_1 | 316 | 324 | PF14671 | 0.323 |
DOC_CDC14_PxL_1 | 451 | 459 | PF14671 | 0.452 |
DOC_CDC14_PxL_1 | 496 | 504 | PF14671 | 0.253 |
DOC_CDC14_PxL_1 | 586 | 594 | PF14671 | 0.356 |
DOC_CDC14_PxL_1 | 631 | 639 | PF14671 | 0.467 |
DOC_CYCLIN_RxL_1 | 214 | 225 | PF00134 | 0.439 |
DOC_CYCLIN_RxL_1 | 427 | 436 | PF00134 | 0.299 |
DOC_CYCLIN_RxL_1 | 517 | 528 | PF00134 | 0.321 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 380 | 389 | PF00134 | 0.239 |
DOC_MAPK_gen_1 | 112 | 118 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 485 | 493 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 252 | 259 | PF00069 | 0.258 |
DOC_MAPK_MEF2A_6 | 36 | 44 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 95 | 104 | PF00069 | 0.333 |
DOC_PP1_RVXF_1 | 389 | 395 | PF00149 | 0.205 |
DOC_PP1_RVXF_1 | 76 | 83 | PF00149 | 0.386 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.535 |
DOC_USP7_UBL2_3 | 673 | 677 | PF12436 | 0.474 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 14 | 23 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 166 | 175 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 303 | 310 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 321 | 326 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 443 | 449 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 456 | 461 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 579 | 584 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 623 | 629 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.466 |
LIG_Actin_WH2_2 | 160 | 178 | PF00022 | 0.326 |
LIG_Actin_WH2_2 | 354 | 370 | PF00022 | 0.522 |
LIG_Actin_WH2_2 | 487 | 505 | PF00022 | 0.438 |
LIG_Actin_WH2_2 | 96 | 114 | PF00022 | 0.353 |
LIG_APCC_ABBA_1 | 62 | 67 | PF00400 | 0.311 |
LIG_APCC_ABBAyCdc20_2 | 429 | 435 | PF00400 | 0.246 |
LIG_BIR_III_4 | 71 | 75 | PF00653 | 0.313 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.259 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.406 |
LIG_Clathr_ClatBox_1 | 602 | 606 | PF01394 | 0.410 |
LIG_Clathr_ClatBox_1 | 614 | 618 | PF01394 | 0.428 |
LIG_DLG_GKlike_1 | 219 | 226 | PF00625 | 0.422 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.572 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.457 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.380 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.315 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.479 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.413 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.282 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.412 |
LIG_FHA_2 | 684 | 690 | PF00498 | 0.511 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.395 |
LIG_IBAR_NPY_1 | 154 | 156 | PF08397 | 0.425 |
LIG_LIR_Gen_1 | 124 | 132 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 570 | 578 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 149 | 153 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 570 | 574 | PF02991 | 0.206 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.589 |
LIG_MLH1_MIPbox_1 | 49 | 53 | PF16413 | 0.406 |
LIG_Pex14_2 | 106 | 110 | PF04695 | 0.466 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.406 |
LIG_RPA_C_Fungi | 667 | 679 | PF08784 | 0.465 |
LIG_SH2_PTP2 | 663 | 666 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.732 |
LIG_SUMO_SIM_anti_2 | 138 | 144 | PF11976 | 0.310 |
LIG_SUMO_SIM_anti_2 | 37 | 44 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 138 | 144 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 253 | 258 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 354 | 360 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 600 | 606 | PF11976 | 0.477 |
LIG_TRFH_1 | 151 | 155 | PF08558 | 0.420 |
LIG_TRFH_1 | 156 | 160 | PF08558 | 0.424 |
LIG_TYR_ITIM | 614 | 619 | PF00017 | 0.224 |
LIG_TYR_ITIM | 661 | 666 | PF00017 | 0.405 |
LIG_UBA3_1 | 31 | 36 | PF00899 | 0.334 |
MOD_CDK_SPxxK_3 | 361 | 368 | PF00069 | 0.240 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.543 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.492 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.421 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.414 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.435 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.492 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.614 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.430 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.254 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.400 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.478 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.490 |
MOD_CK2_1 | 683 | 689 | PF00069 | 0.519 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.578 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.312 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.436 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.401 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.366 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.493 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.359 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.319 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.345 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.467 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.367 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.526 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.671 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.405 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.484 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.456 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.392 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.361 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.408 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.400 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.450 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.528 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.389 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.427 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.327 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.326 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.575 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.496 |
MOD_LATS_1 | 12 | 18 | PF00433 | 0.268 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.427 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.410 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.240 |
MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.373 |
MOD_N-GLC_1 | 642 | 647 | PF02516 | 0.545 |
MOD_N-GLC_2 | 384 | 386 | PF02516 | 0.249 |
MOD_N-GLC_2 | 564 | 566 | PF02516 | 0.257 |
MOD_N-GLC_2 | 609 | 611 | PF02516 | 0.480 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.534 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.484 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.507 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.470 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.419 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.434 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.481 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.290 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.367 |
MOD_NEK2_2 | 182 | 187 | PF00069 | 0.306 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.247 |
MOD_OFUCOSY | 469 | 476 | PF10250 | 0.221 |
MOD_PK_1 | 278 | 284 | PF00069 | 0.403 |
MOD_PK_1 | 591 | 597 | PF00069 | 0.254 |
MOD_PKA_1 | 443 | 449 | PF00069 | 0.290 |
MOD_PKA_1 | 672 | 678 | PF00069 | 0.486 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.439 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.381 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.468 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.526 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.435 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.512 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.259 |
MOD_PKB_1 | 670 | 678 | PF00069 | 0.469 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.408 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.442 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.375 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.281 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.405 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.257 |
MOD_Plk_1 | 642 | 648 | PF00069 | 0.513 |
MOD_Plk_2-3 | 135 | 141 | PF00069 | 0.246 |
MOD_Plk_2-3 | 286 | 292 | PF00069 | 0.512 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.489 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.365 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.389 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.419 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.453 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.273 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.332 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.412 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.533 |
MOD_SUMO_rev_2 | 390 | 400 | PF00179 | 0.249 |
TRG_DiLeu_BaEn_1 | 489 | 494 | PF01217 | 0.295 |
TRG_DiLeu_BaEn_2 | 232 | 238 | PF01217 | 0.228 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.526 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.220 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 635 | 638 | PF00400 | 0.399 |
TRG_NES_CRM1_1 | 423 | 435 | PF08389 | 0.542 |
TRG_NLS_MonoExtN_4 | 670 | 676 | PF00514 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 14 | 19 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.271 |
TRG_Pf-PMV_PEXEL_1 | 430 | 435 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 520 | 525 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 648 | 652 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F9 | Leptomonas seymouri | 33% | 100% |
A0A0N0P8N9 | Leptomonas seymouri | 30% | 100% |
A0A0N1I0W0 | Leptomonas seymouri | 29% | 100% |
A0A0N1P921 | Leptomonas seymouri | 27% | 85% |
A0A0S4JC97 | Bodo saltans | 24% | 82% |
A0A0S4KN43 | Bodo saltans | 26% | 100% |
A0A1X0P4M6 | Trypanosomatidae | 23% | 100% |
A0A3Q8I8N4 | Leishmania donovani | 30% | 96% |
A0A3Q8IGD6 | Leishmania donovani | 23% | 85% |
A0A3S5H7C2 | Leishmania donovani | 26% | 100% |
A0A3S7X2V4 | Leishmania donovani | 69% | 90% |
A4H3H4 | Leishmania braziliensis | 27% | 71% |
A4H7G0 | Leishmania braziliensis | 29% | 94% |
A4I0G3 | Leishmania infantum | 26% | 100% |
A4I6T8 | Leishmania infantum | 23% | 85% |
C9ZK22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 85% |
D0A4F4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 82% |
E9ACE9 | Leishmania major | 26% | 69% |
E9AEF0 | Leishmania major | 69% | 100% |
E9AG21 | Leishmania infantum | 26% | 69% |
E9AGK6 | Leishmania infantum | 29% | 96% |
E9AGT5 | Leishmania infantum | 27% | 100% |
E9AHJ6 | Leishmania infantum | 69% | 90% |
E9AJN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 71% |
E9AKN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9APJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B1W0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 85% |
Q4Q6A2 | Leishmania major | 23% | 100% |
Q4QFY4 | Leishmania major | 30% | 96% |
Q4QJ77 | Leishmania major | 23% | 100% |
Q4QJ80 | Leishmania major | 27% | 100% |
V5BKI3 | Trypanosoma cruzi | 23% | 83% |
V5BXQ3 | Trypanosoma cruzi | 25% | 74% |