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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0033588 | elongator holoenzyme complex | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:0005819 | spindle | 5 | 1 |
Related structures:
AlphaFold database: A0A3Q8ICG0
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 2 |
GO:0002098 | tRNA wobble uridine modification | 8 | 2 |
GO:0002926 | tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation | 9 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006475 | internal protein amino acid acetylation | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008033 | tRNA processing | 8 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016573 | histone acetylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0018393 | internal peptidyl-lysine acetylation | 8 | 1 |
GO:0018394 | peptidyl-lysine acetylation | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043007 | maintenance of rDNA | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0043570 | maintenance of DNA repeat elements | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 19 |
GO:0003676 | nucleic acid binding | 3 | 19 |
GO:0003723 | RNA binding | 4 | 19 |
GO:0003824 | catalytic activity | 1 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0016407 | acetyltransferase activity | 5 | 19 |
GO:0016740 | transferase activity | 2 | 19 |
GO:0016746 | acyltransferase activity | 3 | 19 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 19 |
GO:0043167 | ion binding | 2 | 19 |
GO:0043169 | cation binding | 3 | 19 |
GO:0046872 | metal ion binding | 4 | 19 |
GO:0051536 | iron-sulfur cluster binding | 3 | 19 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 19 |
GO:0051540 | metal cluster binding | 2 | 19 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
GO:0106261 | tRNA uridine(34) acetyltransferase activity | 6 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.327 |
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.371 |
CLV_C14_Caspase3-7 | 652 | 656 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 632 | 634 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 733 | 735 | PF00082 | 0.524 |
CLV_PCSK_PC7_1 | 628 | 634 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.476 |
DOC_ANK_TNKS_1 | 744 | 751 | PF00023 | 0.469 |
DOC_CDC14_PxL_1 | 28 | 36 | PF14671 | 0.403 |
DOC_CKS1_1 | 155 | 160 | PF01111 | 0.637 |
DOC_CKS1_1 | 417 | 422 | PF01111 | 0.435 |
DOC_CKS1_1 | 556 | 561 | PF01111 | 0.272 |
DOC_CKS1_1 | 589 | 594 | PF01111 | 0.199 |
DOC_CYCLIN_yClb1_LxF_4 | 224 | 229 | PF00134 | 0.435 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 474 | 483 | PF00134 | 0.445 |
DOC_MAPK_gen_1 | 171 | 181 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 222 | 229 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 238 | 245 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 291 | 297 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 449 | 458 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 84 | 93 | PF00069 | 0.401 |
DOC_MAPK_HePTP_8 | 446 | 458 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 449 | 458 | PF00069 | 0.431 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.516 |
DOC_PP1_RVXF_1 | 224 | 230 | PF00149 | 0.435 |
DOC_PP2B_PxIxI_1 | 453 | 459 | PF00149 | 0.540 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.517 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.540 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 743 | 747 | PF00917 | 0.493 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.250 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 688 | 693 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 722 | 726 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 667 | 684 | PF00022 | 0.515 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_BIR_III_4 | 747 | 751 | PF00653 | 0.463 |
LIG_eIF4E_1 | 436 | 442 | PF01652 | 0.463 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.780 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.460 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.580 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.754 |
LIG_FHA_1 | 710 | 716 | PF00498 | 0.559 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.474 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.442 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.488 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.582 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.514 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.316 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.534 |
LIG_LIR_Apic_2 | 262 | 267 | PF02991 | 0.423 |
LIG_LIR_Apic_2 | 282 | 287 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 165 | 173 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 528 | 537 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 557 | 568 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 613 | 622 | PF02991 | 0.313 |
LIG_LIR_LC3C_4 | 177 | 182 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 528 | 534 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 557 | 563 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.284 |
LIG_MYND_3 | 31 | 35 | PF01753 | 0.411 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.397 |
LIG_NRBOX | 478 | 484 | PF00104 | 0.438 |
LIG_Pex14_1 | 199 | 203 | PF04695 | 0.435 |
LIG_Pex14_1 | 556 | 560 | PF04695 | 0.281 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.267 |
LIG_SH2_CRK | 575 | 579 | PF00017 | 0.325 |
LIG_SH2_CRK | 616 | 620 | PF00017 | 0.270 |
LIG_SH2_CRK | 636 | 640 | PF00017 | 0.455 |
LIG_SH2_CRK | 718 | 722 | PF00017 | 0.431 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 616 | 620 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 616 | 620 | PF00017 | 0.320 |
LIG_SH2_STAT3 | 414 | 417 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.405 |
LIG_SH3_1 | 202 | 208 | PF00018 | 0.435 |
LIG_SH3_2 | 287 | 292 | PF14604 | 0.540 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.710 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.412 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.459 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.502 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.484 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.360 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.375 |
LIG_SUMO_SIM_anti_2 | 250 | 256 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 617 | 623 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.375 |
LIG_SxIP_EBH_1 | 688 | 701 | PF03271 | 0.519 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.551 |
LIG_TRAF2_1 | 516 | 519 | PF00917 | 0.362 |
LIG_TRAF2_1 | 611 | 614 | PF00917 | 0.250 |
LIG_UBA3_1 | 441 | 449 | PF00899 | 0.281 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.560 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.639 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.686 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.312 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.641 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.325 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.264 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.444 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.321 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.573 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.552 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.734 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.779 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.705 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.411 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.354 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.326 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.474 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.346 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.267 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.594 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.764 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.530 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.731 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.330 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.290 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.279 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.300 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.494 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.699 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.602 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.365 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.267 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.718 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.527 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.354 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.281 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.312 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.279 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.628 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.461 |
MOD_NEK2_2 | 279 | 284 | PF00069 | 0.300 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.519 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.384 |
MOD_PIKK_1 | 614 | 620 | PF00454 | 0.458 |
MOD_PIKK_1 | 709 | 715 | PF00454 | 0.616 |
MOD_PK_1 | 688 | 694 | PF00069 | 0.493 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.532 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.324 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.658 |
MOD_PKA_2 | 721 | 727 | PF00069 | 0.502 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.343 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.379 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.656 |
MOD_Plk_2-3 | 4 | 10 | PF00069 | 0.586 |
MOD_Plk_2-3 | 535 | 541 | PF00069 | 0.405 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.360 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.330 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.362 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.266 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.368 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.342 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.730 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.678 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.688 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.333 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.349 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.192 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.267 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.271 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.250 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.683 |
MOD_SUMO_for_1 | 665 | 668 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 20 | 29 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 425 | 434 | PF00179 | 0.272 |
TRG_DiLeu_BaEn_3 | 52 | 58 | PF01217 | 0.343 |
TRG_DiLeu_BaEn_4 | 584 | 590 | PF01217 | 0.199 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 599 | 604 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 634 | 639 | PF01217 | 0.348 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 718 | 721 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 547 | 550 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 681 | 683 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.583 |
TRG_NLS_MonoExtC_3 | 731 | 736 | PF00514 | 0.646 |
TRG_NLS_MonoExtC_3 | 80 | 85 | PF00514 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFU7 | Leptomonas seymouri | 71% | 100% |
A0A0S4KPU1 | Bodo saltans | 59% | 100% |
A0A1X0NG94 | Trypanosomatidae | 61% | 100% |
A0A1X0NX69 | Trypanosomatidae | 45% | 100% |
A0A3S7WXV4 | Leishmania donovani | 46% | 100% |
A0A422NDG5 | Trypanosoma rangeli | 61% | 100% |
A4H8F0 | Leishmania braziliensis | 85% | 100% |
A4HD08 | Leishmania braziliensis | 45% | 100% |
A4HWS3 | Leishmania infantum | 100% | 100% |
A4I0J4 | Leishmania infantum | 46% | 100% |
C9ZVC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZW50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AQI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AWF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
Q4QB17 | Leishmania major | 46% | 100% |
Q4QEZ6 | Leishmania major | 94% | 100% |
V5B5L2 | Trypanosoma cruzi | 60% | 100% |