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: 19 |
NetGPI | no | yes: 0, no: 19 |
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: A4H8F0
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 | 20 |
GO:0003676 | nucleic acid binding | 3 | 20 |
GO:0003723 | RNA binding | 4 | 20 |
GO:0003824 | catalytic activity | 1 | 20 |
GO:0005488 | binding | 1 | 20 |
GO:0016407 | acetyltransferase activity | 5 | 20 |
GO:0016740 | transferase activity | 2 | 20 |
GO:0016746 | acyltransferase activity | 3 | 20 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 20 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043169 | cation binding | 3 | 20 |
GO:0046872 | metal ion binding | 4 | 20 |
GO:0051536 | iron-sulfur cluster binding | 3 | 20 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 20 |
GO:0051540 | metal cluster binding | 2 | 20 |
GO:0097159 | organic cyclic compound binding | 2 | 20 |
GO:0106261 | tRNA uridine(34) acetyltransferase activity | 6 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.493 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.282 |
CLV_C14_Caspase3-7 | 653 | 657 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 732 | 734 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 605 | 607 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 734 | 736 | PF00082 | 0.480 |
CLV_PCSK_PC7_1 | 628 | 634 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.184 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.316 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.445 |
DEG_COP1_1 | 134 | 143 | PF00400 | 0.563 |
DEG_SCF_FBW7_1 | 143 | 150 | PF00400 | 0.485 |
DOC_CDC14_PxL_1 | 28 | 36 | PF14671 | 0.394 |
DOC_CKS1_1 | 417 | 422 | PF01111 | 0.403 |
DOC_CKS1_1 | 556 | 561 | PF01111 | 0.246 |
DOC_CYCLIN_RxL_1 | 84 | 97 | PF00134 | 0.426 |
DOC_CYCLIN_yClb1_LxF_4 | 224 | 229 | PF00134 | 0.403 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 474 | 483 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 171 | 181 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 222 | 229 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 238 | 245 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.364 |
DOC_MAPK_gen_1 | 449 | 458 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 84 | 93 | PF00069 | 0.367 |
DOC_MAPK_HePTP_8 | 446 | 458 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 288 | 297 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 449 | 458 | PF00069 | 0.399 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.513 |
DOC_PP1_RVXF_1 | 224 | 230 | PF00149 | 0.403 |
DOC_PP2B_PxIxI_1 | 453 | 459 | PF00149 | 0.507 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.519 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.507 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.379 |
DOC_USP7_MATH_2 | 153 | 159 | PF00917 | 0.401 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.243 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 356 | 364 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 689 | 696 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 723 | 727 | PF00244 | 0.459 |
LIG_Actin_RPEL_3 | 682 | 701 | PF02755 | 0.393 |
LIG_Actin_WH2_2 | 668 | 685 | PF00022 | 0.434 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BIR_III_2 | 138 | 142 | PF00653 | 0.441 |
LIG_BIR_III_4 | 6 | 10 | PF00653 | 0.476 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.450 |
LIG_EH1_1 | 645 | 653 | PF00400 | 0.208 |
LIG_eIF4E_1 | 436 | 442 | PF01652 | 0.431 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.442 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.446 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.657 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.244 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.433 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.407 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.446 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.350 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.565 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.287 |
LIG_LIR_Apic_2 | 282 | 287 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 165 | 173 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 528 | 537 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 557 | 568 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 613 | 622 | PF02991 | 0.268 |
LIG_LIR_LC3C_4 | 177 | 182 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 528 | 534 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 557 | 563 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.239 |
LIG_MYND_3 | 31 | 35 | PF01753 | 0.406 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.391 |
LIG_NRBOX | 478 | 484 | PF00104 | 0.407 |
LIG_Pex14_1 | 199 | 203 | PF04695 | 0.403 |
LIG_Pex14_1 | 556 | 560 | PF04695 | 0.252 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.237 |
LIG_RPA_C_Fungi | 684 | 696 | PF08784 | 0.389 |
LIG_SH2_CRK | 575 | 579 | PF00017 | 0.282 |
LIG_SH2_CRK | 636 | 640 | PF00017 | 0.401 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.410 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 616 | 620 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 616 | 620 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.348 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.147 |
LIG_SH2_STAT3 | 414 | 417 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.231 |
LIG_SH3_1 | 202 | 208 | PF00018 | 0.237 |
LIG_SH3_2 | 151 | 156 | PF14604 | 0.449 |
LIG_SH3_2 | 287 | 292 | PF14604 | 0.383 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.599 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.677 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.717 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.392 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.261 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.313 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.292 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.296 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 250 | 256 | PF11976 | 0.261 |
LIG_SUMO_SIM_anti_2 | 617 | 623 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 650 | 656 | PF11976 | 0.302 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.520 |
LIG_UBA3_1 | 441 | 449 | PF00899 | 0.301 |
LIG_WW_3 | 285 | 289 | PF00397 | 0.182 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.546 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.662 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.269 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.491 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.430 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.431 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.273 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.258 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.520 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.292 |
MOD_CK2_1 | 744 | 750 | PF00069 | 0.552 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.725 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.487 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.372 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.315 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.299 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.430 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.237 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.534 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.601 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.697 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.695 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.302 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.260 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.297 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.261 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.459 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.250 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.517 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.498 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.555 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.345 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.237 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.317 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.252 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.271 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.273 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.617 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.389 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.594 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.417 |
MOD_NEK2_2 | 279 | 284 | PF00069 | 0.271 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.381 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.346 |
MOD_PIKK_1 | 663 | 669 | PF00454 | 0.411 |
MOD_PIKK_1 | 724 | 730 | PF00454 | 0.501 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.233 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.252 |
MOD_PKA_2 | 722 | 728 | PF00069 | 0.462 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.381 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.344 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.516 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.326 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.568 |
MOD_Plk_2-3 | 535 | 541 | PF00069 | 0.374 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.724 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.592 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.322 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.289 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.314 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.225 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.339 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.404 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.471 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.321 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.703 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.320 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.237 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.238 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.243 |
MOD_SUMO_rev_2 | 20 | 29 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 425 | 434 | PF00179 | 0.272 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 599 | 604 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 634 | 639 | PF01217 | 0.309 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.269 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 547 | 550 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.234 |
TRG_ER_diArg_1 | 682 | 684 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.555 |
TRG_ER_FFAT_2 | 40 | 52 | PF00635 | 0.319 |
TRG_NLS_MonoExtC_3 | 732 | 737 | PF00514 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.282 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFU7 | Leptomonas seymouri | 69% | 100% |
A0A0S4KPU1 | Bodo saltans | 56% | 100% |
A0A1X0NG94 | Trypanosomatidae | 60% | 100% |
A0A1X0NX69 | Trypanosomatidae | 45% | 100% |
A0A3Q8ICG0 | Leishmania donovani | 85% | 100% |
A0A3S7WXV4 | Leishmania donovani | 45% | 100% |
A0A422NDG5 | Trypanosoma rangeli | 60% | 100% |
A4HD08 | Leishmania braziliensis | 44% | 100% |
A4HWS3 | Leishmania infantum | 85% | 100% |
A4I0J4 | Leishmania infantum | 45% | 100% |
C9ZVC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZW50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
D5VRB9 | Methanocaldococcus infernus (strain DSM 11812 / JCM 15783 / ME) | 37% | 100% |
E9AQI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
E9AWF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q1ZXC6 | Dictyostelium discoideum | 33% | 100% |
Q2KJ61 | Bos taurus | 34% | 100% |
Q4QB17 | Leishmania major | 44% | 100% |
Q4QEZ6 | Leishmania major | 83% | 100% |
Q5HZM6 | Xenopus laevis | 35% | 100% |
Q5RIC0 | Danio rerio | 35% | 100% |
Q5ZHS1 | Gallus gallus | 35% | 100% |
Q6NVL5 | Xenopus tropicalis | 33% | 100% |
Q9CZX0 | Mus musculus | 33% | 100% |
Q9H9T3 | Homo sapiens | 33% | 100% |
V5B5L2 | Trypanosoma cruzi | 60% | 100% |
V5BNQ5 | Trypanosoma cruzi | 46% | 100% |