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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
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:0110165 | cellular anatomical entity | 1 | 3 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:0005819 | spindle | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AQI1
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 | 18 |
GO:0003676 | nucleic acid binding | 3 | 18 |
GO:0003723 | RNA binding | 4 | 18 |
GO:0003824 | catalytic activity | 1 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0016407 | acetyltransferase activity | 5 | 18 |
GO:0016740 | transferase activity | 2 | 18 |
GO:0016746 | acyltransferase activity | 3 | 18 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043169 | cation binding | 3 | 18 |
GO:0046872 | metal ion binding | 4 | 18 |
GO:0051536 | iron-sulfur cluster binding | 3 | 18 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 18 |
GO:0051540 | metal cluster binding | 2 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
GO:0106261 | tRNA uridine(34) acetyltransferase activity | 6 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.497 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 742 | 744 | PF00082 | 0.481 |
CLV_PCSK_PC7_1 | 637 | 643 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.197 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.193 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.304 |
DEG_APCC_DBOX_1 | 300 | 308 | PF00400 | 0.436 |
DEG_SCF_FBW7_1 | 150 | 156 | PF00400 | 0.470 |
DOC_CDC14_PxL_1 | 28 | 36 | PF14671 | 0.370 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.454 |
DOC_CKS1_1 | 426 | 431 | PF01111 | 0.397 |
DOC_CKS1_1 | 565 | 570 | PF01111 | 0.233 |
DOC_CYCLIN_yClb1_LxF_4 | 233 | 238 | PF00134 | 0.397 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 483 | 492 | PF00134 | 0.406 |
DOC_MAPK_gen_1 | 180 | 190 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 231 | 238 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 247 | 254 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 300 | 306 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 458 | 467 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 84 | 93 | PF00069 | 0.376 |
DOC_MAPK_HePTP_8 | 455 | 467 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 458 | 467 | PF00069 | 0.397 |
DOC_PP1_RVXF_1 | 173 | 180 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 233 | 239 | PF00149 | 0.397 |
DOC_PP2B_PxIxI_1 | 462 | 468 | PF00149 | 0.502 |
DOC_PP4_FxxP_1 | 179 | 182 | PF00568 | 0.487 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.291 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.231 |
DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.217 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 522 | 527 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 697 | 706 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 731 | 735 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 473 | 491 | PF00022 | 0.336 |
LIG_Actin_WH2_2 | 676 | 693 | PF00022 | 0.462 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.596 |
LIG_eIF4E_1 | 445 | 451 | PF01652 | 0.423 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.425 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.554 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.680 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.410 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.445 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.411 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.437 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.550 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.577 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.472 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.272 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.495 |
LIG_LIR_Apic_2 | 271 | 276 | PF02991 | 0.391 |
LIG_LIR_Apic_2 | 291 | 296 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 174 | 182 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 427 | 437 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 537 | 546 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 566 | 577 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 622 | 631 | PF02991 | 0.289 |
LIG_LIR_LC3C_4 | 186 | 191 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 237 | 241 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 566 | 572 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 622 | 628 | PF02991 | 0.260 |
LIG_MYND_3 | 31 | 35 | PF01753 | 0.378 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.362 |
LIG_Pex14_1 | 208 | 212 | PF04695 | 0.397 |
LIG_Pex14_1 | 565 | 569 | PF04695 | 0.239 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.225 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.296 |
LIG_SH2_CRK | 625 | 629 | PF00017 | 0.232 |
LIG_SH2_CRK | 645 | 649 | PF00017 | 0.469 |
LIG_SH2_CRK | 727 | 731 | PF00017 | 0.399 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.399 |
LIG_SH2_NCK_1 | 625 | 629 | PF00017 | 0.275 |
LIG_SH2_STAP1 | 625 | 629 | PF00017 | 0.275 |
LIG_SH2_STAT3 | 423 | 426 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.427 |
LIG_SH3_1 | 211 | 217 | PF00018 | 0.397 |
LIG_SH3_2 | 296 | 301 | PF14604 | 0.502 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.667 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.378 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.427 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.480 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.451 |
LIG_SH3_3 | 540 | 546 | PF00018 | 0.281 |
LIG_SH3_3 | 703 | 709 | PF00018 | 0.458 |
LIG_SUMO_SIM_anti_2 | 186 | 192 | PF11976 | 0.341 |
LIG_SUMO_SIM_anti_2 | 259 | 265 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 626 | 632 | PF11976 | 0.275 |
LIG_SUMO_SIM_par_1 | 186 | 192 | PF11976 | 0.341 |
LIG_TRAF2_1 | 525 | 528 | PF00917 | 0.331 |
LIG_TRAF2_1 | 620 | 623 | PF00917 | 0.217 |
LIG_TRAF2_1 | 755 | 758 | PF00917 | 0.470 |
LIG_UBA3_1 | 450 | 458 | PF00899 | 0.286 |
LIG_WRC_WIRS_1 | 588 | 593 | PF05994 | 0.140 |
MOD_CDK_SPxxK_3 | 158 | 165 | PF00069 | 0.527 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.720 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.460 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.628 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.600 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.622 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.283 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.267 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.259 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.628 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.256 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.527 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.401 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.304 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.545 |
MOD_CK2_1 | 752 | 758 | PF00069 | 0.548 |
MOD_Cter_Amidation | 739 | 742 | PF01082 | 0.349 |
MOD_DYRK1A_RPxSP_1 | 597 | 601 | PF00069 | 0.175 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.763 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.738 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.661 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.366 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.319 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.284 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.461 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.447 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.324 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.225 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.536 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.542 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.720 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.504 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.671 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.577 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.323 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.254 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.304 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.267 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.254 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.659 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.538 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.315 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.225 |
MOD_N-GLC_1 | 695 | 700 | PF02516 | 0.656 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.372 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.322 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.239 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.281 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.258 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.588 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.454 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.256 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.342 |
MOD_PIKK_1 | 623 | 629 | PF00454 | 0.446 |
MOD_PIKK_1 | 718 | 724 | PF00454 | 0.576 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.521 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.239 |
MOD_PKA_2 | 730 | 736 | PF00069 | 0.456 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.522 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.319 |
MOD_Plk_1 | 679 | 685 | PF00069 | 0.587 |
MOD_Plk_2-3 | 4 | 10 | PF00069 | 0.553 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.557 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.330 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.314 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.361 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.225 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.307 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.682 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.646 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.315 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.308 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.225 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.245 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.231 |
MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.217 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 20 | 29 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 434 | 443 | PF00179 | 0.279 |
TRG_DiLeu_BaEn_3 | 52 | 58 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.384 |
TRG_DiLeu_BaLyEn_6 | 608 | 613 | PF01217 | 0.316 |
TRG_DiLeu_BaLyEn_6 | 643 | 648 | PF01217 | 0.318 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 645 | 648 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 727 | 730 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.247 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 506 | 509 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 529 | 531 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 556 | 559 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 640 | 643 | PF00400 | 0.244 |
TRG_ER_diArg_1 | 690 | 692 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.546 |
TRG_NLS_MonoExtC_3 | 740 | 745 | PF00514 | 0.599 |
TRG_NLS_MonoExtC_3 | 80 | 85 | PF00514 | 0.422 |
TRG_NLS_MonoExtN_4 | 78 | 85 | PF00514 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 469 | 473 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 59 | 63 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 658 | 662 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFU7 | Leptomonas seymouri | 70% | 100% |
A0A0S4KPU1 | Bodo saltans | 60% | 100% |
A0A1X0NG94 | Trypanosomatidae | 59% | 100% |
A0A3Q8ICG0 | Leishmania donovani | 92% | 100% |
A0A3S7WXV4 | Leishmania donovani | 46% | 100% |
A0A422NDG5 | Trypanosoma rangeli | 60% | 100% |
A4H8F0 | Leishmania braziliensis | 81% | 99% |
A4HD08 | Leishmania braziliensis | 45% | 100% |
A4HWS3 | Leishmania infantum | 92% | 100% |
A4I0J4 | Leishmania infantum | 46% | 100% |
C9ZW50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AWF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
Q23651 | Caenorhabditis elegans | 33% | 100% |
Q2KJ61 | Bos taurus | 33% | 100% |
Q4QB17 | Leishmania major | 46% | 100% |
Q4QEZ6 | Leishmania major | 92% | 99% |
Q5HZM6 | Xenopus laevis | 34% | 100% |
Q5RIC0 | Danio rerio | 34% | 100% |
Q5ZHS1 | Gallus gallus | 33% | 100% |
Q60LW7 | Caenorhabditis briggsae | 34% | 100% |
Q6NVL5 | Xenopus tropicalis | 33% | 100% |
Q93ZR1 | Arabidopsis thaliana | 35% | 100% |
Q9CZX0 | Mus musculus | 32% | 100% |
Q9H9T3 | Homo sapiens | 33% | 100% |
V5B5L2 | Trypanosoma cruzi | 70% | 100% |
V5BNQ5 | Trypanosoma cruzi | 46% | 100% |