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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B2R1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006370 | 7-methylguanosine mRNA capping | 8 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006397 | mRNA processing | 7 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009452 | 7-methylguanosine RNA capping | 8 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0016071 | mRNA metabolic process | 6 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0036260 | RNA capping | 7 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004484 | mRNA guanylyltransferase activity | 5 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0008192 | RNA guanylyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016779 | nucleotidyltransferase activity | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0070568 | guanylyltransferase activity | 5 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0005525 | GTP binding | 5 | 4 |
GO:0019001 | guanyl nucleotide binding | 5 | 4 |
GO:0019002 | GMP binding | 4 | 1 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 4 |
GO:0003909 | DNA ligase activity | 4 | 1 |
GO:0003910 | DNA ligase (ATP) activity | 5 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.352 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 475 | 477 | PF00082 | 0.426 |
CLV_PCSK_PC7_1 | 370 | 376 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.458 |
CLV_Separin_Metazoa | 484 | 488 | PF03568 | 0.303 |
DEG_APCC_DBOX_1 | 155 | 163 | PF00400 | 0.457 |
DEG_SCF_FBW7_1 | 60 | 65 | PF00400 | 0.530 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.579 |
DOC_CDC14_PxL_1 | 514 | 522 | PF14671 | 0.303 |
DOC_CKS1_1 | 313 | 318 | PF01111 | 0.405 |
DOC_CYCLIN_RxL_1 | 548 | 562 | PF00134 | 0.353 |
DOC_CYCLIN_RxL_1 | 669 | 677 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 223 | 229 | PF00134 | 0.292 |
DOC_CYCLIN_yCln2_LP_2 | 401 | 407 | PF00134 | 0.303 |
DOC_MAPK_gen_1 | 191 | 200 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 269 | 279 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 304 | 311 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 374 | 381 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 644 | 652 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 609 | 618 | PF00069 | 0.384 |
DOC_MAPK_RevD_3 | 274 | 289 | PF00069 | 0.392 |
DOC_PP1_RVXF_1 | 670 | 677 | PF00149 | 0.403 |
DOC_PP2B_LxvP_1 | 223 | 226 | PF13499 | 0.293 |
DOC_PP4_FxxP_1 | 676 | 679 | PF00568 | 0.420 |
DOC_PP4_MxPP_1 | 35 | 38 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.735 |
DOC_USP7_UBL2_3 | 548 | 552 | PF12436 | 0.271 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.755 |
LIG_14-3-3_CanoR_1 | 375 | 380 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 609 | 616 | PF00244 | 0.387 |
LIG_Actin_WH2_2 | 224 | 242 | PF00022 | 0.384 |
LIG_Actin_WH2_2 | 594 | 611 | PF00022 | 0.402 |
LIG_APCC_ABBA_1 | 595 | 600 | PF00400 | 0.381 |
LIG_APCC_Cbox_2 | 201 | 207 | PF00515 | 0.398 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.693 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.609 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.245 |
LIG_EH1_1 | 528 | 536 | PF00400 | 0.303 |
LIG_eIF4E_1 | 320 | 326 | PF01652 | 0.379 |
LIG_eIF4E_1 | 411 | 417 | PF01652 | 0.271 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.437 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.281 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.204 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.516 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.476 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.426 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.221 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.391 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.563 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.447 |
LIG_Integrin_RGD_1 | 245 | 247 | PF01839 | 0.513 |
LIG_LIR_Apic_2 | 115 | 120 | PF02991 | 0.623 |
LIG_LIR_Apic_2 | 26 | 31 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 155 | 162 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 321 | 329 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 377 | 385 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 412 | 421 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 423 | 431 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 465 | 474 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 481 | 490 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 576 | 584 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 663 | 668 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 465 | 469 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 576 | 581 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 663 | 667 | PF02991 | 0.451 |
LIG_MYND_1 | 518 | 522 | PF01753 | 0.303 |
LIG_PCNA_APIM_2 | 546 | 552 | PF02747 | 0.303 |
LIG_PCNA_TLS_4 | 543 | 550 | PF02747 | 0.303 |
LIG_Pex14_2 | 403 | 407 | PF04695 | 0.253 |
LIG_Pex14_2 | 413 | 417 | PF04695 | 0.253 |
LIG_Pex14_2 | 422 | 426 | PF04695 | 0.253 |
LIG_Pex14_2 | 549 | 553 | PF04695 | 0.271 |
LIG_REV1ctd_RIR_1 | 477 | 486 | PF16727 | 0.387 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.434 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.329 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.338 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.255 |
LIG_SH2_PTP2 | 380 | 383 | PF00017 | 0.303 |
LIG_SH2_PTP2 | 511 | 514 | PF00017 | 0.271 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.372 |
LIG_SH2_SRC | 390 | 393 | PF00017 | 0.175 |
LIG_SH2_SRC | 511 | 514 | PF00017 | 0.253 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.255 |
LIG_SH2_STAT3 | 212 | 215 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 257 | 260 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.253 |
LIG_SH3_1 | 310 | 316 | PF00018 | 0.356 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.478 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.709 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.490 |
LIG_SH3_3 | 639 | 645 | PF00018 | 0.453 |
LIG_SUMO_SIM_par_1 | 610 | 617 | PF11976 | 0.467 |
LIG_TRAF2_1 | 663 | 666 | PF00917 | 0.369 |
LIG_TYR_ITIM | 662 | 667 | PF00017 | 0.446 |
LIG_UBA3_1 | 297 | 304 | PF00899 | 0.479 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.756 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.460 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.559 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.796 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.687 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.483 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.438 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.571 |
MOD_CK2_1 | 648 | 654 | PF00069 | 0.470 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.288 |
MOD_Cter_Amidation | 122 | 125 | PF01082 | 0.539 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.698 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.617 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.599 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.342 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.573 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.144 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.447 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.364 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.395 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.406 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.704 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.373 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.701 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.616 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.603 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.564 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.480 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.424 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.289 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.221 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.307 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.753 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.790 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.557 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.662 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.478 |
MOD_N-GLC_1 | 679 | 684 | PF02516 | 0.523 |
MOD_N-GLC_2 | 219 | 221 | PF02516 | 0.320 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.426 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.284 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.303 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.215 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.311 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.406 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.420 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.704 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.422 |
MOD_PIKK_1 | 630 | 636 | PF00454 | 0.614 |
MOD_PK_1 | 293 | 299 | PF00069 | 0.359 |
MOD_PKA_1 | 374 | 380 | PF00069 | 0.303 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.517 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.303 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.547 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.428 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.434 |
MOD_Plk_2-3 | 573 | 579 | PF00069 | 0.556 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.459 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.303 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.271 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.303 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.405 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.391 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.666 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.529 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.404 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.303 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.753 |
MOD_SUMO_rev_2 | 164 | 174 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 366 | 376 | PF00179 | 0.398 |
TRG_DiLeu_BaEn_1 | 155 | 160 | PF01217 | 0.457 |
TRG_DiLeu_BaEn_1 | 481 | 486 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_1 | 488 | 493 | PF01217 | 0.247 |
TRG_DiLeu_BaEn_1 | 516 | 521 | PF01217 | 0.255 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 456 | 461 | PF01217 | 0.303 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.144 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 664 | 667 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 639 | 642 | PF00400 | 0.447 |
TRG_NES_CRM1_1 | 222 | 237 | PF08389 | 0.369 |
TRG_NLS_Bipartite_1 | 288 | 308 | PF00514 | 0.389 |
TRG_NLS_MonoExtN_4 | 303 | 308 | PF00514 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IM27 | Bodo saltans | 34% | 95% |
A0A1X0NUI5 | Trypanosomatidae | 39% | 100% |
A0A3S7X5E2 | Leishmania donovani | 91% | 99% |
A0A422P1D1 | Trypanosoma rangeli | 41% | 100% |
A4HKC4 | Leishmania braziliensis | 83% | 100% |
D0AA12 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
Q4Q5E6 | Leishmania major | 92% | 100% |
V5DHN7 | Trypanosoma cruzi | 42% | 100% |