Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 5 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0034399 | nuclear periphery | 2 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:1990904 | ribonucleoprotein complex | 2 | 3 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0005730 | nucleolus | 5 | 2 |
Related structures:
AlphaFold database: A0A3S7WR01
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006364 | rRNA processing | 8 | 5 |
GO:0006396 | RNA processing | 6 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0016072 | rRNA metabolic process | 7 | 5 |
GO:0030490 | maturation of SSU-rRNA | 9 | 5 |
GO:0034470 | ncRNA processing | 7 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034660 | ncRNA metabolic process | 6 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 31 |
GO:0003676 | nucleic acid binding | 3 | 31 |
GO:0003824 | catalytic activity | 1 | 31 |
GO:0004386 | helicase activity | 2 | 31 |
GO:0005488 | binding | 1 | 31 |
GO:0005524 | ATP binding | 5 | 31 |
GO:0017076 | purine nucleotide binding | 4 | 31 |
GO:0030554 | adenyl nucleotide binding | 5 | 31 |
GO:0032553 | ribonucleotide binding | 3 | 31 |
GO:0032555 | purine ribonucleotide binding | 4 | 31 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 31 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 31 |
GO:0036094 | small molecule binding | 2 | 31 |
GO:0043167 | ion binding | 2 | 31 |
GO:0043168 | anion binding | 3 | 31 |
GO:0097159 | organic cyclic compound binding | 2 | 31 |
GO:0097367 | carbohydrate derivative binding | 2 | 31 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 31 |
GO:0140657 | ATP-dependent activity | 1 | 31 |
GO:1901265 | nucleoside phosphate binding | 3 | 31 |
GO:1901363 | heterocyclic compound binding | 2 | 31 |
GO:0003724 | RNA helicase activity | 3 | 17 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 17 |
GO:0016787 | hydrolase activity | 2 | 24 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 17 |
GO:0003743 | translation initiation factor activity | 4 | 9 |
GO:0008135 | translation factor activity, RNA binding | 3 | 9 |
GO:0045182 | translation regulator activity | 1 | 9 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 9 |
GO:0003723 | RNA binding | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 727 | 731 | PF00656 | 0.352 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 719 | 721 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 757 | 759 | PF00675 | 0.576 |
CLV_PCSK_FUR_1 | 755 | 759 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 627 | 629 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 757 | 759 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.207 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 627 | 629 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 651 | 653 | PF00082 | 0.206 |
CLV_PCSK_PC7_1 | 25 | 31 | PF00082 | 0.484 |
CLV_PCSK_PC7_1 | 753 | 759 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.465 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.478 |
DEG_APCC_DBOX_1 | 495 | 503 | PF00400 | 0.406 |
DEG_APCC_DBOX_1 | 556 | 564 | PF00400 | 0.330 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.470 |
DEG_SCF_FBW7_1 | 693 | 698 | PF00400 | 0.345 |
DEG_SPOP_SBC_1 | 385 | 389 | PF00917 | 0.415 |
DOC_ANK_TNKS_1 | 186 | 193 | PF00023 | 0.533 |
DOC_CKS1_1 | 455 | 460 | PF01111 | 0.526 |
DOC_CKS1_1 | 692 | 697 | PF01111 | 0.336 |
DOC_CYCLIN_yCln2_LP_2 | 13 | 19 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 327 | 334 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 446 | 455 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 534 | 542 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 584 | 590 | PF00069 | 0.494 |
DOC_MAPK_HePTP_8 | 532 | 544 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 535 | 544 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.506 |
DOC_PP2B_LxvP_1 | 609 | 612 | PF13499 | 0.437 |
DOC_PP4_FxxP_1 | 692 | 695 | PF00568 | 0.340 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 728 | 732 | PF00917 | 0.379 |
DOC_USP7_UBL2_3 | 363 | 367 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.335 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 685 | 695 | PF00244 | 0.413 |
LIG_Actin_WH2_2 | 395 | 413 | PF00022 | 0.408 |
LIG_APCC_ABBA_1 | 82 | 87 | PF00400 | 0.554 |
LIG_BRCT_BRCA1_1 | 688 | 692 | PF00533 | 0.345 |
LIG_CtBP_PxDLS_1 | 379 | 383 | PF00389 | 0.394 |
LIG_eIF4E_1 | 108 | 114 | PF01652 | 0.457 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.554 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.419 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.495 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.434 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.557 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.476 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.503 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.350 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.428 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.418 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.465 |
LIG_Integrin_isoDGR_2 | 494 | 496 | PF01839 | 0.206 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.569 |
LIG_LIR_Apic_2 | 689 | 695 | PF02991 | 0.333 |
LIG_LIR_Apic_2 | 732 | 738 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 342 | 353 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.594 |
LIG_PCNA_yPIPBox_3 | 355 | 369 | PF02747 | 0.406 |
LIG_PCNA_yPIPBox_3 | 709 | 723 | PF02747 | 0.359 |
LIG_Rb_LxCxE_1 | 243 | 262 | PF01857 | 0.486 |
LIG_Rb_LxCxE_1 | 519 | 538 | PF01857 | 0.309 |
LIG_Rb_pABgroove_1 | 571 | 579 | PF01858 | 0.347 |
LIG_RPA_C_Fungi | 182 | 194 | PF08784 | 0.514 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.289 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.262 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.323 |
LIG_SH2_CRK | 664 | 668 | PF00017 | 0.366 |
LIG_SH2_NCK_1 | 664 | 668 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.543 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.608 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.216 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.360 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.438 |
LIG_Sin3_3 | 344 | 351 | PF02671 | 0.212 |
LIG_SUMO_SIM_anti_2 | 541 | 547 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 476 | 481 | PF11976 | 0.243 |
LIG_SUMO_SIM_par_1 | 538 | 543 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 641 | 647 | PF11976 | 0.202 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.524 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.544 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.515 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.266 |
LIG_TRAF2_1 | 547 | 550 | PF00917 | 0.440 |
LIG_TRAF2_1 | 597 | 600 | PF00917 | 0.233 |
LIG_TYR_ITIM | 343 | 348 | PF00017 | 0.212 |
MOD_CDK_SPxK_1 | 454 | 460 | PF00069 | 0.380 |
MOD_CDK_SPxxK_3 | 209 | 216 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 489 | 496 | PF00069 | 0.219 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.553 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.411 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.402 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.307 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.497 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.210 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.417 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.340 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.616 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.262 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.504 |
MOD_CK1_1 | 731 | 737 | PF00069 | 0.518 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.669 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.608 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.380 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.456 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.246 |
MOD_Cter_Amidation | 755 | 758 | PF01082 | 0.540 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.556 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.701 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.662 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.406 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.356 |
MOD_GlcNHglycan | 337 | 341 | PF01048 | 0.368 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.219 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.258 |
MOD_GlcNHglycan | 39 | 43 | PF01048 | 0.571 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.195 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.185 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.646 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.278 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.341 |
MOD_GlcNHglycan | 681 | 685 | PF01048 | 0.489 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.519 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.602 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.522 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.547 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.424 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.283 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.297 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.604 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.427 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.393 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.274 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.278 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.661 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.334 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.400 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.528 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.497 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.584 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.538 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.523 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.414 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.275 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.535 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.266 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.390 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.474 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.559 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.485 |
MOD_PIKK_1 | 675 | 681 | PF00454 | 0.219 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.527 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.537 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.390 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.265 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.282 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.315 |
MOD_PKA_2 | 675 | 681 | PF00069 | 0.332 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.459 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.623 |
MOD_Plk_1 | 731 | 737 | PF00069 | 0.497 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.487 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.422 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.560 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.292 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.492 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.305 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.251 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.304 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.450 |
MOD_Plk_4 | 731 | 737 | PF00069 | 0.443 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.473 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.542 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.518 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.387 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.246 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.362 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.332 |
MOD_SUMO_rev_2 | 360 | 365 | PF00179 | 0.195 |
MOD_SUMO_rev_2 | 772 | 779 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 422 | 427 | PF01217 | 0.257 |
TRG_DiLeu_BaEn_4 | 360 | 366 | PF01217 | 0.202 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.262 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.230 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.219 |
TRG_ER_diArg_1 | 752 | 755 | PF00400 | 0.609 |
TRG_ER_diLys_1 | 776 | 780 | PF00400 | 0.485 |
TRG_NES_CRM1_1 | 665 | 675 | PF08389 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 758 | 762 | PF00026 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5R1 | Leptomonas seymouri | 58% | 98% |
A0A3Q8ID91 | Leishmania donovani | 28% | 100% |
A0A3Q8IF94 | Leishmania donovani | 24% | 100% |
A0A3Q8IQY6 | Leishmania donovani | 25% | 100% |
A0A3S5H5X3 | Leishmania donovani | 24% | 100% |
A0A3S7X579 | Leishmania donovani | 26% | 100% |
A1CHL3 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 22% | 98% |
A4H4Y0 | Leishmania braziliensis | 24% | 100% |
A4H5Z5 | Leishmania braziliensis | 69% | 98% |
A4HGR1 | Leishmania braziliensis | 28% | 100% |
A4HK20 | Leishmania braziliensis | 24% | 100% |
A4HK38 | Leishmania braziliensis | 25% | 100% |
A4HP82 | Leishmania braziliensis | 25% | 100% |
A4HTF8 | Leishmania infantum | 27% | 100% |
A4HUC1 | Leishmania infantum | 99% | 100% |
A4HZF8 | Leishmania infantum | 21% | 100% |
A4I3T6 | Leishmania infantum | 28% | 100% |
A4I7K4 | Leishmania infantum | 24% | 100% |
A4I7M5 | Leishmania infantum | 26% | 100% |
A4IDI7 | Leishmania infantum | 25% | 100% |
A5DF03 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 22% | 100% |
E9AM86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AN20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9ASZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AT30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B2I0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
P0CQ88 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 100% |
P0CQ89 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 100% |
Q4Q1G8 | Leishmania major | 23% | 100% |
Q4Q1K8 | Leishmania major | 25% | 100% |
Q4Q5M6 | Leishmania major | 26% | 100% |
Q4Q5P5 | Leishmania major | 24% | 100% |
Q4Q858 | Leishmania major | 28% | 100% |
Q4QHK6 | Leishmania major | 91% | 100% |
Q4QIG1 | Leishmania major | 27% | 100% |
Q4QIQ9 | Leishmania major | 24% | 100% |