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: 15 |
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: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 3 |
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 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005739 | mitochondrion | 5 | 2 |
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 |
Related structures:
AlphaFold database: A0A3Q8IG57
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902775 | mitochondrial large ribosomal subunit assembly | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 22 |
GO:0003676 | nucleic acid binding | 3 | 22 |
GO:0003824 | catalytic activity | 1 | 22 |
GO:0004386 | helicase activity | 2 | 22 |
GO:0005488 | binding | 1 | 22 |
GO:0005524 | ATP binding | 5 | 22 |
GO:0017076 | purine nucleotide binding | 4 | 22 |
GO:0030554 | adenyl nucleotide binding | 5 | 22 |
GO:0032553 | ribonucleotide binding | 3 | 22 |
GO:0032555 | purine ribonucleotide binding | 4 | 22 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 22 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 22 |
GO:0036094 | small molecule binding | 2 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043168 | anion binding | 3 | 22 |
GO:0097159 | organic cyclic compound binding | 2 | 22 |
GO:0097367 | carbohydrate derivative binding | 2 | 22 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 22 |
GO:0140657 | ATP-dependent activity | 1 | 22 |
GO:1901265 | nucleoside phosphate binding | 3 | 22 |
GO:1901363 | heterocyclic compound binding | 2 | 22 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0003724 | RNA helicase activity | 3 | 6 |
GO:0003743 | translation initiation factor activity | 4 | 5 |
GO:0008135 | translation factor activity, RNA binding | 3 | 5 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 6 |
GO:0045182 | translation regulator activity | 1 | 5 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 6 |
GO:0003723 | RNA binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.802 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 766 | 768 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.717 |
CLV_PCSK_FUR_1 | 747 | 751 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 766 | 768 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.751 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.399 |
CLV_PCSK_PC7_1 | 347 | 353 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.190 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.553 |
DEG_APCC_DBOX_1 | 209 | 217 | PF00400 | 0.366 |
DEG_APCC_DBOX_1 | 406 | 414 | PF00400 | 0.503 |
DEG_APCC_DBOX_1 | 501 | 509 | PF00400 | 0.450 |
DEG_APCC_DBOX_1 | 558 | 566 | PF00400 | 0.541 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.785 |
DEG_SPOP_SBC_1 | 546 | 550 | PF00917 | 0.481 |
DOC_CYCLIN_RxL_1 | 473 | 483 | PF00134 | 0.449 |
DOC_CYCLIN_RxL_1 | 492 | 500 | PF00134 | 0.414 |
DOC_CYCLIN_yClb1_LxF_4 | 475 | 480 | PF00134 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 184 | 190 | PF00134 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 508 | 514 | PF00134 | 0.659 |
DOC_CYCLIN_yCln2_LP_2 | 720 | 723 | PF00134 | 0.419 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 84 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 347 | 356 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 470 | 480 | PF00069 | 0.481 |
DOC_MAPK_JIP1_4 | 474 | 480 | PF00069 | 0.461 |
DOC_PP1_RVXF_1 | 475 | 481 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 561 | 568 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 575 | 581 | PF00149 | 0.300 |
DOC_PP1_RVXF_1 | 590 | 597 | PF00149 | 0.537 |
DOC_PP1_RVXF_1 | 652 | 659 | PF00149 | 0.448 |
DOC_PP1_SILK_1 | 206 | 211 | PF00149 | 0.370 |
DOC_PP2B_LxvP_1 | 184 | 187 | PF13499 | 0.556 |
DOC_PP2B_LxvP_1 | 508 | 511 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 720 | 723 | PF13499 | 0.419 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 698 | 701 | PF00568 | 0.357 |
DOC_PP4_FxxP_1 | 742 | 745 | PF00568 | 0.558 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.642 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 755 | 760 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 433 | 439 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 639 | 647 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 9 | 19 | PF00244 | 0.552 |
LIG_Actin_WH2_2 | 129 | 147 | PF00022 | 0.533 |
LIG_Actin_WH2_2 | 254 | 269 | PF00022 | 0.475 |
LIG_Actin_WH2_2 | 71 | 89 | PF00022 | 0.510 |
LIG_AP2alpha_1 | 733 | 737 | PF02296 | 0.557 |
LIG_APCC_ABBA_1 | 313 | 318 | PF00400 | 0.544 |
LIG_BIR_III_2 | 122 | 126 | PF00653 | 0.499 |
LIG_BIR_III_4 | 113 | 117 | PF00653 | 0.659 |
LIG_BIR_III_4 | 182 | 186 | PF00653 | 0.559 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.421 |
LIG_EH1_1 | 391 | 399 | PF00400 | 0.451 |
LIG_eIF4E_1 | 256 | 262 | PF01652 | 0.544 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.630 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.480 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.459 |
LIG_FHA_1 | 756 | 762 | PF00498 | 0.723 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.520 |
LIG_FHA_2 | 669 | 675 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 330 | 335 | PF02991 | 0.521 |
LIG_LIR_Apic_2 | 697 | 701 | PF02991 | 0.351 |
LIG_LIR_Apic_2 | 740 | 745 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 732 | 741 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 657 | 661 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 732 | 736 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.743 |
LIG_NRBOX | 260 | 266 | PF00104 | 0.544 |
LIG_OCRL_FandH_1 | 384 | 396 | PF00620 | 0.451 |
LIG_PCNA_PIPBox_1 | 773 | 782 | PF02747 | 0.578 |
LIG_Pex14_2 | 733 | 737 | PF04695 | 0.557 |
LIG_PTB_Apo_2 | 736 | 743 | PF02174 | 0.587 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.497 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.570 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.506 |
LIG_SH2_CRK | 667 | 671 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 667 | 671 | PF00017 | 0.501 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.544 |
LIG_SH2_STAT3 | 713 | 716 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 728 | 731 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.519 |
LIG_SH3_2 | 745 | 750 | PF14604 | 0.622 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.769 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.606 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.499 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.534 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.563 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.554 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.749 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.576 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.578 |
LIG_SUMO_SIM_par_1 | 177 | 182 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 199 | 205 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 233 | 238 | PF11976 | 0.446 |
LIG_TRAF2_1 | 402 | 405 | PF00917 | 0.461 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.544 |
LIG_TYR_ITIM | 487 | 492 | PF00017 | 0.438 |
LIG_UBA3_1 | 261 | 267 | PF00899 | 0.544 |
LIG_UBA3_1 | 427 | 435 | PF00899 | 0.461 |
LIG_UBA3_1 | 464 | 470 | PF00899 | 0.448 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.451 |
LIG_WRC_WIRS_1 | 695 | 700 | PF05994 | 0.433 |
LIG_WW_3 | 721 | 725 | PF00397 | 0.359 |
MOD_CDC14_SPxK_1 | 530 | 533 | PF00782 | 0.562 |
MOD_CDK_SPxK_1 | 527 | 533 | PF00069 | 0.561 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.834 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.478 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.445 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.451 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.581 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.630 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.450 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.498 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.469 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.457 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.449 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.451 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.449 |
MOD_DYRK1A_RPxSP_1 | 223 | 227 | PF00069 | 0.366 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.750 |
MOD_GlcNHglycan | 171 | 175 | PF01048 | 0.507 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.232 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.344 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.208 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.286 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.819 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.798 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.801 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.515 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.504 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.578 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.679 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.614 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.449 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.459 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.513 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.486 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.646 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.735 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.339 |
MOD_N-GLC_1 | 737 | 742 | PF02516 | 0.598 |
MOD_N-GLC_1 | 755 | 760 | PF02516 | 0.792 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.660 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.497 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.504 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.562 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.552 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.492 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.489 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.479 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.540 |
MOD_NEK2_2 | 694 | 699 | PF00069 | 0.324 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.728 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.538 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.640 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.605 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.463 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.561 |
MOD_PK_1 | 160 | 166 | PF00069 | 0.575 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.575 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.508 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.606 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.461 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.521 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.521 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.599 |
MOD_Plk_2-3 | 668 | 674 | PF00069 | 0.474 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.522 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.435 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.451 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.471 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.539 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.518 |
MOD_Plk_4 | 694 | 700 | PF00069 | 0.388 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.495 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.518 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.496 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.574 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.528 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.389 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.501 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.705 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.759 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.663 |
MOD_ProDKin_1 | 755 | 761 | PF00069 | 0.651 |
TRG_DiLeu_BaEn_1 | 365 | 370 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.597 |
TRG_DiLeu_BaLyEn_6 | 474 | 479 | PF01217 | 0.448 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 696 | 699 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 723 | 726 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 747 | 750 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 765 | 767 | PF00400 | 0.681 |
TRG_NLS_MonoExtN_4 | 219 | 224 | PF00514 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I458 | Leptomonas seymouri | 74% | 100% |
A0A0N1I5R1 | Leptomonas seymouri | 21% | 99% |
A0A0S4JPF4 | Bodo saltans | 39% | 100% |
A0A1X0P7J3 | Trypanosomatidae | 56% | 100% |
A0A3Q8ID91 | Leishmania donovani | 26% | 100% |
A0A3Q8IF94 | Leishmania donovani | 26% | 100% |
A4HGR1 | Leishmania braziliensis | 27% | 100% |
A4HK20 | Leishmania braziliensis | 26% | 100% |
A4HPB9 | Leishmania braziliensis | 86% | 100% |
A4I3T6 | Leishmania infantum | 26% | 100% |
A4I7K4 | Leishmania infantum | 26% | 100% |
A4ICF9 | Leishmania infantum | 100% | 100% |
D0A3C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AT30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q1G8 | Leishmania major | 94% | 99% |
Q4Q5P5 | Leishmania major | 26% | 100% |
Q4Q858 | Leishmania major | 26% | 100% |
V5D8J9 | Trypanosoma cruzi | 57% | 100% |