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: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 4 |
GO:0005739 | mitochondrion | 5 | 3 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0005634 | nucleus | 5 | 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:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 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 |
Related structures:
AlphaFold database: Q4Q1G8
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 2 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1902775 | mitochondrial large ribosomal subunit assembly | 8 | 2 |
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 | 26 |
GO:0003676 | nucleic acid binding | 3 | 26 |
GO:0003824 | catalytic activity | 1 | 26 |
GO:0004386 | helicase activity | 2 | 26 |
GO:0005488 | binding | 1 | 26 |
GO:0005524 | ATP binding | 5 | 26 |
GO:0017076 | purine nucleotide binding | 4 | 26 |
GO:0030554 | adenyl nucleotide binding | 5 | 26 |
GO:0032553 | ribonucleotide binding | 3 | 26 |
GO:0032555 | purine ribonucleotide binding | 4 | 26 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 26 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 26 |
GO:0036094 | small molecule binding | 2 | 26 |
GO:0043167 | ion binding | 2 | 26 |
GO:0043168 | anion binding | 3 | 26 |
GO:0097159 | organic cyclic compound binding | 2 | 26 |
GO:0097367 | carbohydrate derivative binding | 2 | 26 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 26 |
GO:0140657 | ATP-dependent activity | 1 | 26 |
GO:1901265 | nucleoside phosphate binding | 3 | 26 |
GO:1901363 | heterocyclic compound binding | 2 | 26 |
GO:0003723 | RNA binding | 4 | 3 |
GO:0016787 | hydrolase activity | 2 | 11 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.745 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 668 | 670 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 685 | 687 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.696 |
CLV_PCSK_FUR_1 | 271 | 275 | PF00082 | 0.187 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 685 | 687 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.187 |
CLV_PCSK_PC7_1 | 266 | 272 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.184 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.187 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.376 |
DEG_APCC_DBOX_1 | 134 | 142 | PF00400 | 0.349 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.478 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.394 |
DEG_APCC_DBOX_1 | 477 | 485 | PF00400 | 0.534 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.486 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.193 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.453 |
DOC_CYCLIN_RxL_1 | 393 | 402 | PF00134 | 0.430 |
DOC_CYCLIN_RxL_1 | 411 | 419 | PF00134 | 0.394 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.510 |
DOC_CYCLIN_yCln2_LP_2 | 427 | 433 | PF00134 | 0.577 |
DOC_CYCLIN_yCln2_LP_2 | 639 | 642 | PF00134 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 95 | 101 | PF00134 | 0.644 |
DOC_MAPK_JIP1_4 | 393 | 399 | PF00069 | 0.439 |
DOC_PP1_RVXF_1 | 494 | 500 | PF00149 | 0.285 |
DOC_PP1_RVXF_1 | 509 | 516 | PF00149 | 0.509 |
DOC_PP1_RVXF_1 | 571 | 578 | PF00149 | 0.429 |
DOC_PP1_SILK_1 | 131 | 136 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 639 | 642 | PF13499 | 0.398 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.667 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.496 |
DOC_PP4_FxxP_1 | 617 | 620 | PF00568 | 0.354 |
DOC_PP4_FxxP_1 | 661 | 664 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.694 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 358 | 364 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 441 | 446 | PF00244 | 0.788 |
LIG_14-3-3_CanoR_1 | 558 | 566 | PF00244 | 0.520 |
LIG_Actin_WH2_2 | 179 | 194 | PF00022 | 0.452 |
LIG_Actin_WH2_2 | 53 | 71 | PF00022 | 0.500 |
LIG_AP2alpha_1 | 652 | 656 | PF02296 | 0.490 |
LIG_APCC_ABBA_1 | 232 | 237 | PF00400 | 0.521 |
LIG_BIR_III_4 | 107 | 111 | PF00653 | 0.531 |
LIG_BIR_III_4 | 37 | 41 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.412 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.378 |
LIG_EH1_1 | 310 | 318 | PF00400 | 0.425 |
LIG_eIF4E_1 | 181 | 187 | PF01652 | 0.521 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.494 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.456 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.480 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.682 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.546 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.482 |
LIG_LIR_Apic_2 | 249 | 254 | PF02991 | 0.496 |
LIG_LIR_Apic_2 | 616 | 620 | PF02991 | 0.345 |
LIG_LIR_Apic_2 | 659 | 664 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 419 | 430 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 651 | 660 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 163 | 167 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.714 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 651 | 655 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 684 | 690 | PF02991 | 0.583 |
LIG_NRBOX | 185 | 191 | PF00104 | 0.478 |
LIG_OCRL_FandH_1 | 303 | 315 | PF00620 | 0.425 |
LIG_PCNA_PIPBox_1 | 692 | 701 | PF02747 | 0.523 |
LIG_Pex14_2 | 652 | 656 | PF04695 | 0.490 |
LIG_PTB_Apo_2 | 655 | 662 | PF02174 | 0.529 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.460 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.543 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.508 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.505 |
LIG_SH2_NCK_1 | 586 | 590 | PF00017 | 0.496 |
LIG_SH2_SRC | 181 | 184 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 632 | 635 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 647 | 650 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.545 |
LIG_SH3_2 | 664 | 669 | PF14604 | 0.581 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.310 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.483 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.503 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.540 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.554 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.570 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.769 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.719 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.537 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.572 |
LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 124 | 130 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 423 | 429 | PF11976 | 0.413 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.440 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.526 |
LIG_TYR_ITIM | 406 | 411 | PF00017 | 0.399 |
LIG_UBA3_1 | 186 | 192 | PF00899 | 0.532 |
LIG_UBA3_1 | 346 | 354 | PF00899 | 0.439 |
LIG_UBA3_1 | 383 | 389 | PF00899 | 0.421 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.425 |
LIG_WRC_WIRS_1 | 614 | 619 | PF05994 | 0.400 |
LIG_WW_3 | 640 | 644 | PF00397 | 0.342 |
MOD_CDC14_SPxK_1 | 449 | 452 | PF00782 | 0.546 |
MOD_CDK_SPxK_1 | 446 | 452 | PF00069 | 0.546 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.433 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.727 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.427 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.612 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.448 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.457 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.461 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.429 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.587 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.437 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.450 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.704 |
MOD_DYRK1A_RPxSP_1 | 148 | 152 | PF00069 | 0.338 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.739 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.248 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.407 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.627 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.259 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.634 |
MOD_GlcNHglycan | 46 | 50 | PF01048 | 0.695 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.578 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.265 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.711 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.484 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.690 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.487 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.650 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.646 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.630 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.453 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.423 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.513 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.462 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.187 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.321 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.500 |
MOD_N-GLC_1 | 674 | 679 | PF02516 | 0.545 |
MOD_N-GLC_2 | 480 | 482 | PF02516 | 0.285 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.771 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.507 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.472 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.425 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.540 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.520 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.466 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.453 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.543 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.481 |
MOD_NEK2_2 | 613 | 618 | PF00069 | 0.300 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.610 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.428 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.477 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.531 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.620 |
MOD_PK_1 | 85 | 91 | PF00069 | 0.554 |
MOD_PKA_1 | 85 | 91 | PF00069 | 0.556 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.439 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.501 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.646 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.765 |
MOD_Plk_1 | 536 | 542 | PF00069 | 0.483 |
MOD_Plk_1 | 656 | 662 | PF00069 | 0.522 |
MOD_Plk_2-3 | 587 | 593 | PF00069 | 0.451 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.463 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.418 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.425 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.435 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.491 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.537 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.405 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.366 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.488 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.496 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.505 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.316 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.482 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.472 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.724 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.682 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.429 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 615 | 618 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 642 | 645 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 685 | 687 | PF00400 | 0.681 |
TRG_NLS_MonoExtN_4 | 144 | 149 | PF00514 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 273 | 277 | PF00026 | 0.187 |
TRG_Pf-PMV_PEXEL_1 | 305 | 310 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I458 | Leptomonas seymouri | 75% | 100% |
A0A0N1I5R1 | Leptomonas seymouri | 22% | 88% |
A0A0S4IX79 | Bodo saltans | 24% | 96% |
A0A0S4JPF4 | Bodo saltans | 39% | 100% |
A0A1X0P7J3 | Trypanosomatidae | 57% | 100% |
A0A3Q8ID91 | Leishmania donovani | 26% | 100% |
A0A3Q8IF94 | Leishmania donovani | 25% | 100% |
A0A3Q8IG57 | Leishmania donovani | 94% | 90% |
A0A3S7WR01 | Leishmania donovani | 23% | 90% |
A4HGR1 | Leishmania braziliensis | 27% | 100% |
A4HK20 | Leishmania braziliensis | 25% | 100% |
A4HPB9 | Leishmania braziliensis | 87% | 98% |
A4HUC1 | Leishmania infantum | 23% | 90% |
A4I3T6 | Leishmania infantum | 26% | 100% |
A4I7K4 | Leishmania infantum | 25% | 100% |
A4ICF9 | Leishmania infantum | 95% | 100% |
D0A3C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AN20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 95% |
E9AT30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q5P5 | Leishmania major | 25% | 100% |
Q4Q858 | Leishmania major | 26% | 100% |
V5D8J9 | Trypanosoma cruzi | 57% | 100% |