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. | yes | yes: 40 |
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 2 |
GO:0005871 | kinesin complex | 3 | 3 |
GO:0005874 | microtubule | 6 | 5 |
GO:0005875 | microtubule associated complex | 2 | 3 |
GO:0020016 | ciliary pocket | 2 | 2 |
GO:0030863 | cortical cytoskeleton | 6 | 2 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0099080 | supramolecular complex | 2 | 5 |
GO:0099081 | supramolecular polymer | 3 | 5 |
GO:0099512 | supramolecular fiber | 4 | 5 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
Related structures:
AlphaFold database: Q4QEL8
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 17 |
GO:0007018 | microtubule-based movement | 3 | 17 |
GO:0009987 | cellular process | 1 | 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003774 | cytoskeletal motor activity | 1 | 17 |
GO:0003777 | microtubule motor activity | 2 | 17 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 17 |
GO:0005515 | protein binding | 2 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0008017 | microtubule binding | 5 | 17 |
GO:0008092 | cytoskeletal protein binding | 3 | 17 |
GO:0015631 | tubulin binding | 4 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 3 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 3 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 3 |
GO:0016887 | ATP hydrolysis activity | 7 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 3 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.345 |
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 788 | 790 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.463 |
CLV_Separin_Metazoa | 209 | 213 | PF03568 | 0.338 |
DEG_APCC_DBOX_1 | 754 | 762 | PF00400 | 0.463 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.538 |
DOC_CYCLIN_RxL_1 | 246 | 254 | PF00134 | 0.293 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.565 |
DOC_MAPK_RevD_3 | 157 | 172 | PF00069 | 0.305 |
DOC_MIT_MIM_1 | 543 | 551 | PF04212 | 0.438 |
DOC_PP4_FxxP_1 | 115 | 118 | PF00568 | 0.420 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.420 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.318 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 783 | 788 | PF00397 | 0.597 |
LIG_14-3-3_CanoR_1 | 139 | 148 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 225 | 230 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 307 | 312 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 503 | 513 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 547 | 555 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 777 | 785 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 802 | 807 | PF00244 | 0.524 |
LIG_Actin_WH2_2 | 192 | 208 | PF00022 | 0.267 |
LIG_Actin_WH2_2 | 704 | 722 | PF00022 | 0.428 |
LIG_APCC_ABBA_1 | 157 | 162 | PF00400 | 0.342 |
LIG_APCC_ABBAyCdc20_2 | 387 | 393 | PF00400 | 0.409 |
LIG_APCC_ABBAyCdc20_2 | 448 | 454 | PF00400 | 0.530 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.316 |
LIG_Clathr_ClatBox_1 | 229 | 233 | PF01394 | 0.305 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.351 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.370 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.383 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.326 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.326 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.524 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.527 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.579 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.329 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.288 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.310 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.463 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.503 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.603 |
LIG_FHA_2 | 612 | 618 | PF00498 | 0.634 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.518 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.493 |
LIG_FHA_2 | 671 | 677 | PF00498 | 0.450 |
LIG_GBD_Chelix_1 | 526 | 534 | PF00786 | 0.555 |
LIG_KLC1_Yacidic_2 | 158 | 162 | PF13176 | 0.305 |
LIG_LIR_Apic_2 | 113 | 118 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 236 | 241 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 111 | 118 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 197 | 205 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 454 | 462 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 735 | 744 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 78 | 89 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 454 | 458 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 735 | 740 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.322 |
LIG_MYND_1 | 241 | 245 | PF01753 | 0.420 |
LIG_NRBOX | 310 | 316 | PF00104 | 0.342 |
LIG_PCNA_PIPBox_1 | 231 | 240 | PF02747 | 0.316 |
LIG_PCNA_yPIPBox_3 | 301 | 315 | PF02747 | 0.331 |
LIG_PDZ_Class_1 | 802 | 807 | PF00595 | 0.526 |
LIG_Pex14_1 | 379 | 383 | PF04695 | 0.594 |
LIG_Pex14_2 | 53 | 57 | PF04695 | 0.318 |
LIG_PTB_Apo_2 | 131 | 138 | PF02174 | 0.420 |
LIG_SH2_GRB2like | 681 | 684 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 737 | 741 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 16 | 19 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 150 | 154 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 498 | 502 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 681 | 684 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.474 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.329 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 200 | 206 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.234 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 281 | 287 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 325 | 332 | PF11976 | 0.420 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.329 |
LIG_TRAF2_1 | 600 | 603 | PF00917 | 0.620 |
LIG_TRAF2_1 | 614 | 617 | PF00917 | 0.692 |
LIG_TRAF2_1 | 628 | 631 | PF00917 | 0.512 |
LIG_TRAF2_1 | 642 | 645 | PF00917 | 0.486 |
LIG_TRAF2_1 | 75 | 78 | PF00917 | 0.305 |
LIG_UBA3_1 | 753 | 760 | PF00899 | 0.464 |
LIG_WRC_WIRS_1 | 112 | 117 | PF05994 | 0.420 |
LIG_WRC_WIRS_1 | 211 | 216 | PF05994 | 0.305 |
MOD_CDK_SPK_2 | 783 | 788 | PF00069 | 0.568 |
MOD_CDK_SPxK_1 | 783 | 789 | PF00069 | 0.597 |
MOD_CDK_SPxxK_3 | 329 | 336 | PF00069 | 0.287 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.326 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.326 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.337 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.326 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.326 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.330 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.362 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.317 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.424 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.507 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.487 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.549 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.633 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.702 |
MOD_CK2_1 | 625 | 631 | PF00069 | 0.517 |
MOD_CK2_1 | 639 | 645 | PF00069 | 0.476 |
MOD_CK2_1 | 660 | 666 | PF00069 | 0.525 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.468 |
MOD_CK2_1 | 791 | 797 | PF00069 | 0.606 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.326 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.420 |
MOD_GlcNHglycan | 24 | 30 | PF01048 | 0.400 |
MOD_GlcNHglycan | 39 | 43 | PF01048 | 0.402 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.521 |
MOD_GlcNHglycan | 603 | 607 | PF01048 | 0.567 |
MOD_GlcNHglycan | 617 | 621 | PF01048 | 0.506 |
MOD_GlcNHglycan | 631 | 635 | PF01048 | 0.546 |
MOD_GlcNHglycan | 645 | 649 | PF01048 | 0.522 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.473 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.423 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.408 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.370 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.340 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.418 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.316 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.340 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.395 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.335 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.541 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.646 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.518 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.491 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.386 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.606 |
MOD_LATS_1 | 170 | 176 | PF00433 | 0.329 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.326 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.278 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.450 |
MOD_N-GLC_1 | 693 | 698 | PF02516 | 0.463 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.370 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.351 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.344 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.326 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.467 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.603 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.625 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.523 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.495 |
MOD_NEK2_2 | 215 | 220 | PF00069 | 0.400 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.316 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.329 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.365 |
MOD_PK_1 | 766 | 772 | PF00069 | 0.536 |
MOD_PKA_1 | 777 | 783 | PF00069 | 0.595 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.314 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.303 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.605 |
MOD_PKA_2 | 777 | 783 | PF00069 | 0.595 |
MOD_PKB_1 | 295 | 303 | PF00069 | 0.420 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.334 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.291 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.365 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.334 |
MOD_Plk_1 | 611 | 617 | PF00069 | 0.550 |
MOD_Plk_1 | 625 | 631 | PF00069 | 0.517 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.477 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.473 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.462 |
MOD_Plk_1 | 766 | 772 | PF00069 | 0.536 |
MOD_Plk_1 | 796 | 802 | PF00069 | 0.624 |
MOD_Plk_2-3 | 660 | 666 | PF00069 | 0.497 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.367 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.411 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.305 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.362 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.435 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.410 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.386 |
MOD_ProDKin_1 | 783 | 789 | PF00069 | 0.597 |
MOD_SUMO_for_1 | 472 | 475 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 762 | 768 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 797 | 805 | PF00179 | 0.591 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 737 | 740 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.792 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 564 | 567 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 754 | 756 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 787 | 789 | PF00400 | 0.550 |
TRG_NLS_MonoExtN_4 | 48 | 53 | PF00514 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 301 | 305 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 435 | 439 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 503 | 508 | PF00026 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 524 | 529 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 788 | 792 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5H5 | Leptomonas seymouri | 27% | 68% |
A0A0N1IH46 | Leptomonas seymouri | 78% | 100% |
A0A0S4IR67 | Bodo saltans | 28% | 100% |
A0A0S4JMJ1 | Bodo saltans | 28% | 100% |
A0A1X0NDZ3 | Trypanosomatidae | 30% | 72% |
A0A1X0NP27 | Trypanosomatidae | 34% | 100% |
A0A1X0NPH9 | Trypanosomatidae | 26% | 87% |
A0A1X0P0C2 | Trypanosomatidae | 56% | 99% |
A0A3Q8IBS7 | Leishmania donovani | 28% | 100% |
A0A3Q8IDT2 | Leishmania donovani | 94% | 67% |
A0A3Q8IHG6 | Leishmania donovani | 32% | 100% |
A0A3R7KM83 | Trypanosoma rangeli | 29% | 73% |
A0A3R7MU74 | Trypanosoma rangeli | 27% | 72% |
A0A3R7RD86 | Trypanosoma rangeli | 55% | 100% |
A0A3S5H5N6 | Leishmania donovani | 25% | 100% |
A0A3S7WU64 | Leishmania donovani | 89% | 94% |
A0A3S7XBW9 | Leishmania donovani | 23% | 100% |
A4H8S6 | Leishmania braziliensis | 76% | 78% |
A4HIP0 | Leishmania braziliensis | 27% | 68% |
A4HSQ9 | Leishmania infantum | 25% | 100% |
A4HX45 | Leishmania infantum | 91% | 100% |
A4I4V2 | Leishmania infantum | 32% | 100% |
A4I5Y7 | Leishmania infantum | 28% | 68% |
A4IDT7 | Leishmania infantum | 23% | 100% |
C9ZRB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 73% |
D0A9T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 72% |
E9AEA0 | Leishmania major | 32% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AQW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 77% |
E9ATU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 97% |
Q0DV28 | Oryza sativa subsp. japonica | 30% | 85% |
Q2PQA9 | Rattus norvegicus | 27% | 84% |
Q4Q0P7 | Leishmania major | 22% | 100% |
Q4Q6Y4 | Leishmania major | 28% | 68% |
Q4Q7F9 | Leishmania major | 28% | 67% |
Q4Q7S4 | Leishmania major | 27% | 100% |
Q555I8 | Dictyostelium discoideum | 25% | 66% |
Q5R706 | Pongo abelii | 29% | 100% |
Q8S905 | Arabidopsis thaliana | 27% | 83% |
Q8VWI7 | Arabidopsis thaliana | 27% | 93% |
Q9AWM8 | Oryza sativa subsp. japonica | 27% | 85% |
V5B325 | Trypanosoma cruzi | 31% | 97% |
V5BMP0 | Trypanosoma cruzi | 58% | 100% |
V5DNV9 | Trypanosoma cruzi | 27% | 72% |