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: 10 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005874 | microtubule | 6 | 11 |
GO:0005929 | cilium | 4 | 2 |
GO:0005930 | axoneme | 2 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0097542 | ciliary tip | 2 | 2 |
GO:0099080 | supramolecular complex | 2 | 11 |
GO:0099081 | supramolecular polymer | 3 | 11 |
GO:0099512 | supramolecular fiber | 4 | 11 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: Q4QGE1
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0007018 | microtubule-based movement | 3 | 11 |
GO:0007019 | microtubule depolymerization | 5 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010938 | cytoplasmic microtubule depolymerization | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0030031 | cell projection assembly | 5 | 2 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 2 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 2 |
GO:0032984 | protein-containing complex disassembly | 5 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0051261 | protein depolymerization | 6 | 2 |
GO:0060271 | cilium assembly | 6 | 2 |
GO:0060404 | axonemal microtubule depolymerization | 6 | 2 |
GO:0061523 | cilium disassembly | 6 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 2 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 2 |
GO:1903008 | organelle disassembly | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003774 | cytoskeletal motor activity | 1 | 11 |
GO:0003777 | microtubule motor activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008017 | microtubule binding | 5 | 11 |
GO:0008092 | cytoskeletal protein binding | 3 | 11 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0015631 | tubulin binding | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 505 | 509 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 708 | 710 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 506 | 508 | PF00082 | 0.581 |
CLV_PCSK_PC7_1 | 382 | 388 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.627 |
DEG_APCC_DBOX_1 | 140 | 148 | PF00400 | 0.369 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.681 |
DEG_SCF_FBW7_1 | 524 | 530 | PF00400 | 0.663 |
DEG_SCF_FBW7_2 | 75 | 82 | PF00400 | 0.322 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.259 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.771 |
DOC_CKS1_1 | 524 | 529 | PF01111 | 0.668 |
DOC_CYCLIN_RxL_1 | 283 | 293 | PF00134 | 0.304 |
DOC_CYCLIN_RxL_1 | 477 | 487 | PF00134 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 355 | 361 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 230 | 240 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 301 | 307 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.304 |
DOC_PP1_RVXF_1 | 253 | 259 | PF00149 | 0.437 |
DOC_PP2B_PxIxI_1 | 32 | 38 | PF00149 | 0.470 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.822 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.730 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.322 |
LIG_14-3-3_CanoR_1 | 13 | 21 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 230 | 240 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 255 | 259 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 323 | 332 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 528 | 535 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 572 | 581 | PF00244 | 0.804 |
LIG_14-3-3_CanoR_1 | 611 | 617 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 721 | 725 | PF00244 | 0.550 |
LIG_Actin_WH2_2 | 205 | 222 | PF00022 | 0.322 |
LIG_Actin_WH2_2 | 669 | 685 | PF00022 | 0.642 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.404 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.721 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.370 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.304 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.304 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.777 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.616 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.355 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.487 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.332 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.249 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.664 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.439 |
LIG_FHA_2 | 693 | 699 | PF00498 | 0.514 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.404 |
LIG_GBD_Chelix_1 | 678 | 686 | PF00786 | 0.606 |
LIG_LIR_Apic_2 | 665 | 670 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 257 | 262 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.327 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.304 |
LIG_PCNA_yPIPBox_3 | 699 | 711 | PF02747 | 0.574 |
LIG_RPA_C_Fungi | 606 | 618 | PF08784 | 0.539 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.437 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.382 |
LIG_SH2_CRK | 667 | 671 | PF00017 | 0.562 |
LIG_SH2_GRB2like | 190 | 193 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 88 | 92 | PF00017 | 0.437 |
LIG_SH2_SRC | 190 | 193 | PF00017 | 0.437 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 696 | 700 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.304 |
LIG_SH3_1 | 40 | 46 | PF00018 | 0.469 |
LIG_SH3_2 | 43 | 48 | PF14604 | 0.510 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.636 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.634 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.374 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.317 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.570 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.395 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.564 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.304 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.369 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.369 |
LIG_TRAF2_2 | 452 | 457 | PF00917 | 0.369 |
LIG_UBA3_1 | 288 | 292 | PF00899 | 0.304 |
MOD_CDC14_SPxK_1 | 414 | 417 | PF00782 | 0.481 |
MOD_CDK_SPK_2 | 523 | 528 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 411 | 417 | PF00069 | 0.487 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.737 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.304 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.369 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.335 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.345 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.310 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.769 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.620 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.642 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.725 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.718 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.663 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.661 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.395 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.480 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.224 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.360 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.417 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.578 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.620 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.473 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.509 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.323 |
MOD_GlcNHglycan | 4 | 8 | PF01048 | 0.834 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.735 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.688 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.696 |
MOD_GlcNHglycan | 647 | 652 | PF01048 | 0.646 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.369 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.219 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.628 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.235 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.504 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.368 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.400 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.803 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.517 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.591 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.553 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.625 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.691 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.780 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.794 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.546 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.576 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.304 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.566 |
MOD_N-GLC_1 | 602 | 607 | PF02516 | 0.681 |
MOD_N-GLC_1 | 624 | 629 | PF02516 | 0.606 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.319 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.385 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.412 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.316 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.315 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.615 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.590 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.729 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.516 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.611 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.531 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.438 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.304 |
MOD_PIKK_1 | 540 | 546 | PF00454 | 0.739 |
MOD_PIKK_1 | 624 | 630 | PF00454 | 0.608 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.661 |
MOD_PK_1 | 427 | 433 | PF00069 | 0.429 |
MOD_PKA_1 | 611 | 617 | PF00069 | 0.535 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.846 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.334 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.304 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.304 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.304 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.304 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.684 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.756 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.628 |
MOD_PKA_2 | 720 | 726 | PF00069 | 0.677 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.444 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.326 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.304 |
MOD_Plk_2-3 | 151 | 157 | PF00069 | 0.369 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.321 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.349 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.304 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.621 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.368 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.446 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.608 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.606 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.621 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.304 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.487 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.561 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.322 |
MOD_SUMO_rev_2 | 179 | 186 | PF00179 | 0.382 |
MOD_SUMO_rev_2 | 234 | 242 | PF00179 | 0.347 |
MOD_SUMO_rev_2 | 268 | 277 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 350 | 358 | PF00179 | 0.369 |
MOD_SUMO_rev_2 | 405 | 414 | PF00179 | 0.433 |
MOD_SUMO_rev_2 | 463 | 469 | PF00179 | 0.369 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.304 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 707 | 709 | PF00400 | 0.542 |
TRG_NES_CRM1_1 | 252 | 265 | PF08389 | 0.369 |
TRG_NLS_MonoCore_2 | 40 | 45 | PF00514 | 0.454 |
TRG_NLS_MonoCore_2 | 504 | 509 | PF00514 | 0.563 |
TRG_NLS_MonoExtC_3 | 39 | 44 | PF00514 | 0.418 |
TRG_NLS_MonoExtC_3 | 504 | 510 | PF00514 | 0.488 |
TRG_NLS_MonoExtN_4 | 40 | 45 | PF00514 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 424 | 429 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P647 | Leptomonas seymouri | 69% | 99% |
A0A0S4IJP8 | Bodo saltans | 49% | 97% |
A0A1X0NNY0 | Trypanosomatidae | 63% | 100% |
A0A3S7WS99 | Leishmania donovani | 95% | 100% |
A0A422NBP2 | Trypanosoma rangeli | 63% | 100% |
A4H720 | Leishmania braziliensis | 85% | 100% |
A4HVE9 | Leishmania infantum | 95% | 100% |
D0A6W1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AP47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P46865 | Leishmania chagasi | 27% | 76% |