Uncharacterized Protein, Uncharacterized
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. | no | yes: 0 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 14 |
GO:0042995 | cell projection | 2 | 14 |
GO:0043226 | organelle | 2 | 14 |
GO:0043227 | membrane-bounded organelle | 3 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 14 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: A4I6T8
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006457 | protein folding | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007021 | tubulin complex assembly | 6 | 1 |
GO:0007023 | post-chaperonin tubulin folding pathway | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0043014 | alpha-tubulin binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.301 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.445 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 765 | 767 | PF00675 | 0.326 |
CLV_PCSK_FUR_1 | 58 | 62 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 787 | 789 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 766 | 770 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.401 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.323 |
DEG_SCF_FBW7_1 | 658 | 665 | PF00400 | 0.275 |
DOC_CDC14_PxL_1 | 372 | 380 | PF14671 | 0.296 |
DOC_CDC14_PxL_1 | 510 | 518 | PF14671 | 0.306 |
DOC_CYCLIN_RxL_1 | 417 | 425 | PF00134 | 0.555 |
DOC_CYCLIN_RxL_1 | 512 | 525 | PF00134 | 0.335 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.653 |
DOC_MAPK_gen_1 | 512 | 521 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 766 | 775 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 512 | 520 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 741 | 750 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 766 | 775 | PF00069 | 0.318 |
DOC_MAPK_NFAT4_5 | 766 | 774 | PF00069 | 0.298 |
DOC_PP1_RVXF_1 | 433 | 440 | PF00149 | 0.304 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.532 |
DOC_PP2B_LxvP_1 | 267 | 270 | PF13499 | 0.476 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.593 |
DOC_USP7_MATH_2 | 177 | 183 | PF00917 | 0.365 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.286 |
DOC_USP7_UBL2_3 | 770 | 774 | PF12436 | 0.467 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 149 | 155 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 36 | 43 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 466 | 471 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 479 | 484 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 638 | 642 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 667 | 675 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 700 | 705 | PF00244 | 0.281 |
LIG_Actin_WH2_2 | 202 | 219 | PF00022 | 0.299 |
LIG_Actin_WH2_2 | 67 | 85 | PF00022 | 0.349 |
LIG_Actin_WH2_2 | 686 | 702 | PF00022 | 0.292 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.529 |
LIG_BIR_III_2 | 50 | 54 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 551 | 555 | PF00533 | 0.327 |
LIG_BRCT_BRCA1_1 | 702 | 706 | PF00533 | 0.322 |
LIG_Clathr_ClatBox_1 | 421 | 425 | PF01394 | 0.290 |
LIG_Clathr_ClatBox_1 | 736 | 740 | PF01394 | 0.290 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.474 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.456 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.322 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.290 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.421 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.573 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.354 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.452 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.435 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.277 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.304 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.312 |
LIG_Integrin_isoDGR_2 | 264 | 266 | PF01839 | 0.494 |
LIG_LIR_Gen_1 | 399 | 410 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 542 | 553 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 703 | 712 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 751 | 759 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 777 | 786 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 552 | 557 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 687 | 693 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 703 | 709 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 751 | 755 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 777 | 783 | PF02991 | 0.372 |
LIG_LRP6_Inhibitor_1 | 429 | 435 | PF00058 | 0.288 |
LIG_MLH1_MIPbox_1 | 551 | 555 | PF16413 | 0.327 |
LIG_NRBOX | 153 | 159 | PF00104 | 0.299 |
LIG_NRBOX | 417 | 423 | PF00104 | 0.301 |
LIG_NRBOX | 515 | 521 | PF00104 | 0.259 |
LIG_PCNA_yPIPBox_3 | 149 | 158 | PF02747 | 0.321 |
LIG_Rb_LxCxE_1 | 159 | 179 | PF01857 | 0.298 |
LIG_SH2_CRK | 752 | 756 | PF00017 | 0.319 |
LIG_SH2_GRB2like | 402 | 405 | PF00017 | 0.282 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.268 |
LIG_SH2_NCK_1 | 780 | 784 | PF00017 | 0.321 |
LIG_SH2_SRC | 780 | 783 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 780 | 784 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 752 | 755 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 785 | 788 | PF00017 | 0.388 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.345 |
LIG_SUMO_SIM_anti_2 | 528 | 533 | PF11976 | 0.463 |
LIG_SUMO_SIM_anti_2 | 674 | 679 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 7 | 14 | PF11976 | 0.440 |
LIG_SUMO_SIM_anti_2 | 806 | 811 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 419 | 425 | PF11976 | 0.540 |
LIG_SUMO_SIM_par_1 | 447 | 454 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 517 | 522 | PF11976 | 0.271 |
LIG_TRAF2_1 | 608 | 611 | PF00917 | 0.307 |
LIG_TYR_ITIM | 400 | 405 | PF00017 | 0.285 |
LIG_TYR_ITIM | 750 | 755 | PF00017 | 0.298 |
LIG_TYR_ITIM | 778 | 783 | PF00017 | 0.296 |
LIG_UBA3_1 | 400 | 407 | PF00899 | 0.293 |
LIG_UBA3_1 | 518 | 523 | PF00899 | 0.333 |
LIG_UBA3_1 | 768 | 774 | PF00899 | 0.303 |
LIG_WRC_WIRS_1 | 205 | 210 | PF05994 | 0.299 |
MOD_CDK_SPxxK_3 | 24 | 31 | PF00069 | 0.546 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.365 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.590 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.443 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.468 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.306 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.360 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.319 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.483 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.696 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.329 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.396 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.298 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.391 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.435 |
MOD_CK2_1 | 716 | 722 | PF00069 | 0.317 |
MOD_Cter_Amidation | 58 | 61 | PF01082 | 0.484 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.567 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.385 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.330 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.362 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.254 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.456 |
MOD_GlcNHglycan | 550 | 554 | PF01048 | 0.336 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.282 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.453 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.302 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.602 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.436 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.310 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.715 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.326 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.384 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.375 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.349 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.375 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.323 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.294 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.337 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.541 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.316 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.393 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.352 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.275 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.422 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.332 |
MOD_LATS_1 | 477 | 483 | PF00433 | 0.253 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.441 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.314 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.258 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.285 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.363 |
MOD_N-GLC_1 | 748 | 753 | PF02516 | 0.416 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.500 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.416 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.475 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.374 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.345 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.322 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.368 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.383 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.314 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.494 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.384 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.338 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.456 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.434 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.413 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.352 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.431 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.424 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.356 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.293 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.384 |
MOD_NEK2_1 | 748 | 753 | PF00069 | 0.303 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.611 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.273 |
MOD_NEK2_2 | 637 | 642 | PF00069 | 0.473 |
MOD_NEK2_2 | 662 | 667 | PF00069 | 0.360 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.477 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.296 |
MOD_PIKK_1 | 707 | 713 | PF00454 | 0.277 |
MOD_PK_1 | 479 | 485 | PF00069 | 0.260 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.481 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.315 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.347 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.491 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.436 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.445 |
MOD_PKB_1 | 32 | 40 | PF00069 | 0.443 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.314 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.291 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.298 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.448 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.347 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.250 |
MOD_Plk_1 | 748 | 754 | PF00069 | 0.405 |
MOD_Plk_1 | 805 | 811 | PF00069 | 0.435 |
MOD_Plk_2-3 | 525 | 531 | PF00069 | 0.287 |
MOD_Plk_2-3 | 605 | 611 | PF00069 | 0.320 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.329 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.428 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.482 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.331 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.310 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.301 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.355 |
MOD_Plk_4 | 805 | 811 | PF00069 | 0.447 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.384 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.558 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.293 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.273 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.506 |
MOD_SUMO_for_1 | 533 | 536 | PF00179 | 0.286 |
MOD_SUMO_rev_2 | 536 | 546 | PF00179 | 0.308 |
TRG_DiLeu_BaEn_2 | 203 | 209 | PF01217 | 0.298 |
TRG_DiLeu_BaLyEn_6 | 417 | 422 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 621 | 626 | PF01217 | 0.300 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 752 | 755 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 780 | 783 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 107 | 110 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 31 | 34 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.408 |
TRG_LysEnd_GGAAcLL_1 | 806 | 811 | PF00790 | 0.434 |
TRG_NES_CRM1_1 | 413 | 425 | PF08389 | 0.291 |
TRG_NES_CRM1_1 | 511 | 525 | PF08389 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 420 | 425 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 607 | 611 | PF00026 | 0.319 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P1M5 | Trypanosomatidae | 26% | 92% |
A0A3Q8IGD6 | Leishmania donovani | 100% | 100% |
A0A3S5ISR4 | Trypanosoma rangeli | 26% | 97% |
A0A451EJK8 | Leishmania donovani | 25% | 76% |
A4H3R1 | Leishmania braziliensis | 23% | 100% |
D0A4F4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 96% |
E9AG21 | Leishmania infantum | 25% | 80% |
E9AIU4 | Leishmania braziliensis | 77% | 100% |
E9B1W0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q6A2 | Leishmania major | 95% | 100% |
Q4QJ80 | Leishmania major | 24% | 100% |
V5BKI3 | Trypanosoma cruzi | 26% | 97% |