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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H466
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0003924 | GTPase activity | 7 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005525 | GTP binding | 5 | 9 |
GO:0016462 | pyrophosphatase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 9 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 9 |
GO:0019001 | guanyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 23 | 27 | PF00656 | 0.370 |
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 523 | 527 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 765 | 767 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 781 | 783 | PF00675 | 0.539 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.554 |
CLV_PCSK_FUR_1 | 705 | 709 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 709 | 711 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 761 | 763 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 765 | 767 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 709 | 711 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 761 | 763 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 705 | 711 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 751 | 755 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 766 | 770 | PF00082 | 0.489 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.342 |
DEG_APCC_DBOX_1 | 683 | 691 | PF00400 | 0.541 |
DEG_APCC_DBOX_1 | 764 | 772 | PF00400 | 0.583 |
DEG_SCF_FBW7_1 | 437 | 444 | PF00400 | 0.421 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.343 |
DOC_CKS1_1 | 406 | 411 | PF01111 | 0.456 |
DOC_CKS1_1 | 742 | 747 | PF01111 | 0.648 |
DOC_CYCLIN_RxL_1 | 212 | 225 | PF00134 | 0.266 |
DOC_CYCLIN_yCln2_LP_2 | 325 | 331 | PF00134 | 0.503 |
DOC_MAPK_gen_1 | 216 | 222 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 321 | 331 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 443 | 452 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 553 | 563 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 765 | 773 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 180 | 188 | PF00069 | 0.294 |
DOC_MAPK_MEF2A_6 | 556 | 563 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 725 | 733 | PF00069 | 0.607 |
DOC_MAPK_NFAT4_5 | 556 | 564 | PF00069 | 0.331 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.329 |
DOC_PP2B_LxvP_1 | 325 | 328 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.421 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.490 |
DOC_USP7_UBL2_3 | 317 | 321 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.565 |
DOC_USP7_UBL2_3 | 556 | 560 | PF12436 | 0.419 |
DOC_USP7_UBL2_3 | 757 | 761 | PF12436 | 0.516 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.387 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 741 | 746 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 47 | 56 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 646 | 651 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 679 | 683 | PF00244 | 0.555 |
LIG_APCC_ABBA_1 | 559 | 564 | PF00400 | 0.332 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.586 |
LIG_BIR_III_2 | 665 | 669 | PF00653 | 0.595 |
LIG_BIR_III_4 | 292 | 296 | PF00653 | 0.465 |
LIG_BIR_III_4 | 622 | 626 | PF00653 | 0.700 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.393 |
LIG_BRCT_BRCA1_2 | 197 | 203 | PF00533 | 0.398 |
LIG_Clathr_ClatBox_1 | 658 | 662 | PF01394 | 0.482 |
LIG_Clathr_ClatBox_1 | 687 | 691 | PF01394 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 169 | 175 | PF00928 | 0.296 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.421 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.409 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.441 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.726 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.343 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.482 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.436 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.370 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.518 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.454 |
LIG_GBD_Chelix_1 | 528 | 536 | PF00786 | 0.429 |
LIG_IBAR_NPY_1 | 333 | 335 | PF08397 | 0.441 |
LIG_Integrin_RGD_1 | 243 | 245 | PF01839 | 0.435 |
LIG_LIR_Gen_1 | 110 | 118 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 380 | 390 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 564 | 574 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 62 | 70 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 633 | 642 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 683 | 692 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 380 | 385 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 564 | 570 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 680 | 685 | PF02991 | 0.563 |
LIG_LYPXL_yS_3 | 417 | 420 | PF13949 | 0.421 |
LIG_Pex14_1 | 236 | 240 | PF04695 | 0.316 |
LIG_REV1ctd_RIR_1 | 247 | 253 | PF16727 | 0.420 |
LIG_RPA_C_Fungi | 364 | 376 | PF08784 | 0.386 |
LIG_RPA_C_Fungi | 691 | 703 | PF08784 | 0.544 |
LIG_SH2_CRK | 672 | 676 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 335 | 339 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 569 | 572 | PF00017 | 0.387 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.486 |
LIG_SH2_SRC | 562 | 565 | PF00017 | 0.339 |
LIG_SH2_SRC | 569 | 572 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 239 | 242 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 588 | 591 | PF00017 | 0.587 |
LIG_SH2_STAT3 | 90 | 93 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.569 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.339 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.500 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.470 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.434 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.439 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.266 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.379 |
LIG_SH3_3 | 746 | 752 | PF00018 | 0.658 |
LIG_SH3_4 | 757 | 764 | PF00018 | 0.584 |
LIG_SUMO_SIM_anti_2 | 182 | 189 | PF11976 | 0.288 |
LIG_SUMO_SIM_anti_2 | 392 | 400 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 734 | 744 | PF11976 | 0.633 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.637 |
LIG_TRAF2_1 | 360 | 363 | PF00917 | 0.537 |
LIG_TRAF2_1 | 609 | 612 | PF00917 | 0.648 |
LIG_TRAF2_1 | 630 | 633 | PF00917 | 0.577 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.526 |
LIG_TRAF2_2 | 387 | 392 | PF00917 | 0.352 |
LIG_TYR_ITIM | 415 | 420 | PF00017 | 0.258 |
LIG_UBA3_1 | 219 | 224 | PF00899 | 0.292 |
LIG_WRC_WIRS_1 | 468 | 473 | PF05994 | 0.348 |
LIG_WW_1 | 573 | 576 | PF00397 | 0.402 |
MOD_CDK_SPxK_1 | 437 | 443 | PF00069 | 0.258 |
MOD_CDK_SPxxK_3 | 159 | 166 | PF00069 | 0.344 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.361 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.407 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.517 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.362 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.479 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.486 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.489 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.434 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.388 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.517 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.597 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.463 |
MOD_Cter_Amidation | 19 | 22 | PF01082 | 0.540 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.403 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.383 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.337 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.343 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.278 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.589 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.629 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.598 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.432 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.416 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.223 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.576 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.453 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.262 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.342 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.486 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.367 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.471 |
MOD_LATS_1 | 313 | 319 | PF00433 | 0.563 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.322 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.382 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.497 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.437 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.425 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.397 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.543 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.263 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.534 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.450 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.431 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.554 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.491 |
MOD_PKA_1 | 708 | 714 | PF00069 | 0.545 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.495 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.436 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.475 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.470 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.569 |
MOD_PKB_1 | 706 | 714 | PF00069 | 0.512 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.549 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.390 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.385 |
MOD_Plk_2-3 | 380 | 386 | PF00069 | 0.446 |
MOD_Plk_2-3 | 524 | 530 | PF00069 | 0.423 |
MOD_Plk_2-3 | 607 | 613 | PF00069 | 0.506 |
MOD_Plk_2-3 | 627 | 633 | PF00069 | 0.598 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.434 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.341 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.407 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.478 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.337 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.569 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.345 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.388 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.258 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.602 |
MOD_ProDKin_1 | 741 | 747 | PF00069 | 0.562 |
MOD_SUMO_for_1 | 353 | 356 | PF00179 | 0.640 |
MOD_SUMO_for_1 | 377 | 380 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 133 | 143 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 154 | 160 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 211 | 218 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 350 | 359 | PF00179 | 0.454 |
TRG_DiLeu_BaEn_1 | 156 | 161 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_2 | 138 | 144 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 528 | 533 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 705 | 708 | PF00400 | 0.510 |
TRG_NES_CRM1_1 | 386 | 400 | PF08389 | 0.281 |
TRG_NLS_MonoExtN_4 | 319 | 325 | PF00514 | 0.439 |
TRG_NLS_MonoExtN_4 | 705 | 712 | PF00514 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 646 | 650 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 766 | 770 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3S3 | Leptomonas seymouri | 74% | 100% |
A0A3S5H5G5 | Leishmania donovani | 86% | 100% |
A0A422NYH3 | Trypanosoma rangeli | 51% | 100% |
A4HSD4 | Leishmania infantum | 86% | 100% |
C9ZPW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 97% |
E9AKC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q2YDM7 | Bos taurus | 34% | 100% |
Q4QJI3 | Leishmania major | 85% | 100% |
Q4R8L2 | Macaca fascicularis | 33% | 100% |
Q6NY89 | Danio rerio | 37% | 100% |
Q9SJF1 | Arabidopsis thaliana | 34% | 100% |