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:0005634 | nucleus | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0032993 | protein-DNA complex | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097550 | transcription preinitiation complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WYT5
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0022607 | cellular component assembly | 4 | 9 |
GO:0043933 | protein-containing complex organization | 4 | 9 |
GO:0065003 | protein-containing complex assembly | 5 | 9 |
GO:0065004 | protein-DNA complex assembly | 6 | 9 |
GO:0070897 | transcription preinitiation complex assembly | 7 | 9 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006352 | DNA-templated transcription initiation | 6 | 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:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 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 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 9 |
GO:0005515 | protein binding | 2 | 9 |
GO:0008134 | transcription factor binding | 3 | 9 |
GO:0017025 | TBP-class protein binding | 5 | 9 |
GO:0140296 | general transcription initiation factor binding | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.251 |
CLV_PCSK_FUR_1 | 577 | 581 | PF00082 | 0.610 |
CLV_PCSK_FUR_1 | 612 | 616 | PF00082 | 0.536 |
CLV_PCSK_FUR_1 | 649 | 653 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 257 | 259 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 628 | 630 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 648 | 650 | PF00082 | 0.587 |
CLV_PCSK_PC7_1 | 388 | 394 | PF00082 | 0.607 |
CLV_PCSK_PC7_1 | 645 | 651 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.275 |
CLV_Separin_Metazoa | 377 | 381 | PF03568 | 0.398 |
DEG_APCC_DBOX_1 | 566 | 574 | PF00400 | 0.604 |
DEG_SCF_FBW7_2 | 344 | 349 | PF00400 | 0.573 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.456 |
DOC_CKS1_1 | 547 | 552 | PF01111 | 0.675 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 612 | 622 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 671 | 680 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 561 | 570 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 614 | 622 | PF00069 | 0.581 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 588 | 591 | PF13499 | 0.602 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 258 | 266 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 292 | 299 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 477 | 486 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 617 | 623 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 631 | 638 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 649 | 655 | PF00244 | 0.610 |
LIG_AP2alpha_2 | 554 | 556 | PF02296 | 0.630 |
LIG_APCC_ABBA_1 | 620 | 625 | PF00400 | 0.587 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.579 |
LIG_BIR_III_4 | 402 | 406 | PF00653 | 0.602 |
LIG_BIR_III_4 | 507 | 511 | PF00653 | 0.613 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 8 | 12 | PF00533 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 329 | 334 | PF00928 | 0.403 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.517 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.382 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.450 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.437 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.490 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.583 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.614 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.513 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.499 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.357 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.584 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.512 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.814 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.499 |
LIG_FHA_2 | 662 | 668 | PF00498 | 0.506 |
LIG_IRF3_LxIS_1 | 92 | 99 | PF10401 | 0.475 |
LIG_LIR_Gen_1 | 146 | 155 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 480 | 491 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 586 | 593 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 586 | 590 | PF02991 | 0.577 |
LIG_OCRL_FandH_1 | 333 | 345 | PF00620 | 0.461 |
LIG_REV1ctd_RIR_1 | 556 | 565 | PF16727 | 0.573 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.492 |
LIG_SH2_GRB2like | 452 | 455 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 311 | 315 | PF00017 | 0.384 |
LIG_SH2_SRC | 276 | 279 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.563 |
LIG_SH3_2 | 322 | 327 | PF14604 | 0.452 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.450 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.458 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.651 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.698 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.559 |
LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.607 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.518 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.545 |
LIG_TRAF2_1 | 569 | 572 | PF00917 | 0.535 |
LIG_TRAF2_1 | 634 | 637 | PF00917 | 0.530 |
LIG_TRFH_1 | 34 | 38 | PF08558 | 0.573 |
LIG_TYR_ITIM | 309 | 314 | PF00017 | 0.486 |
LIG_TYR_ITIM | 602 | 607 | PF00017 | 0.617 |
LIG_UBA3_1 | 158 | 163 | PF00899 | 0.464 |
LIG_UBA3_1 | 309 | 318 | PF00899 | 0.492 |
LIG_UBA3_1 | 364 | 371 | PF00899 | 0.458 |
MOD_CDK_SPxK_1 | 321 | 327 | PF00069 | 0.453 |
MOD_CDK_SPxxK_3 | 262 | 269 | PF00069 | 0.585 |
MOD_CDK_SPxxK_3 | 546 | 553 | PF00069 | 0.550 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.309 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.484 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.528 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.524 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.751 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.639 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.574 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.517 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.377 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.595 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.473 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.565 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.547 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.814 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.502 |
MOD_CK2_1 | 661 | 667 | PF00069 | 0.619 |
MOD_Cter_Amidation | 216 | 219 | PF01082 | 0.251 |
MOD_Cter_Amidation | 255 | 258 | PF01082 | 0.299 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.251 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.496 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.427 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.574 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.801 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.588 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.739 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.496 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.491 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.534 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.560 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.425 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.706 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.575 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.721 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.616 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.488 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.611 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.582 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.562 |
MOD_N-GLC_1 | 529 | 534 | PF02516 | 0.667 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.471 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.582 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.299 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.499 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.543 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.499 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.706 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.566 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.665 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.541 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.417 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.464 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.532 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.685 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.755 |
MOD_PIKK_1 | 678 | 684 | PF00454 | 0.490 |
MOD_PK_1 | 650 | 656 | PF00069 | 0.638 |
MOD_PKA_1 | 257 | 263 | PF00069 | 0.499 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.580 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.431 |
MOD_PKA_1 | 650 | 656 | PF00069 | 0.669 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.497 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.395 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.516 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.450 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.450 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.614 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.528 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.602 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.510 |
MOD_PKB_1 | 629 | 637 | PF00069 | 0.619 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.496 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.674 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.611 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.586 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.595 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.469 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.584 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.517 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.517 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.425 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.487 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.496 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.450 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.597 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.457 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.490 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.421 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.647 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.576 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.701 |
MOD_SUMO_for_1 | 382 | 385 | PF00179 | 0.461 |
MOD_SUMO_for_1 | 391 | 394 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 312 | 320 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 348 | 356 | PF00179 | 0.486 |
TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_1 | 482 | 487 | PF01217 | 0.583 |
TRG_DiLeu_BaEn_4 | 348 | 354 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 636 | 642 | PF01217 | 0.529 |
TRG_DiLeu_LyEn_5 | 385 | 390 | PF01217 | 0.524 |
TRG_DiLeu_LyEn_5 | 482 | 487 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 612 | 615 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 649 | 652 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 670 | 673 | PF00400 | 0.510 |
TRG_NES_CRM1_1 | 88 | 101 | PF08389 | 0.517 |
TRG_NLS_Bipartite_1 | 614 | 632 | PF00514 | 0.567 |
TRG_NLS_MonoCore_2 | 647 | 652 | PF00514 | 0.542 |
TRG_NLS_MonoExtC_3 | 647 | 652 | PF00514 | 0.588 |
TRG_NLS_MonoExtN_4 | 626 | 632 | PF00514 | 0.626 |
TRG_NLS_MonoExtN_4 | 645 | 652 | PF00514 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.251 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM92 | Leptomonas seymouri | 72% | 100% |
A4HDY6 | Leishmania braziliensis | 86% | 99% |
A4I187 | Leishmania infantum | 100% | 100% |
D0A5H2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AXC1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4QA51 | Leishmania major | 95% | 100% |
V5DPA1 | Trypanosoma cruzi | 49% | 100% |