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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZK7
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006356 | regulation of transcription by RNA polymerase I | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045943 | positive regulation of transcription by RNA polymerase I | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2000232 | regulation of rRNA processing | 6 | 1 |
GO:2000234 | positive regulation of rRNA processing | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 739 | 743 | PF00656 | 0.613 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 793 | 795 | PF00675 | 0.617 |
CLV_PCSK_FUR_1 | 477 | 481 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 793 | 795 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 476 | 478 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 588 | 590 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 651 | 655 | PF03568 | 0.404 |
DEG_APCC_DBOX_1 | 554 | 562 | PF00400 | 0.394 |
DEG_APCC_DBOX_1 | 660 | 668 | PF00400 | 0.504 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.575 |
DEG_SCF_FBW7_1 | 318 | 323 | PF00400 | 0.353 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.380 |
DOC_CKS1_1 | 503 | 508 | PF01111 | 0.532 |
DOC_CKS1_1 | 516 | 521 | PF01111 | 0.349 |
DOC_MAPK_gen_1 | 249 | 257 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 306 | 312 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 249 | 257 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 371 | 378 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 466 | 474 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 587 | 594 | PF00149 | 0.319 |
DOC_PP2B_LxvP_1 | 689 | 692 | PF13499 | 0.512 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.342 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.672 |
DOC_USP7_MATH_2 | 552 | 558 | PF00917 | 0.288 |
DOC_USP7_UBL2_3 | 26 | 30 | PF12436 | 0.391 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 346 | 356 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 426 | 432 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 479 | 485 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 555 | 559 | PF00244 | 0.298 |
LIG_Actin_WH2_2 | 649 | 667 | PF00022 | 0.515 |
LIG_APCC_ABBA_1 | 253 | 258 | PF00400 | 0.430 |
LIG_BRCT_BRCA1_1 | 532 | 536 | PF00533 | 0.329 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.459 |
LIG_CtBP_PxDLS_1 | 239 | 243 | PF00389 | 0.249 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.578 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.343 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.505 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.378 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.431 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.458 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.395 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.458 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.378 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.357 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.538 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.422 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.452 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.579 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.449 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.400 |
LIG_LIR_Apic_2 | 447 | 451 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 501 | 506 | PF02991 | 0.531 |
LIG_LIR_Apic_2 | 775 | 781 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 554 | 563 | PF02991 | 0.337 |
LIG_LIR_LC3C_4 | 188 | 192 | PF02991 | 0.440 |
LIG_LIR_LC3C_4 | 363 | 367 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 684 | 689 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 732 | 737 | PF02991 | 0.503 |
LIG_MYND_1 | 221 | 225 | PF01753 | 0.491 |
LIG_PCNA_yPIPBox_3 | 135 | 145 | PF02747 | 0.416 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.398 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.360 |
LIG_REV1ctd_RIR_1 | 731 | 739 | PF16727 | 0.666 |
LIG_SH2_CRK | 448 | 452 | PF00017 | 0.419 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.584 |
LIG_SH2_CRK | 778 | 782 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 778 | 782 | PF00017 | 0.432 |
LIG_SH2_PTP2 | 256 | 259 | PF00017 | 0.349 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 391 | 394 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 545 | 548 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 790 | 793 | PF00017 | 0.491 |
LIG_SH3_1 | 84 | 90 | PF00018 | 0.419 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.414 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.558 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.498 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.494 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.341 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.504 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.468 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.497 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.497 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.557 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.350 |
LIG_SUMO_SIM_anti_2 | 292 | 299 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 292 | 299 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 334 | 341 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 467 | 473 | PF11976 | 0.329 |
LIG_TYR_ITIM | 254 | 259 | PF00017 | 0.313 |
LIG_UBA3_1 | 138 | 145 | PF00899 | 0.392 |
LIG_WRC_WIRS_1 | 170 | 175 | PF05994 | 0.446 |
LIG_WRC_WIRS_1 | 431 | 436 | PF05994 | 0.500 |
LIG_WRC_WIRS_1 | 730 | 735 | PF05994 | 0.665 |
LIG_WW_3 | 410 | 414 | PF00397 | 0.480 |
MOD_CDC14_SPxK_1 | 410 | 413 | PF00782 | 0.547 |
MOD_CDC14_SPxK_1 | 463 | 466 | PF00782 | 0.419 |
MOD_CDK_SPxK_1 | 407 | 413 | PF00069 | 0.561 |
MOD_CDK_SPxK_1 | 460 | 466 | PF00069 | 0.422 |
MOD_CDK_SPxxK_3 | 574 | 581 | PF00069 | 0.442 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.524 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.490 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.484 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.388 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.484 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.448 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.281 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.363 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.417 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.487 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.443 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.548 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.390 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.439 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.392 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.689 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.699 |
MOD_Cter_Amidation | 247 | 250 | PF01082 | 0.415 |
MOD_Cter_Amidation | 477 | 480 | PF01082 | 0.420 |
MOD_Cter_Amidation | 586 | 589 | PF01082 | 0.358 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.616 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.532 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.523 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.373 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.416 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.512 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.475 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.384 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.349 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.724 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.687 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.710 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.544 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.497 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.453 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.473 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.448 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.300 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.409 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.498 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.392 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.529 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.348 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.355 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.468 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.767 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.470 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.668 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.635 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.472 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.551 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.434 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.376 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.418 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.480 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.426 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.396 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.329 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.533 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.470 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.533 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.436 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.438 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.385 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.486 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.473 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.468 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.447 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.534 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.375 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.443 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.414 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.528 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.425 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.406 |
MOD_PIKK_1 | 740 | 746 | PF00454 | 0.624 |
MOD_PK_1 | 79 | 85 | PF00069 | 0.473 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.500 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.588 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.430 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.370 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.408 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.514 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.221 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.326 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.408 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.463 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.464 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.476 |
MOD_Plk_1 | 735 | 741 | PF00069 | 0.657 |
MOD_Plk_2-3 | 629 | 635 | PF00069 | 0.447 |
MOD_Plk_2-3 | 736 | 742 | PF00069 | 0.668 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.501 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.374 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.467 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.459 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.460 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.471 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.423 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.431 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.342 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.349 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.622 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.664 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.455 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.726 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.437 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.379 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.452 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.522 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.560 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.378 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.630 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.349 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.481 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.656 |
TRG_AP2beta_CARGO_1 | 200 | 209 | PF09066 | 0.415 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.337 |
TRG_DiLeu_BaEn_1 | 554 | 559 | PF01217 | 0.280 |
TRG_DiLeu_BaEn_1 | 629 | 634 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 219 | 224 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 438 | 443 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 477 | 480 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 571 | 573 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 793 | 795 | PF00400 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.276 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4K6 | Leptomonas seymouri | 68% | 97% |
A0A0S4J855 | Bodo saltans | 34% | 100% |
A0A1X0NYJ9 | Trypanosomatidae | 42% | 100% |
A0A3Q8IGL7 | Leishmania donovani | 93% | 100% |
A0A422P1N8 | Trypanosoma rangeli | 42% | 100% |
A4HG86 | Leishmania braziliensis | 82% | 100% |
A4I3A1 | Leishmania infantum | 92% | 100% |
D0A824 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 95% |
Q4Q8M4 | Leishmania major | 92% | 100% |