Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 16 |
GO:0099080 | supramolecular complex | 2 | 16 |
GO:0099081 | supramolecular polymer | 3 | 16 |
GO:0099512 | supramolecular fiber | 4 | 16 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0000922 | spindle pole | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005819 | spindle | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9API5
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 16 |
GO:0007018 | microtubule-based movement | 3 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007019 | microtubule depolymerization | 5 | 2 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 2 |
GO:0032984 | protein-containing complex disassembly | 5 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051261 | protein depolymerization | 6 | 2 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003774 | cytoskeletal motor activity | 1 | 16 |
GO:0003777 | microtubule motor activity | 2 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005515 | protein binding | 2 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0008017 | microtubule binding | 5 | 16 |
GO:0008092 | cytoskeletal protein binding | 3 | 16 |
GO:0015631 | tubulin binding | 4 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.287 |
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.302 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.238 |
CLV_C14_Caspase3-7 | 642 | 646 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 702 | 704 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.480 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 702 | 704 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 708 | 710 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.310 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.586 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.336 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.366 |
DEG_SCF_FBW7_1 | 616 | 621 | PF00400 | 0.624 |
DEG_SPOP_SBC_1 | 554 | 558 | PF00917 | 0.650 |
DOC_AGCK_PIF_1 | 411 | 416 | PF00069 | 0.238 |
DOC_ANK_TNKS_1 | 177 | 184 | PF00023 | 0.704 |
DOC_CKS1_1 | 106 | 111 | PF01111 | 0.691 |
DOC_CKS1_1 | 569 | 574 | PF01111 | 0.581 |
DOC_CKS1_1 | 631 | 636 | PF01111 | 0.698 |
DOC_CYCLIN_RxL_1 | 441 | 451 | PF00134 | 0.277 |
DOC_MAPK_gen_1 | 188 | 198 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 315 | 324 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 51 | 60 | PF00069 | 0.431 |
DOC_MAPK_HePTP_8 | 312 | 324 | PF00069 | 0.256 |
DOC_MAPK_MEF2A_6 | 189 | 198 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 315 | 324 | PF00069 | 0.261 |
DOC_MAPK_MEF2A_6 | 394 | 403 | PF00069 | 0.277 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.268 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.238 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.540 |
DOC_USP7_UBL2_3 | 511 | 515 | PF12436 | 0.399 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.285 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 132 | 141 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 193 | 197 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 245 | 249 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 413 | 417 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 517 | 527 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 593 | 599 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 601 | 608 | PF00244 | 0.691 |
LIG_BRCT_BRCA1_1 | 541 | 545 | PF00533 | 0.555 |
LIG_EH1_1 | 40 | 48 | PF00400 | 0.502 |
LIG_EH1_1 | 659 | 667 | PF00400 | 0.507 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.403 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.262 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.239 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.256 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.277 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.277 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.572 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.577 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.238 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.238 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.324 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.248 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.409 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.287 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.277 |
LIG_LIR_Apic_2 | 612 | 616 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 210 | 220 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 247 | 252 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 292 | 299 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 311 | 320 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 415 | 420 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 415 | 419 | PF02991 | 0.270 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.277 |
LIG_NRBOX | 4 | 10 | PF00104 | 0.378 |
LIG_NRP_CendR_1 | 723 | 724 | PF00754 | 0.576 |
LIG_Pex14_2 | 410 | 414 | PF04695 | 0.238 |
LIG_Rb_LxCxE_1 | 340 | 361 | PF01857 | 0.238 |
LIG_REV1ctd_RIR_1 | 408 | 417 | PF16727 | 0.238 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.238 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.238 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.256 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.386 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.362 |
LIG_SH2_CRK | 613 | 617 | PF00017 | 0.667 |
LIG_SH2_SRC | 262 | 265 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.238 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.238 |
LIG_SH2_STAP1 | 506 | 510 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 714 | 718 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 689 | 692 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.474 |
LIG_SH3_2 | 100 | 105 | PF14604 | 0.665 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.670 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.619 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.628 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.619 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 192 | 198 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 224 | 230 | PF11976 | 0.282 |
LIG_SxIP_EBH_1 | 99 | 112 | PF03271 | 0.458 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.512 |
LIG_TRAF2_2 | 231 | 236 | PF00917 | 0.238 |
LIG_UBA3_1 | 225 | 234 | PF00899 | 0.267 |
LIG_UBA3_1 | 446 | 450 | PF00899 | 0.277 |
LIG_UBA3_1 | 54 | 62 | PF00899 | 0.352 |
LIG_UBA3_1 | 665 | 670 | PF00899 | 0.379 |
LIG_WRC_WIRS_1 | 577 | 582 | PF05994 | 0.686 |
MOD_CDC14_SPxK_1 | 607 | 610 | PF00782 | 0.702 |
MOD_CDK_SPxK_1 | 105 | 111 | PF00069 | 0.651 |
MOD_CDK_SPxK_1 | 604 | 610 | PF00069 | 0.701 |
MOD_CDK_SPxxK_3 | 105 | 112 | PF00069 | 0.623 |
MOD_CDK_SPxxK_3 | 170 | 177 | PF00069 | 0.617 |
MOD_CDK_SPxxK_3 | 568 | 575 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 604 | 611 | PF00069 | 0.703 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.607 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.488 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.277 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.292 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.261 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.256 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.277 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.238 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.639 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.611 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.699 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.599 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.604 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.512 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.583 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.408 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.237 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.297 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.277 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.600 |
MOD_Cter_Amidation | 175 | 178 | PF01082 | 0.715 |
MOD_Cter_Amidation | 721 | 724 | PF01082 | 0.518 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.653 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.282 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.238 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.603 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.577 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.630 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.664 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.648 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.504 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.593 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.420 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.548 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.589 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.238 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.259 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.547 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.604 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.736 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.617 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.609 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.633 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.641 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.666 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.712 |
MOD_LATS_1 | 620 | 626 | PF00433 | 0.594 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.277 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.371 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.277 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.238 |
MOD_N-GLC_1 | 594 | 599 | PF02516 | 0.599 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.564 |
MOD_N-GLC_2 | 355 | 357 | PF02516 | 0.241 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.442 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.305 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.238 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.287 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.303 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.669 |
MOD_NEK2_2 | 277 | 282 | PF00069 | 0.303 |
MOD_NEK2_2 | 376 | 381 | PF00069 | 0.238 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.599 |
MOD_PIKK_1 | 671 | 677 | PF00454 | 0.535 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.449 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.704 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.434 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.712 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.391 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.259 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.255 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.411 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.268 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.277 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.277 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.654 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.590 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.383 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.368 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.371 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.283 |
MOD_Plk_1 | 497 | 503 | PF00069 | 0.277 |
MOD_Plk_1 | 588 | 594 | PF00069 | 0.714 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.670 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.495 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.553 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.791 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.277 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.294 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.292 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.277 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.620 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.613 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.285 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.604 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.623 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.526 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.591 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.603 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.555 |
MOD_SUMO_for_1 | 669 | 672 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 249 | 257 | PF00179 | 0.283 |
TRG_DiLeu_BaEn_1 | 302 | 307 | PF01217 | 0.238 |
TRG_DiLeu_BaEn_1 | 650 | 655 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_2 | 55 | 61 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_3 | 650 | 656 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.280 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.260 |
TRG_ER_diArg_1 | 691 | 693 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 701 | 703 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 707 | 709 | PF00400 | 0.425 |
TRG_NLS_Bipartite_1 | 188 | 203 | PF00514 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.277 |
TRG_Pf-PMV_PEXEL_1 | 52 | 56 | PF00026 | 0.348 |
TRG_Pf-PMV_PEXEL_1 | 702 | 706 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 709 | 713 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P6 | Leptomonas seymouri | 46% | 100% |
A0A0N1PAZ2 | Leptomonas seymouri | 81% | 97% |
A0A0N1PDD6 | Leptomonas seymouri | 29% | 95% |
A0A1X0NL76 | Trypanosomatidae | 65% | 100% |
A0A3S5H4S8 | Leishmania donovani | 45% | 100% |
A0A3S7WST0 | Leishmania donovani | 98% | 99% |
A0A3S7X9Y1 | Leishmania donovani | 35% | 100% |
A0A422P055 | Trypanosoma rangeli | 36% | 100% |
A0A422P4C5 | Trypanosoma rangeli | 63% | 100% |
A4H7F1 | Leishmania braziliensis | 93% | 100% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HND6 | Leishmania braziliensis | 34% | 100% |
A4HRC5 | Leishmania infantum | 45% | 100% |
A4HSA6 | Leishmania infantum | 30% | 100% |
A4HVT9 | Leishmania infantum | 98% | 99% |
A4I9W6 | Leishmania infantum | 27% | 68% |
A4IC09 | Leishmania infantum | 35% | 100% |
B9EY52 | Oryza sativa subsp. japonica | 41% | 100% |
B9FMJ3 | Oryza sativa subsp. japonica | 38% | 88% |
C9ZXH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A6E6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
E9ABZ2 | Leishmania major | 46% | 100% |
E9AFU7 | Leishmania major | 34% | 100% |
E9AJ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9B4X8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 67% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q4QFZ3 | Leishmania major | 97% | 100% |
Q940B8 | Arabidopsis thaliana | 40% | 91% |
Q940Y8 | Arabidopsis thaliana | 42% | 100% |
V5BHI2 | Trypanosoma cruzi | 65% | 100% |
V5DSJ9 | Trypanosoma cruzi | 42% | 100% |