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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 17 |
GO:0099080 | supramolecular complex | 2 | 17 |
GO:0099081 | supramolecular polymer | 3 | 17 |
GO:0099512 | supramolecular fiber | 4 | 17 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
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: A4H7F1
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 17 |
GO:0007018 | microtubule-based movement | 3 | 17 |
GO:0009987 | cellular process | 1 | 17 |
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 | 17 |
GO:0003774 | cytoskeletal motor activity | 1 | 17 |
GO:0003777 | microtubule motor activity | 2 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005515 | protein binding | 2 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0008017 | microtubule binding | 5 | 17 |
GO:0008092 | cytoskeletal protein binding | 3 | 17 |
GO:0015631 | tubulin binding | 4 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.289 |
CLV_C14_Caspase3-7 | 223 | 227 | PF00656 | 0.306 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.238 |
CLV_C14_Caspase3-7 | 591 | 595 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 696 | 698 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 713 | 715 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 713 | 715 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.311 |
CLV_PCSK_PC1ET2_1 | 615 | 617 | PF00082 | 0.744 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.773 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.401 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.331 |
DEG_SCF_FBW7_1 | 621 | 626 | PF00400 | 0.605 |
DEG_SPOP_SBC_1 | 559 | 563 | PF00917 | 0.654 |
DEG_SPOP_SBC_1 | 82 | 86 | PF00917 | 0.601 |
DOC_AGCK_PIF_1 | 416 | 421 | PF00069 | 0.238 |
DOC_ANK_TNKS_1 | 182 | 189 | PF00023 | 0.707 |
DOC_CKS1_1 | 112 | 117 | PF01111 | 0.682 |
DOC_CKS1_1 | 574 | 579 | PF01111 | 0.580 |
DOC_CKS1_1 | 636 | 641 | PF01111 | 0.689 |
DOC_CYCLIN_RxL_1 | 446 | 456 | PF00134 | 0.280 |
DOC_MAPK_gen_1 | 193 | 203 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 204 | 210 | PF00069 | 0.288 |
DOC_MAPK_gen_1 | 303 | 311 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 320 | 329 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 52 | 61 | PF00069 | 0.426 |
DOC_MAPK_HePTP_8 | 317 | 329 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 194 | 203 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 320 | 329 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 399 | 408 | PF00069 | 0.280 |
DOC_PP4_FxxP_1 | 585 | 588 | PF00568 | 0.585 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.265 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.238 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.561 |
DOC_USP7_UBL2_3 | 516 | 520 | PF12436 | 0.404 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 137 | 146 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 193 | 202 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 250 | 254 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 522 | 532 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 598 | 604 | PF00244 | 0.655 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.558 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.457 |
LIG_EH1_1 | 41 | 49 | PF00400 | 0.497 |
LIG_EH1_1 | 664 | 672 | PF00400 | 0.504 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.568 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.503 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.272 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.241 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.255 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.280 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.280 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.568 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.581 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.242 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.255 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.371 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.280 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.404 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.282 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.288 |
LIG_LIR_Apic_2 | 584 | 588 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 252 | 257 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 316 | 325 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 420 | 425 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 252 | 256 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 316 | 321 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.279 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.280 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.375 |
LIG_NRP_CendR_1 | 728 | 729 | PF00754 | 0.577 |
LIG_Pex14_2 | 415 | 419 | PF04695 | 0.238 |
LIG_Rb_LxCxE_1 | 345 | 366 | PF01857 | 0.238 |
LIG_REV1ctd_RIR_1 | 413 | 422 | PF16727 | 0.238 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.238 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.255 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.274 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.371 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.357 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.238 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 511 | 515 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 719 | 723 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 719 | 722 | PF00017 | 0.431 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.677 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.664 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 196 | 203 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.297 |
LIG_TRAF2_1 | 527 | 530 | PF00917 | 0.539 |
LIG_TRAF2_2 | 236 | 241 | PF00917 | 0.238 |
LIG_UBA3_1 | 230 | 239 | PF00899 | 0.265 |
LIG_UBA3_1 | 451 | 455 | PF00899 | 0.280 |
LIG_UBA3_1 | 55 | 63 | PF00899 | 0.346 |
LIG_UBA3_1 | 670 | 675 | PF00899 | 0.369 |
MOD_CDC14_SPxK_1 | 612 | 615 | PF00782 | 0.687 |
MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.641 |
MOD_CDK_SPxK_1 | 609 | 615 | PF00069 | 0.687 |
MOD_CDK_SPxxK_3 | 111 | 118 | PF00069 | 0.633 |
MOD_CDK_SPxxK_3 | 175 | 182 | PF00069 | 0.608 |
MOD_CDK_SPxxK_3 | 573 | 580 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 609 | 616 | PF00069 | 0.689 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.594 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.476 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.280 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.292 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.263 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.255 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.280 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.238 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.652 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.614 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.673 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.551 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.603 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.520 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.600 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.582 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.415 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.247 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.281 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.280 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.612 |
MOD_Cter_Amidation | 180 | 183 | PF01082 | 0.717 |
MOD_Cter_Amidation | 726 | 729 | PF01082 | 0.518 |
MOD_DYRK1A_RPxSP_1 | 111 | 115 | PF00069 | 0.593 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.473 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.593 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.661 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.614 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.282 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.238 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.615 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.581 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.662 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.651 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.497 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.573 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.415 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.591 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.488 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.238 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.238 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.541 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.609 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.714 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.444 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.502 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.612 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.642 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.679 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.598 |
MOD_LATS_1 | 625 | 631 | PF00433 | 0.586 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.371 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.280 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.238 |
MOD_N-GLC_1 | 599 | 604 | PF02516 | 0.607 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.539 |
MOD_N-GLC_2 | 360 | 362 | PF02516 | 0.238 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.295 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.429 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.280 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.238 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.280 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.280 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.677 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.490 |
MOD_NEK2_2 | 282 | 287 | PF00069 | 0.280 |
MOD_NEK2_2 | 381 | 386 | PF00069 | 0.238 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.402 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.602 |
MOD_PIKK_1 | 676 | 682 | PF00454 | 0.530 |
MOD_PIKK_1 | 701 | 707 | PF00454 | 0.443 |
MOD_PKA_1 | 182 | 188 | PF00069 | 0.709 |
MOD_PKA_1 | 193 | 199 | PF00069 | 0.468 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.719 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.437 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.238 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.238 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.414 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.269 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.280 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.289 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.662 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.595 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.379 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.348 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.371 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.280 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.280 |
MOD_Plk_1 | 593 | 599 | PF00069 | 0.711 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.667 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.491 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.552 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.280 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.299 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.342 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.283 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.632 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.611 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.280 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.603 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.608 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.517 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.559 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.563 |
MOD_SUMO_for_1 | 674 | 677 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 254 | 262 | PF00179 | 0.283 |
TRG_DiLeu_BaEn_1 | 307 | 312 | PF01217 | 0.238 |
TRG_DiLeu_BaEn_1 | 655 | 660 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_2 | 56 | 62 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_3 | 655 | 661 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_4 | 676 | 682 | PF01217 | 0.316 |
TRG_DiLeu_BaLyEn_6 | 270 | 275 | PF01217 | 0.280 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.263 |
TRG_ER_diArg_1 | 696 | 698 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 706 | 708 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 712 | 714 | PF00400 | 0.423 |
TRG_NLS_Bipartite_1 | 193 | 208 | PF00514 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 459 | 463 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 53 | 57 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 707 | 711 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 714 | 718 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P6 | Leptomonas seymouri | 45% | 100% |
A0A0N1PAZ2 | Leptomonas seymouri | 80% | 97% |
A0A0N1PDD6 | Leptomonas seymouri | 28% | 96% |
A0A1X0NL76 | Trypanosomatidae | 64% | 100% |
A0A1X0P0C2 | Trypanosomatidae | 27% | 89% |
A0A3R7MAX4 | Trypanosoma rangeli | 24% | 69% |
A0A3S5H4S8 | Leishmania donovani | 46% | 100% |
A0A3S7WST0 | Leishmania donovani | 93% | 100% |
A0A422P4C5 | Trypanosoma rangeli | 62% | 100% |
A4H337 | Leishmania braziliensis | 45% | 100% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HJ03 | Leishmania braziliensis | 42% | 83% |
A4HRC5 | Leishmania infantum | 46% | 100% |
A4HSA6 | Leishmania infantum | 30% | 100% |
A4HVT9 | Leishmania infantum | 93% | 100% |
A4I9W6 | Leishmania infantum | 26% | 68% |
B9EY52 | Oryza sativa subsp. japonica | 41% | 100% |
B9FMJ3 | Oryza sativa subsp. japonica | 38% | 89% |
C9ZXH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A6E6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9ABZ2 | Leishmania major | 46% | 100% |
E9AJ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9API5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B4X8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 67% |
Q4QFZ3 | Leishmania major | 93% | 100% |
Q940B8 | Arabidopsis thaliana | 40% | 92% |
Q940Y8 | Arabidopsis thaliana | 43% | 100% |
V5BHI2 | Trypanosoma cruzi | 65% | 100% |