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. | yes | 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: Q4QFZ3
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 3 |
GO:0006996 | organelle organization | 4 | 3 |
GO:0007010 | cytoskeleton organization | 5 | 3 |
GO:0007017 | microtubule-based process | 2 | 16 |
GO:0007018 | microtubule-based movement | 3 | 16 |
GO:0007019 | microtubule depolymerization | 5 | 3 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0022411 | cellular component disassembly | 4 | 3 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 3 |
GO:0032984 | protein-containing complex disassembly | 5 | 3 |
GO:0043933 | protein-containing complex organization | 4 | 3 |
GO:0051261 | protein depolymerization | 6 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
GO:0097435 | supramolecular fiber organization | 4 | 3 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
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 | 211 | 215 | PF00656 | 0.357 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.338 |
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.297 |
CLV_C14_Caspase3-7 | 590 | 594 | PF00656 | 0.713 |
CLV_C14_Caspase3-7 | 646 | 650 | PF00656 | 0.654 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 695 | 697 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 695 | 697 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 712 | 714 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.817 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.393 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.425 |
DEG_SCF_FBW7_1 | 620 | 625 | PF00400 | 0.684 |
DEG_SPOP_SBC_1 | 558 | 562 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 606 | 610 | PF00917 | 0.717 |
DOC_AGCK_PIF_1 | 415 | 420 | PF00069 | 0.297 |
DOC_ANK_TNKS_1 | 181 | 188 | PF00023 | 0.762 |
DOC_CKS1_1 | 110 | 115 | PF01111 | 0.755 |
DOC_CKS1_1 | 573 | 578 | PF01111 | 0.639 |
DOC_CKS1_1 | 635 | 640 | PF01111 | 0.753 |
DOC_CYCLIN_RxL_1 | 445 | 455 | PF00134 | 0.338 |
DOC_MAPK_gen_1 | 192 | 202 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 302 | 310 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 51 | 60 | PF00069 | 0.489 |
DOC_MAPK_HePTP_8 | 316 | 328 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 193 | 202 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.338 |
DOC_PP2B_LxvP_1 | 97 | 100 | PF13499 | 0.528 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.594 |
DOC_USP7_UBL2_3 | 515 | 519 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 136 | 145 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 197 | 201 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 249 | 253 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 417 | 421 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 597 | 603 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 605 | 612 | PF00244 | 0.749 |
LIG_BRCT_BRCA1_1 | 545 | 549 | PF00533 | 0.626 |
LIG_EH1_1 | 40 | 48 | PF00400 | 0.557 |
LIG_EH1_1 | 663 | 671 | PF00400 | 0.561 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.444 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.325 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.285 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.316 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.338 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.338 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.635 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.758 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.297 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.297 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.383 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.307 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.429 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.338 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.155 |
LIG_LIR_Apic_2 | 616 | 620 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 214 | 224 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 251 | 256 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 296 | 303 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 315 | 324 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 419 | 424 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 419 | 423 | PF02991 | 0.331 |
LIG_NRBOX | 337 | 343 | PF00104 | 0.338 |
LIG_NRBOX | 4 | 10 | PF00104 | 0.440 |
LIG_NRP_CendR_1 | 727 | 728 | PF00754 | 0.635 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.297 |
LIG_Rb_LxCxE_1 | 344 | 365 | PF01857 | 0.297 |
LIG_REV1ctd_RIR_1 | 412 | 421 | PF16727 | 0.297 |
LIG_SH2_CRK | 217 | 221 | PF00017 | 0.297 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.297 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.316 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.425 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.420 |
LIG_SH2_CRK | 617 | 621 | PF00017 | 0.717 |
LIG_SH2_SRC | 266 | 269 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 510 | 514 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 718 | 722 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 693 | 696 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 718 | 721 | PF00017 | 0.492 |
LIG_SH3_2 | 104 | 109 | PF14604 | 0.678 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.632 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.715 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.676 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.688 |
LIG_SUMO_SIM_anti_2 | 196 | 202 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 228 | 234 | PF11976 | 0.342 |
LIG_TRAF2_1 | 526 | 529 | PF00917 | 0.579 |
LIG_TRAF2_2 | 235 | 240 | PF00917 | 0.297 |
LIG_UBA3_1 | 229 | 238 | PF00899 | 0.325 |
LIG_UBA3_1 | 450 | 454 | PF00899 | 0.338 |
LIG_UBA3_1 | 54 | 62 | PF00899 | 0.410 |
LIG_UBA3_1 | 669 | 674 | PF00899 | 0.434 |
LIG_WRC_WIRS_1 | 581 | 586 | PF05994 | 0.743 |
MOD_CDC14_SPxK_1 | 611 | 614 | PF00782 | 0.760 |
MOD_CDK_SPxK_1 | 109 | 115 | PF00069 | 0.720 |
MOD_CDK_SPxK_1 | 608 | 614 | PF00069 | 0.758 |
MOD_CDK_SPxxK_3 | 109 | 116 | PF00069 | 0.663 |
MOD_CDK_SPxxK_3 | 174 | 181 | PF00069 | 0.677 |
MOD_CDK_SPxxK_3 | 572 | 579 | PF00069 | 0.624 |
MOD_CDK_SPxxK_3 | 608 | 615 | PF00069 | 0.760 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.666 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.534 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.336 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.335 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.322 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.316 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.338 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.297 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.692 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.669 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.727 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.612 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.661 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.573 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.668 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.644 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.500 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.296 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.355 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.338 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.657 |
MOD_Cter_Amidation | 179 | 182 | PF01082 | 0.773 |
MOD_Cter_Amidation | 725 | 728 | PF01082 | 0.576 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.342 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.297 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.653 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.653 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.725 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.709 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.564 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.656 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.479 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.592 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.656 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.297 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.297 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.609 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.663 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.756 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.479 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.561 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.676 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.703 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.773 |
MOD_LATS_1 | 624 | 630 | PF00433 | 0.659 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.303 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.425 |
MOD_N-GLC_1 | 446 | 451 | PF02516 | 0.338 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.297 |
MOD_N-GLC_1 | 598 | 603 | PF02516 | 0.665 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.622 |
MOD_N-GLC_2 | 359 | 361 | PF02516 | 0.297 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.486 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.352 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.297 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.338 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.338 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.730 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.363 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.297 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.552 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.655 |
MOD_PIKK_1 | 675 | 681 | PF00454 | 0.590 |
MOD_PIKK_1 | 700 | 706 | PF00454 | 0.504 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.527 |
MOD_PKA_1 | 181 | 187 | PF00069 | 0.763 |
MOD_PKA_1 | 193 | 199 | PF00069 | 0.498 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.770 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.449 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.297 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.297 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.459 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.328 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.422 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.338 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.646 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.439 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.405 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.425 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.338 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.338 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.760 |
MOD_Plk_1 | 640 | 646 | PF00069 | 0.730 |
MOD_Plk_1 | 675 | 681 | PF00069 | 0.555 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.610 |
MOD_Plk_2-3 | 144 | 150 | PF00069 | 0.625 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.338 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.347 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.354 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.338 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.662 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.672 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.338 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.662 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.686 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.581 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.626 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.664 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.625 |
MOD_SUMO_for_1 | 673 | 676 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 253 | 261 | PF00179 | 0.344 |
TRG_DiLeu_BaEn_1 | 306 | 311 | PF01217 | 0.297 |
TRG_DiLeu_BaEn_1 | 654 | 659 | PF01217 | 0.586 |
TRG_DiLeu_BaEn_2 | 55 | 61 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_3 | 654 | 660 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.341 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 695 | 697 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 705 | 707 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 711 | 713 | PF00400 | 0.486 |
TRG_NLS_Bipartite_1 | 192 | 207 | PF00514 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 458 | 462 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 52 | 56 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 706 | 710 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 713 | 717 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P6 | Leptomonas seymouri | 47% | 100% |
A0A0N1PAZ2 | Leptomonas seymouri | 81% | 97% |
A0A0N1PDD6 | Leptomonas seymouri | 29% | 96% |
A0A1X0NL76 | Trypanosomatidae | 66% | 100% |
A0A3S5H4S8 | Leishmania donovani | 46% | 100% |
A0A3S7WST0 | Leishmania donovani | 98% | 100% |
A0A422P4C5 | Trypanosoma rangeli | 64% | 100% |
A4H7F1 | Leishmania braziliensis | 93% | 100% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HRC5 | Leishmania infantum | 46% | 100% |
A4HSA6 | Leishmania infantum | 30% | 100% |
A4HVT9 | Leishmania infantum | 98% | 100% |
A4I9W6 | Leishmania infantum | 27% | 68% |
B9EY52 | Oryza sativa subsp. japonica | 42% | 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) | 64% | 100% |
E9ABZ2 | Leishmania major | 46% | 100% |
E9AJ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9API5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B4X8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 67% |
Q940B8 | Arabidopsis thaliana | 40% | 92% |
Q940Y8 | Arabidopsis thaliana | 42% | 100% |
V5BHI2 | Trypanosoma cruzi | 66% | 100% |
V5BMP0 | Trypanosoma cruzi | 29% | 94% |