Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 8 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 30 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 31 |
NetGPI | no | yes: 0, no: 31 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 25 |
GO:0099080 | supramolecular complex | 2 | 25 |
GO:0099081 | supramolecular polymer | 3 | 25 |
GO:0099512 | supramolecular fiber | 4 | 25 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 25 |
GO:0110165 | cellular anatomical entity | 1 | 25 |
GO:0005871 | kinesin complex | 3 | 3 |
GO:0005875 | microtubule associated complex | 2 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0051286 | cell tip | 3 | 3 |
GO:0060187 | cell pole | 2 | 3 |
GO:0097542 | ciliary tip | 2 | 1 |
Related structures:
AlphaFold database: A4HCT2
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 32 |
GO:0007018 | microtubule-based movement | 3 | 32 |
GO:0009987 | cellular process | 1 | 32 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0000902 | cell morphogenesis | 3 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0009653 | anatomical structure morphogenesis | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0030865 | cortical cytoskeleton organization | 6 | 1 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 1 |
GO:0032502 | developmental process | 1 | 1 |
GO:0043622 | cortical microtubule organization | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
GO:0007019 | microtubule depolymerization | 5 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0051261 | protein depolymerization | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 32 |
GO:0003774 | cytoskeletal motor activity | 1 | 32 |
GO:0003777 | microtubule motor activity | 2 | 32 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 32 |
GO:0005515 | protein binding | 2 | 32 |
GO:0005524 | ATP binding | 5 | 32 |
GO:0008017 | microtubule binding | 5 | 32 |
GO:0008092 | cytoskeletal protein binding | 3 | 32 |
GO:0015631 | tubulin binding | 4 | 32 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 32 |
GO:0030554 | adenyl nucleotide binding | 5 | 32 |
GO:0032553 | ribonucleotide binding | 3 | 32 |
GO:0032555 | purine ribonucleotide binding | 4 | 32 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 32 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 32 |
GO:0036094 | small molecule binding | 2 | 32 |
GO:0043167 | ion binding | 2 | 32 |
GO:0043168 | anion binding | 3 | 32 |
GO:0097159 | organic cyclic compound binding | 2 | 32 |
GO:0097367 | carbohydrate derivative binding | 2 | 32 |
GO:0140657 | ATP-dependent activity | 1 | 32 |
GO:1901265 | nucleoside phosphate binding | 3 | 32 |
GO:1901363 | heterocyclic compound binding | 2 | 32 |
GO:0016462 | pyrophosphatase activity | 5 | 3 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 3 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 3 |
GO:0016887 | ATP hydrolysis activity | 7 | 3 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 552 | 556 | PF00656 | 0.492 |
CLV_MEL_PAP_1 | 181 | 187 | PF00089 | 0.285 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 714 | 716 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 384 | 386 | PF00082 | 0.277 |
CLV_PCSK_PC1ET2_1 | 603 | 605 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 634 | 636 | PF00082 | 0.588 |
CLV_PCSK_PC7_1 | 604 | 610 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.299 |
CLV_Separin_Metazoa | 626 | 630 | PF03568 | 0.611 |
CLV_Separin_Metazoa | 702 | 706 | PF03568 | 0.423 |
DEG_APCC_DBOX_1 | 327 | 335 | PF00400 | 0.254 |
DEG_APCC_DBOX_1 | 474 | 482 | PF00400 | 0.553 |
DEG_APCC_DBOX_1 | 576 | 584 | PF00400 | 0.443 |
DOC_MAPK_gen_1 | 211 | 218 | PF00069 | 0.258 |
DOC_MAPK_gen_1 | 440 | 447 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 517 | 525 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 184 | 193 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 211 | 218 | PF00069 | 0.254 |
DOC_MAPK_MEF2A_6 | 389 | 396 | PF00069 | 0.262 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.639 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.323 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.255 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.342 |
LIG_14-3-3_CanoR_1 | 11 | 19 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 204 | 210 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 283 | 290 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 41 | 48 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 414 | 418 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 442 | 448 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 705 | 711 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 219 | 237 | PF00022 | 0.272 |
LIG_APCC_ABBA_1 | 219 | 224 | PF00400 | 0.315 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.349 |
LIG_Clathr_ClatBox_1 | 677 | 681 | PF01394 | 0.370 |
LIG_deltaCOP1_diTrp_1 | 88 | 96 | PF00928 | 0.322 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.288 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.367 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.331 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.327 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.606 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.254 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.282 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.351 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.259 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.507 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.397 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.406 |
LIG_LIR_Apic_2 | 101 | 106 | PF02991 | 0.262 |
LIG_LIR_Apic_2 | 17 | 22 | PF02991 | 0.571 |
LIG_LIR_Apic_2 | 251 | 256 | PF02991 | 0.285 |
LIG_LIR_Apic_2 | 314 | 320 | PF02991 | 0.209 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 160 | 169 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 188 | 197 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 215 | 226 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 528 | 535 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 698 | 707 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 528 | 532 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.630 |
LIG_NRBOX | 400 | 406 | PF00104 | 0.307 |
LIG_NRBOX | 501 | 507 | PF00104 | 0.389 |
LIG_PCNA_yPIPBox_3 | 119 | 133 | PF02747 | 0.278 |
LIG_PTB_Apo_2 | 184 | 191 | PF02174 | 0.272 |
LIG_Rb_pABgroove_1 | 161 | 169 | PF01858 | 0.418 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.335 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.278 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.272 |
LIG_SH2_NCK_1 | 130 | 134 | PF00017 | 0.254 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 597 | 601 | PF00017 | 0.586 |
LIG_SH2_STAT3 | 123 | 126 | PF00017 | 0.302 |
LIG_SH2_STAT3 | 541 | 544 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.255 |
LIG_SH3_1 | 389 | 395 | PF00018 | 0.272 |
LIG_SH3_2 | 392 | 397 | PF14604 | 0.272 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.194 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.247 |
LIG_SUMO_SIM_par_1 | 664 | 670 | PF11976 | 0.660 |
LIG_SUMO_SIM_par_1 | 78 | 85 | PF11976 | 0.249 |
LIG_TRAF2_1 | 487 | 490 | PF00917 | 0.630 |
LIG_TRAF2_1 | 576 | 579 | PF00917 | 0.451 |
LIG_UBA3_1 | 189 | 194 | PF00899 | 0.256 |
LIG_WRC_WIRS_1 | 112 | 117 | PF05994 | 0.285 |
LIG_WRC_WIRS_1 | 319 | 324 | PF05994 | 0.297 |
LIG_WRC_WIRS_1 | 45 | 50 | PF05994 | 0.433 |
MOD_CDK_SPK_2 | 4 | 9 | PF00069 | 0.782 |
MOD_CDK_SPxK_1 | 4 | 10 | PF00069 | 0.718 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.656 |
MOD_CDK_SPxxK_3 | 419 | 426 | PF00069 | 0.272 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.300 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.311 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.241 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.331 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.331 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.410 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.346 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.382 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.474 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.508 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.272 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.679 |
MOD_Cter_Amidation | 382 | 385 | PF01082 | 0.429 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.329 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.309 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.305 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.515 |
MOD_GlcNHglycan | 654 | 658 | PF01048 | 0.626 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.675 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.298 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.249 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.285 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.365 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.334 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.349 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.533 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.367 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.377 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.561 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.306 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.301 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.352 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.337 |
MOD_N-GLC_2 | 146 | 148 | PF02516 | 0.287 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.274 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.346 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.325 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.359 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.322 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.327 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.375 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.617 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.508 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.418 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.328 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.631 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.283 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.400 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.370 |
MOD_PK_1 | 10 | 16 | PF00069 | 0.538 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.583 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.598 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.303 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.325 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.325 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.327 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.409 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.327 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.527 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.530 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.286 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.341 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.345 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.353 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.631 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.288 |
MOD_Plk_2-3 | 584 | 590 | PF00069 | 0.419 |
MOD_Plk_2-3 | 69 | 75 | PF00069 | 0.285 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.317 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.385 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.298 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.350 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.321 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.428 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.371 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.389 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.284 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.256 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.255 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.630 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.342 |
MOD_SUMO_for_1 | 487 | 490 | PF00179 | 0.413 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.312 |
MOD_SUMO_for_1 | 595 | 598 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 308 | 318 | PF00179 | 0.227 |
MOD_SUMO_rev_2 | 573 | 583 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 584 | 592 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 670 | 678 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 72 | 82 | PF00179 | 0.207 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.247 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 607 | 609 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 642 | 644 | PF00400 | 0.451 |
TRG_NES_CRM1_1 | 302 | 314 | PF08389 | 0.297 |
TRG_NLS_MonoExtN_4 | 8 | 13 | PF00514 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 389 | 393 | PF00026 | 0.298 |
TRG_Pf-PMV_PEXEL_1 | 493 | 498 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 634 | 638 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 643 | 647 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 653 | 658 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.251 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A068FIK2 | Gossypium hirsutum | 30% | 70% |
A0A0N1I1K9 | Leptomonas seymouri | 24% | 100% |
A0A0N1IMQ7 | Leptomonas seymouri | 26% | 67% |
A0A0N1PDD6 | Leptomonas seymouri | 74% | 95% |
A0A0S4IR67 | Bodo saltans | 58% | 92% |
A0A0S4J2K1 | Bodo saltans | 32% | 75% |
A0A0S4JRN9 | Bodo saltans | 33% | 100% |
A0A0S4KL43 | Bodo saltans | 26% | 100% |
A0A0S4KM02 | Bodo saltans | 33% | 71% |
A0A1X0NNL3 | Trypanosomatidae | 30% | 70% |
A0A1X0NWZ8 | Trypanosomatidae | 63% | 97% |
A0A3Q8IAZ2 | Leishmania donovani | 82% | 100% |
A0A3Q8IEL2 | Leishmania donovani | 31% | 100% |
A0A3Q8IIF6 | Leishmania donovani | 28% | 67% |
A0A3R7KHX7 | Trypanosoma rangeli | 30% | 97% |
A0A3R7LER1 | Trypanosoma rangeli | 31% | 79% |
A0A3R7NW09 | Trypanosoma rangeli | 29% | 69% |
A0A3S7WY84 | Leishmania donovani | 32% | 100% |
A0A3S7X9Y1 | Leishmania donovani | 25% | 100% |
A0A422NEQ8 | Trypanosoma rangeli | 70% | 95% |
A0A422NMD1 | Trypanosoma rangeli | 24% | 100% |
A4H7S0 | Leishmania braziliensis | 28% | 67% |
A4HAQ7 | Leishmania braziliensis | 32% | 100% |
A4HDC2 | Leishmania braziliensis | 32% | 100% |
A4HND6 | Leishmania braziliensis | 26% | 100% |
A4HQ31 | Leishmania braziliensis | 23% | 100% |
A4HSA6 | Leishmania infantum | 28% | 100% |
A4I0A6 | Leishmania infantum | 82% | 100% |
A4I0Q2 | Leishmania infantum | 32% | 100% |
A4I4V3 | Leishmania infantum | 31% | 100% |
A4I9W6 | Leishmania infantum | 28% | 67% |
A4IC09 | Leishmania infantum | 25% | 100% |
C9ZTV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 81% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 96% |
D0A8T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AEA0 | Leishmania major | 31% | 100% |
E9AEA1 | Leishmania major | 31% | 100% |
E9AFU7 | Leishmania major | 25% | 100% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AW71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9AWQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AXS9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 67% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
F4K4C5 | Arabidopsis thaliana | 28% | 94% |
O59751 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 92% |
Q0WN69 | Arabidopsis thaliana | 30% | 70% |
Q4QAR9 | Leishmania major | 32% | 100% |
Q6H638 | Oryza sativa subsp. japonica | 29% | 81% |
Q9I869 | Xenopus laevis | 28% | 100% |
Q9NF78 | Leishmania major | 82% | 100% |
Q9SCJ4 | Arabidopsis thaliana | 27% | 89% |
V5B325 | Trypanosoma cruzi | 32% | 87% |
V5B6Q5 | Trypanosoma cruzi | 25% | 100% |
V5D733 | Trypanosoma cruzi | 60% | 96% |