Structural Proteins, Kinesin-like
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: 25 |
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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 14 |
GO:0099080 | supramolecular complex | 2 | 14 |
GO:0099081 | supramolecular polymer | 3 | 14 |
GO:0099512 | supramolecular fiber | 4 | 14 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005929 | cilium | 4 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0097542 | ciliary tip | 2 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
Related structures:
AlphaFold database: A4HVE9
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 20 |
GO:0007018 | microtubule-based movement | 3 | 20 |
GO:0009987 | cellular process | 1 | 20 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007019 | microtubule depolymerization | 5 | 1 |
GO:0010938 | cytoplasmic microtubule depolymerization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 1 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0051261 | protein depolymerization | 6 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0060404 | axonemal microtubule depolymerization | 6 | 1 |
GO:0061523 | cilium disassembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
GO:1903008 | organelle disassembly | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 20 |
GO:0003774 | cytoskeletal motor activity | 1 | 20 |
GO:0003777 | microtubule motor activity | 2 | 20 |
GO:0005488 | binding | 1 | 20 |
GO:0005515 | protein binding | 2 | 20 |
GO:0005524 | ATP binding | 5 | 20 |
GO:0008017 | microtubule binding | 5 | 20 |
GO:0008092 | cytoskeletal protein binding | 3 | 20 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0015631 | tubulin binding | 4 | 20 |
GO:0017076 | purine nucleotide binding | 4 | 20 |
GO:0030554 | adenyl nucleotide binding | 5 | 20 |
GO:0032553 | ribonucleotide binding | 3 | 20 |
GO:0032555 | purine ribonucleotide binding | 4 | 20 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 20 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 20 |
GO:0036094 | small molecule binding | 2 | 20 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043168 | anion binding | 3 | 20 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 20 |
GO:0097367 | carbohydrate derivative binding | 2 | 20 |
GO:0140657 | ATP-dependent activity | 1 | 20 |
GO:1901265 | nucleoside phosphate binding | 3 | 20 |
GO:1901363 | heterocyclic compound binding | 2 | 20 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.464 |
CLV_PCSK_FUR_1 | 502 | 506 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 503 | 505 | PF00082 | 0.465 |
CLV_PCSK_PC7_1 | 379 | 385 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.239 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.266 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.594 |
DEG_SCF_FBW7_1 | 521 | 527 | PF00400 | 0.624 |
DEG_SCF_FBW7_2 | 72 | 79 | PF00400 | 0.260 |
DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.793 |
DOC_CKS1_1 | 521 | 526 | PF01111 | 0.626 |
DOC_CYCLIN_RxL_1 | 280 | 290 | PF00134 | 0.246 |
DOC_CYCLIN_RxL_1 | 474 | 484 | PF00134 | 0.470 |
DOC_CYCLIN_yCln2_LP_2 | 352 | 358 | PF00134 | 0.554 |
DOC_MAPK_gen_1 | 227 | 237 | PF00069 | 0.260 |
DOC_MAPK_gen_1 | 298 | 304 | PF00069 | 0.286 |
DOC_MAPK_MEF2A_6 | 230 | 239 | PF00069 | 0.285 |
DOC_MAPK_RevD_3 | 490 | 505 | PF00069 | 0.291 |
DOC_PP1_RVXF_1 | 250 | 256 | PF00149 | 0.373 |
DOC_PP1_SILK_1 | 554 | 559 | PF00149 | 0.515 |
DOC_PP2B_PxIxI_1 | 29 | 35 | PF00149 | 0.390 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.532 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.305 |
LIG_14-3-3_CanoR_1 | 13 | 21 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 227 | 237 | PF00244 | 0.283 |
LIG_14-3-3_CanoR_1 | 252 | 256 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 293 | 298 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 320 | 329 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 525 | 532 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 569 | 578 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 603 | 608 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 718 | 722 | PF00244 | 0.433 |
LIG_Actin_WH2_2 | 202 | 219 | PF00022 | 0.260 |
LIG_Actin_WH2_2 | 666 | 682 | PF00022 | 0.517 |
LIG_BRCT_BRCA1_1 | 616 | 620 | PF00533 | 0.638 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.387 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.674 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.280 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.299 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.321 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.565 |
LIG_FHA_1 | 710 | 716 | PF00498 | 0.527 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.335 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.289 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.277 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.239 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.453 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.412 |
LIG_FHA_2 | 690 | 696 | PF00498 | 0.403 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.313 |
LIG_GBD_Chelix_1 | 675 | 683 | PF00786 | 0.506 |
LIG_LIR_Apic_2 | 662 | 667 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 254 | 259 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 82 | 92 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.302 |
LIG_NRBOX | 169 | 175 | PF00104 | 0.246 |
LIG_PCNA_yPIPBox_3 | 696 | 708 | PF02747 | 0.447 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.373 |
LIG_SH2_CRK | 187 | 191 | PF00017 | 0.313 |
LIG_SH2_CRK | 664 | 668 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 187 | 190 | PF00017 | 0.373 |
LIG_SH2_NCK_1 | 85 | 89 | PF00017 | 0.373 |
LIG_SH2_SRC | 187 | 190 | PF00017 | 0.373 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 693 | 697 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.425 |
LIG_SH3_1 | 37 | 43 | PF00018 | 0.381 |
LIG_SH3_2 | 40 | 45 | PF14604 | 0.417 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.556 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.624 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.304 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.419 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.397 |
LIG_SH3_3 | 654 | 660 | PF00018 | 0.467 |
LIG_SUMO_SIM_par_1 | 284 | 290 | PF11976 | 0.246 |
LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.439 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.266 |
LIG_TRAF2_2 | 449 | 454 | PF00917 | 0.439 |
LIG_UBA3_1 | 285 | 289 | PF00899 | 0.294 |
MOD_CDC14_SPxK_1 | 411 | 414 | PF00782 | 0.339 |
MOD_CDK_SPK_2 | 520 | 525 | PF00069 | 0.630 |
MOD_CDK_SPK_2 | 604 | 609 | PF00069 | 0.515 |
MOD_CDK_SPxK_1 | 408 | 414 | PF00069 | 0.340 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.713 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.321 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.266 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.335 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.299 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.694 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.595 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.586 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.663 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.652 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.562 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.313 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.391 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.295 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.339 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.271 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.494 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.444 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.266 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.321 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.524 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.657 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.624 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.608 |
MOD_GlcNHglycan | 644 | 649 | PF01048 | 0.578 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.350 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.210 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.686 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.310 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.343 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.366 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.333 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.411 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.727 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.549 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.570 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.639 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.657 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.655 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.646 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.622 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.486 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.496 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.321 |
MOD_N-GLC_1 | 515 | 520 | PF02516 | 0.435 |
MOD_N-GLC_1 | 621 | 626 | PF02516 | 0.757 |
MOD_N-GLC_2 | 652 | 654 | PF02516 | 0.553 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.256 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.287 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.301 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.285 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.585 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.588 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.554 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.597 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.562 |
MOD_NEK2_1 | 689 | 694 | PF00069 | 0.469 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.468 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.413 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.265 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.420 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.768 |
MOD_PIKK_1 | 621 | 627 | PF00454 | 0.707 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.576 |
MOD_PK_1 | 424 | 430 | PF00069 | 0.326 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.824 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.346 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.267 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.311 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.289 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.321 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.420 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.702 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.693 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.554 |
MOD_PKA_2 | 717 | 723 | PF00069 | 0.583 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.439 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.321 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.246 |
MOD_Plk_2-3 | 148 | 154 | PF00069 | 0.266 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.285 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.326 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.587 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.321 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.315 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.494 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.428 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.519 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.561 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.727 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.544 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.321 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.340 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.520 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.623 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.305 |
MOD_SUMO_rev_2 | 176 | 183 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 231 | 239 | PF00179 | 0.328 |
MOD_SUMO_rev_2 | 265 | 274 | PF00179 | 0.381 |
MOD_SUMO_rev_2 | 347 | 355 | PF00179 | 0.291 |
MOD_SUMO_rev_2 | 402 | 411 | PF00179 | 0.338 |
MOD_SUMO_rev_2 | 460 | 466 | PF00179 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 102 | 107 | PF01217 | 0.246 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.410 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 704 | 706 | PF00400 | 0.460 |
TRG_NES_CRM1_1 | 249 | 262 | PF08389 | 0.333 |
TRG_NLS_MonoCore_2 | 37 | 42 | PF00514 | 0.389 |
TRG_NLS_MonoCore_2 | 501 | 506 | PF00514 | 0.452 |
TRG_NLS_MonoExtC_3 | 36 | 41 | PF00514 | 0.359 |
TRG_NLS_MonoExtC_3 | 501 | 507 | PF00514 | 0.377 |
TRG_NLS_MonoExtN_4 | 37 | 42 | PF00514 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.220 |
TRG_Pf-PMV_PEXEL_1 | 421 | 426 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 450 | 454 | PF00026 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P647 | Leptomonas seymouri | 70% | 99% |
A0A0S4IJP8 | Bodo saltans | 50% | 97% |
A0A1X0NNY0 | Trypanosomatidae | 64% | 100% |
A0A3Q8IEL2 | Leishmania donovani | 30% | 100% |
A0A3S7WS99 | Leishmania donovani | 100% | 100% |
A0A3S7X9Y1 | Leishmania donovani | 32% | 100% |
A0A422NBP2 | Trypanosoma rangeli | 64% | 100% |
A4H720 | Leishmania braziliensis | 86% | 100% |
A4HND6 | Leishmania braziliensis | 31% | 100% |
A4I4V3 | Leishmania infantum | 30% | 100% |
A4IC09 | Leishmania infantum | 32% | 100% |
D0A6W1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AEA1 | Leishmania major | 30% | 100% |
E9AFU7 | Leishmania major | 32% | 100% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AP47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4QGE1 | Leishmania major | 95% | 100% |