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) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005874 | microtubule | 6 | 2 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0015630 | microtubule cytoskeleton | 6 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
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 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0099081 | supramolecular polymer | 3 | 2 |
GO:0099512 | supramolecular fiber | 4 | 2 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4IDT7
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 14 |
GO:0007018 | microtubule-based movement | 3 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0000902 | cell morphogenesis | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0009653 | anatomical structure morphogenesis | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 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:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003774 | cytoskeletal motor activity | 1 | 14 |
GO:0003777 | microtubule motor activity | 2 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0005515 | protein binding | 2 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0008017 | microtubule binding | 5 | 14 |
GO:0008092 | cytoskeletal protein binding | 3 | 14 |
GO:0015631 | tubulin binding | 4 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.271 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.481 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.531 |
CLV_PCSK_PC7_1 | 230 | 236 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.340 |
DOC_CKS1_1 | 199 | 204 | PF01111 | 0.406 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 263 | 271 | PF00069 | 0.367 |
DOC_MAPK_RevD_3 | 219 | 235 | PF00069 | 0.358 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.623 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.614 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 17 | 26 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 244 | 251 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 511 | 519 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 552 | 558 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.397 |
LIG_APCC_ABBA_1 | 328 | 333 | PF00400 | 0.356 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.351 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.434 |
LIG_CaM_IQ_9 | 222 | 237 | PF13499 | 0.382 |
LIG_CaM_IQ_9 | 339 | 354 | PF13499 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 67 | 72 | PF00928 | 0.529 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.461 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.270 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.390 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.568 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.323 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.407 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.347 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.500 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.684 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.465 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.314 |
LIG_KLC1_Yacidic_2 | 174 | 178 | PF13176 | 0.347 |
LIG_LIR_Apic_2 | 248 | 254 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 71 | 75 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 12 | 21 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 305 | 316 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 456 | 464 | PF02991 | 0.648 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.293 |
LIG_NRBOX | 269 | 275 | PF00104 | 0.334 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.384 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.425 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.293 |
LIG_SH2_NCK_1 | 110 | 114 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 572 | 576 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.323 |
LIG_SH2_SRC | 572 | 575 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.632 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.403 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.349 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.477 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.501 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.302 |
LIG_SUMO_SIM_anti_2 | 174 | 182 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 385 | 391 | PF11976 | 0.538 |
LIG_SUMO_SIM_anti_2 | 398 | 403 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 44 | 50 | PF11976 | 0.354 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.512 |
LIG_TRAF2_1 | 75 | 78 | PF00917 | 0.594 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.296 |
LIG_WRC_WIRS_1 | 69 | 74 | PF05994 | 0.367 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.309 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.336 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.356 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.401 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.393 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.401 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.412 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.553 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.381 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.383 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.525 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.508 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.495 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.640 |
MOD_CK2_1 | 599 | 605 | PF00069 | 0.604 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.450 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.303 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.348 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.449 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.359 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.479 |
MOD_GlcNHglycan | 29 | 33 | PF01048 | 0.581 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.423 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.410 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.655 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.356 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.373 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.513 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.495 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.439 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.385 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.327 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.490 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.548 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.518 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.599 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.387 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.455 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.653 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.627 |
MOD_PIKK_1 | 615 | 621 | PF00454 | 0.578 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.301 |
MOD_PK_1 | 512 | 518 | PF00069 | 0.453 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.391 |
MOD_PKA_1 | 615 | 621 | PF00069 | 0.615 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.399 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.398 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.307 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.509 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.610 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.620 |
MOD_PKB_1 | 15 | 23 | PF00069 | 0.317 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.296 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.540 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.533 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.549 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.271 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.287 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.436 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.531 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.447 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.420 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.420 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.313 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 402 | 405 | PF00179 | 0.478 |
MOD_SUMO_for_1 | 593 | 596 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 22 | 26 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 371 | 376 | PF00179 | 0.462 |
MOD_SUMO_rev_2 | 379 | 383 | PF00179 | 0.358 |
MOD_SUMO_rev_2 | 474 | 480 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 505 | 513 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 533 | 541 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 611 | 618 | PF00179 | 0.516 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 606 | 608 | PF00400 | 0.542 |
TRG_NES_CRM1_1 | 385 | 400 | PF08389 | 0.350 |
TRG_NES_CRM1_1 | 453 | 465 | PF08389 | 0.554 |
TRG_NLS_MonoExtN_4 | 347 | 353 | PF00514 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 35 | 39 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 529 | 534 | PF00026 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 607 | 611 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1K9 | Leptomonas seymouri | 69% | 100% |
A0A0S4IR67 | Bodo saltans | 23% | 80% |
A0A0S4J0Q2 | Bodo saltans | 22% | 75% |
A0A0S4JFN9 | Bodo saltans | 23% | 73% |
A0A0S4JPE8 | Bodo saltans | 33% | 69% |
A0A0S4JRN9 | Bodo saltans | 23% | 95% |
A0A1X0NWZ8 | Trypanosomatidae | 23% | 84% |
A0A1X0P435 | Trypanosomatidae | 43% | 100% |
A0A3R7KHX7 | Trypanosoma rangeli | 21% | 85% |
A0A3S7XBW9 | Leishmania donovani | 100% | 100% |
A0A422NMD1 | Trypanosoma rangeli | 45% | 100% |
A4HQ31 | Leishmania braziliensis | 75% | 100% |
D0A8T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ATU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P46873 | Caenorhabditis elegans | 22% | 89% |
Q1MTQ1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
Q4Q0P7 | Leishmania major | 94% | 100% |
Q4QEL8 | Leishmania major | 23% | 77% |
V5B6Q5 | Trypanosoma cruzi | 44% | 100% |
V5D733 | Trypanosoma cruzi | 23% | 83% |