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: 2 |
Pissara et al. | yes | yes: 10 |
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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005874 | microtubule | 6 | 4 |
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 | 4 |
GO:0099081 | supramolecular polymer | 3 | 4 |
GO:0099512 | supramolecular fiber | 4 | 4 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HQ31
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 15 |
GO:0007018 | microtubule-based movement | 3 | 15 |
GO:0009987 | cellular process | 1 | 15 |
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 | 15 |
GO:0003774 | cytoskeletal motor activity | 1 | 15 |
GO:0003777 | microtubule motor activity | 2 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005515 | protein binding | 2 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0008017 | microtubule binding | 5 | 15 |
GO:0008092 | cytoskeletal protein binding | 3 | 15 |
GO:0015631 | tubulin binding | 4 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140657 | ATP-dependent activity | 1 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 2 |
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_NRD_NRD_1 | 348 | 350 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 584 | 586 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 501 | 503 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.690 |
CLV_PCSK_PC7_1 | 497 | 503 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.373 |
CLV_Separin_Metazoa | 605 | 609 | PF03568 | 0.391 |
DEG_APCC_DBOX_1 | 335 | 343 | PF00400 | 0.294 |
DEG_APCC_KENBOX_2 | 492 | 496 | PF00400 | 0.425 |
DEG_Kelch_Keap1_1 | 290 | 295 | PF01344 | 0.321 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.440 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.540 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 263 | 271 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 97 | 105 | PF00069 | 0.214 |
DOC_MAPK_RevD_3 | 487 | 502 | PF00069 | 0.428 |
DOC_PP2B_LxvP_1 | 578 | 581 | PF13499 | 0.434 |
DOC_PP2B_PxIxI_1 | 100 | 106 | PF00149 | 0.214 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.495 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.607 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.750 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.400 |
DOC_USP7_UBL2_3 | 223 | 227 | PF12436 | 0.214 |
DOC_USP7_UBL2_3 | 441 | 445 | PF12436 | 0.518 |
DOC_USP7_UBL2_3 | 511 | 515 | PF12436 | 0.588 |
DOC_USP7_UBL2_3 | 617 | 621 | PF12436 | 0.669 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.623 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.383 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 244 | 251 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 552 | 559 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.469 |
LIG_APCC_ABBA_1 | 328 | 333 | PF00400 | 0.387 |
LIG_APCC_ABBAyCdc20_2 | 440 | 446 | PF00400 | 0.380 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.348 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.476 |
LIG_CaM_IQ_9 | 339 | 354 | PF13499 | 0.543 |
LIG_deltaCOP1_diTrp_1 | 67 | 72 | PF00928 | 0.451 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.302 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.307 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.438 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.609 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.371 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.447 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.383 |
LIG_KLC1_Yacidic_2 | 174 | 178 | PF13176 | 0.385 |
LIG_LIR_Apic_2 | 248 | 254 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 71 | 75 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 12 | 21 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 174 | 182 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 305 | 316 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.373 |
LIG_NRBOX | 269 | 275 | PF00104 | 0.369 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.457 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.393 |
LIG_SH2_NCK_1 | 110 | 114 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 572 | 576 | PF00017 | 0.559 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.349 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.693 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.214 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.349 |
LIG_SH3_1 | 15 | 21 | PF00018 | 0.517 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.517 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.386 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.524 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.340 |
LIG_SUMO_SIM_anti_2 | 174 | 181 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 385 | 391 | PF11976 | 0.623 |
LIG_SUMO_SIM_anti_2 | 398 | 403 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 44 | 50 | PF11976 | 0.454 |
LIG_TRAF2_1 | 567 | 570 | PF00917 | 0.586 |
LIG_UBA3_1 | 221 | 227 | PF00899 | 0.214 |
LIG_WRC_WIRS_1 | 69 | 74 | PF05994 | 0.449 |
MOD_CAAXbox | 622 | 625 | PF01239 | 0.468 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.364 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.447 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.522 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.428 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.430 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.421 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.556 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.574 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.476 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.469 |
MOD_DYRK1A_RPxSP_1 | 17 | 21 | PF00069 | 0.533 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.389 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.356 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.445 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.411 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.503 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.315 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.536 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.591 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.547 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.400 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.398 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.554 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.503 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.542 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.587 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.468 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.368 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.467 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.530 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.480 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.621 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.352 |
MOD_N-GLC_1 | 532 | 537 | PF02516 | 0.492 |
MOD_N-GLC_2 | 577 | 579 | PF02516 | 0.429 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.452 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.499 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.564 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.465 |
MOD_NEK2_2 | 192 | 197 | PF00069 | 0.214 |
MOD_NEK2_2 | 76 | 81 | PF00069 | 0.541 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.214 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.495 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.389 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.214 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.423 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.689 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.375 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.612 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.576 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.576 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.349 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.376 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.450 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.409 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.599 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.448 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.459 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.434 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.392 |
MOD_SUMO_for_1 | 402 | 405 | PF00179 | 0.524 |
MOD_SUMO_for_1 | 514 | 517 | PF00179 | 0.516 |
MOD_SUMO_for_1 | 593 | 596 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 371 | 376 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 474 | 480 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 505 | 513 | PF00179 | 0.659 |
MOD_SUMO_rev_2 | 542 | 548 | PF00179 | 0.557 |
TRG_DiLeu_BaEn_4 | 604 | 610 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 488 | 491 | PF00400 | 0.431 |
TRG_NLS_MonoExtN_4 | 347 | 353 | PF00514 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 501 | 505 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 586 | 590 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1K9 | Leptomonas seymouri | 66% | 100% |
A0A0S4JFN9 | Bodo saltans | 22% | 73% |
A0A0S4JPE8 | Bodo saltans | 32% | 69% |
A0A0S4JRN9 | Bodo saltans | 23% | 95% |
A0A1X0NNI2 | Trypanosomatidae | 23% | 68% |
A0A1X0P435 | Trypanosomatidae | 42% | 100% |
A0A3S7XBW9 | Leishmania donovani | 75% | 100% |
A0A422NMD1 | Trypanosoma rangeli | 41% | 100% |
A4HCT2 | Leishmania braziliensis | 23% | 87% |
A4IDT7 | Leishmania infantum | 75% | 100% |
D0A8T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9ATU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
P46873 | Caenorhabditis elegans | 23% | 89% |
Q4Q0P7 | Leishmania major | 74% | 100% |
V5B6Q5 | Trypanosoma cruzi | 43% | 100% |