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: 0 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005875 | microtubule associated complex | 2 | 11 |
GO:0030286 | dynein complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:0005868 | cytoplasmic dynein complex | 4 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0031514 | motile cilium | 5 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7X4D8
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0007018 | microtubule-based movement | 3 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0010970 | transport along microtubule | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0035721 | intraciliary retrograde transport | 4 | 1 |
GO:0042073 | intraciliary transport | 3 | 1 |
GO:0044782 | cilium 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:0060271 | cilium assembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0099111 | microtubule-based transport | 4 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 11 |
GO:0003777 | microtubule motor activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0008569 | minus-end-directed microtubule motor activity | 3 | 11 |
GO:0045505 | dynein intermediate chain binding | 3 | 11 |
GO:0051959 | dynein light intermediate chain binding | 3 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 462 | 466 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.551 |
CLV_PCSK_FUR_1 | 295 | 299 | PF00082 | 0.551 |
CLV_PCSK_FUR_1 | 310 | 314 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 544 | 546 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.553 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.482 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 441 | 449 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 505 | 511 | PF00134 | 0.511 |
DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.478 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.585 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 437 | 441 | PF12436 | 0.505 |
DOC_USP7_UBL2_3 | 533 | 537 | PF12436 | 0.678 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.645 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 240 | 247 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 41 | 45 | PF00244 | 0.425 |
LIG_Actin_WH2_2 | 406 | 424 | PF00022 | 0.578 |
LIG_APCC_ABBAyCdc20_2 | 428 | 434 | PF00400 | 0.458 |
LIG_Clathr_ClatBox_1 | 47 | 51 | PF01394 | 0.472 |
LIG_CSL_BTD_1 | 348 | 351 | PF09270 | 0.571 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.721 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.705 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.440 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.531 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.449 |
LIG_Integrin_isoDGR_2 | 614 | 616 | PF01839 | 0.492 |
LIG_LIR_Apic_2 | 173 | 177 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.453 |
LIG_PTB_Apo_2 | 235 | 242 | PF02174 | 0.449 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 379 | 383 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 403 | 407 | PF00017 | 0.485 |
LIG_SH2_PTP2 | 174 | 177 | PF00017 | 0.531 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.471 |
LIG_SH2_SRC | 403 | 406 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.634 |
LIG_SH3_1 | 366 | 372 | PF00018 | 0.644 |
LIG_SH3_2 | 13 | 18 | PF14604 | 0.683 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.492 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.644 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.599 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.694 |
LIG_SH3_4 | 537 | 544 | PF00018 | 0.624 |
LIG_SH3_CIN85_PxpxPR_1 | 336 | 341 | PF14604 | 0.595 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 408 | 414 | PF11976 | 0.666 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.565 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.482 |
LIG_TRFH_1 | 235 | 239 | PF08558 | 0.451 |
LIG_UBA3_1 | 525 | 533 | PF00899 | 0.496 |
LIG_UBA3_1 | 584 | 590 | PF00899 | 0.526 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.691 |
MOD_CDC14_SPxK_1 | 9 | 12 | PF00782 | 0.713 |
MOD_CDK_SPK_2 | 336 | 341 | PF00069 | 0.717 |
MOD_CDK_SPK_2 | 347 | 352 | PF00069 | 0.762 |
MOD_CDK_SPK_2 | 361 | 366 | PF00069 | 0.550 |
MOD_CDK_SPK_2 | 6 | 11 | PF00069 | 0.699 |
MOD_CDK_SPxK_1 | 6 | 12 | PF00069 | 0.725 |
MOD_CDK_SPxxK_3 | 361 | 368 | PF00069 | 0.674 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.700 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.417 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.679 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.495 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.735 |
MOD_Cter_Amidation | 542 | 545 | PF01082 | 0.626 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.750 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.582 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.634 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.565 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.557 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.691 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.789 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.586 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.555 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.521 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.471 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.617 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.570 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.477 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.480 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.541 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.436 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.512 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.476 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.559 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.653 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.576 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.542 |
MOD_PK_1 | 33 | 39 | PF00069 | 0.488 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.719 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.503 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.651 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.415 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.472 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.536 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.562 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.616 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.641 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.673 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.441 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.575 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.436 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.648 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.687 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.808 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.644 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.527 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.645 |
MOD_SUMO_for_1 | 304 | 307 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 155 | 163 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 277 | 287 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 389 | 394 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 434 | 442 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 459 | 469 | PF00179 | 0.620 |
MOD_SUMO_rev_2 | 481 | 490 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 530 | 538 | PF00179 | 0.596 |
TRG_DiLeu_BaEn_1 | 521 | 526 | PF01217 | 0.507 |
TRG_DiLeu_BaEn_2 | 599 | 605 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_4 | 119 | 125 | PF01217 | 0.586 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.666 |
TRG_NES_CRM1_1 | 179 | 194 | PF08389 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 105 | 109 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 229 | 234 | PF00026 | 0.221 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 443 | 447 | PF00026 | 0.651 |
TRG_Pf-PMV_PEXEL_1 | 482 | 486 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 520 | 524 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 593 | 598 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILZ8 | Leptomonas seymouri | 25% | 67% |
A0A0N1PDQ0 | Leptomonas seymouri | 56% | 100% |
A0A1X0NQ11 | Trypanosomatidae | 36% | 74% |
A0A422NZ91 | Trypanosoma rangeli | 35% | 77% |
A4HJA9 | Leishmania braziliensis | 72% | 99% |
A4I6Q2 | Leishmania infantum | 100% | 100% |
E9B1S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q6D7 | Leishmania major | 92% | 100% |
V5DGE3 | Trypanosoma cruzi | 35% | 78% |