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:0005930 | axoneme | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0044297 | cell body | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9B2J7
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0022607 | cellular component assembly | 4 | 11 |
GO:0036158 | outer dynein arm assembly | 7 | 11 |
GO:0036159 | inner dynein arm assembly | 7 | 11 |
GO:0043933 | protein-containing complex organization | 4 | 11 |
GO:0065003 | protein-containing complex assembly | 5 | 11 |
GO:0070286 | axonemal dynein complex assembly | 6 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0044458 | motile cilium assembly | 7 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0048870 | cell motility | 2 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0060285 | cilium-dependent cell motility | 4 | 1 |
GO:0070925 | organelle assembly | 5 | 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:0005488 | binding | 1 | 11 |
GO:0044877 | protein-containing complex binding | 2 | 11 |
GO:0070840 | dynein complex binding | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 515 | 519 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 523 | 527 | PF00656 | 0.605 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.365 |
CLV_PCSK_FUR_1 | 336 | 340 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.793 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.518 |
CLV_Separin_Metazoa | 480 | 484 | PF03568 | 0.677 |
DOC_CDC14_PxL_1 | 249 | 257 | PF14671 | 0.432 |
DOC_CKS1_1 | 467 | 472 | PF01111 | 0.592 |
DOC_CYCLIN_RxL_1 | 375 | 385 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 467 | 473 | PF00134 | 0.670 |
DOC_MAPK_gen_1 | 242 | 252 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 586 | 596 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 245 | 252 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 67 | 75 | PF00069 | 0.388 |
DOC_MAPK_NFAT4_5 | 245 | 253 | PF00069 | 0.425 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.353 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.441 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.631 |
DOC_PP4_FxxP_1 | 450 | 453 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.266 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 261 | 271 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 528 | 536 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 539 | 543 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 568 | 574 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 588 | 596 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.430 |
LIG_APCC_ABBA_1 | 41 | 46 | PF00400 | 0.498 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.482 |
LIG_Clathr_ClatBox_1 | 481 | 485 | PF01394 | 0.655 |
LIG_deltaCOP1_diTrp_1 | 364 | 373 | PF00928 | 0.572 |
LIG_deltaCOP1_diTrp_1 | 576 | 585 | PF00928 | 0.575 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.734 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.616 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.505 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.398 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.370 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.516 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.356 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.456 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.252 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.462 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.687 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.472 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.627 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.534 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.579 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.612 |
LIG_LIR_Apic_2 | 448 | 453 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 146 | 155 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 576 | 587 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 576 | 582 | PF02991 | 0.582 |
LIG_LRP6_Inhibitor_1 | 75 | 81 | PF00058 | 0.430 |
LIG_NRBOX | 477 | 483 | PF00104 | 0.663 |
LIG_PDZ_Class_2 | 591 | 596 | PF00595 | 0.532 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.345 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.673 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.739 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.627 |
MOD_CDC14_SPxK_1 | 452 | 455 | PF00782 | 0.487 |
MOD_CDK_SPxK_1 | 449 | 455 | PF00069 | 0.491 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.433 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.462 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.645 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.704 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.729 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.541 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.503 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.293 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.439 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.491 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.619 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.561 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.593 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.792 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.435 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.603 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.582 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.703 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.602 |
MOD_GlcNHglycan | 59 | 63 | PF01048 | 0.494 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.306 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.339 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.531 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.645 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.721 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.625 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.690 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.596 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.472 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.336 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.494 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.488 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.350 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.330 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.227 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.671 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.594 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.409 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.333 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.194 |
MOD_NEK2_2 | 102 | 107 | PF00069 | 0.430 |
MOD_NEK2_2 | 432 | 437 | PF00069 | 0.468 |
MOD_NEK2_2 | 69 | 74 | PF00069 | 0.266 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.560 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.526 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.509 |
MOD_PIKK_1 | 588 | 594 | PF00454 | 0.714 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.512 |
MOD_PKA_1 | 568 | 574 | PF00069 | 0.630 |
MOD_PKA_1 | 588 | 594 | PF00069 | 0.623 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.551 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.497 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.507 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.679 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.652 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.623 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.650 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.364 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.599 |
MOD_Plk_1 | 575 | 581 | PF00069 | 0.392 |
MOD_Plk_2-3 | 285 | 291 | PF00069 | 0.497 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.369 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.432 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.531 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.612 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.302 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.659 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 285 | 295 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 407 | 414 | PF00179 | 0.694 |
MOD_SUMO_rev_2 | 42 | 50 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_1 | 133 | 138 | PF01217 | 0.320 |
TRG_DiLeu_BaEn_4 | 133 | 139 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.735 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P804 | Leptomonas seymouri | 59% | 99% |
A0A0S4KIJ3 | Bodo saltans | 37% | 100% |
A0A3Q8IJ31 | Leishmania donovani | 88% | 100% |
A0A3R7KFT3 | Trypanosoma rangeli | 48% | 100% |
A4HK54 | Leishmania braziliensis | 77% | 100% |
A4I7P0 | Leishmania infantum | 88% | 100% |
D0A9U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
Q4Q5K9 | Leishmania major | 87% | 100% |
V5D6Q2 | Trypanosoma cruzi | 48% | 100% |