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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005858 | axonemal dynein complex | 4 | 12 |
GO:0005875 | microtubule associated complex | 2 | 12 |
GO:0030286 | dynein complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQI2
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 12 |
GO:0070286 | axonemal dynein complex assembly | 6 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
GO:0003352 | regulation of cilium movement | 6 | 1 |
GO:0032886 | regulation of microtubule-based process | 4 | 1 |
GO:0048870 | cell motility | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0060285 | cilium-dependent cell motility | 4 | 1 |
GO:0060632 | regulation of microtubule-based movement | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.231 |
CLV_PCSK_FUR_1 | 221 | 225 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.640 |
CLV_PCSK_PC7_1 | 552 | 558 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.553 |
CLV_Separin_Metazoa | 218 | 222 | PF03568 | 0.276 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.310 |
DEG_APCC_KENBOX_2 | 299 | 303 | PF00400 | 0.456 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.483 |
DOC_CKS1_1 | 630 | 635 | PF01111 | 0.344 |
DOC_CYCLIN_yCln2_LP_2 | 400 | 406 | PF00134 | 0.375 |
DOC_MAPK_DCC_7 | 429 | 438 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 308 | 316 | PF00069 | 0.333 |
DOC_MAPK_HePTP_8 | 426 | 438 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 429 | 438 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 391 | 397 | PF00149 | 0.249 |
DOC_PP1_SILK_1 | 446 | 451 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.374 |
DOC_SPAK_OSR1_1 | 454 | 458 | PF12202 | 0.316 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.424 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.350 |
DOC_USP7_UBL2_3 | 361 | 365 | PF12436 | 0.435 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 180 | 187 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 287 | 291 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 486 | 496 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 635 | 644 | PF00244 | 0.489 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.515 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.540 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.540 |
LIG_eIF4E_1 | 631 | 637 | PF01652 | 0.486 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.433 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.609 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.407 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.416 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.483 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.389 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.406 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.492 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.563 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.569 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.364 |
LIG_LIR_Apic_2 | 629 | 634 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 625 | 631 | PF02991 | 0.488 |
LIG_NRBOX | 319 | 325 | PF00104 | 0.521 |
LIG_PCNA_yPIPBox_3 | 310 | 324 | PF02747 | 0.427 |
LIG_PCNA_yPIPBox_3 | 608 | 618 | PF02747 | 0.424 |
LIG_SH2_CRK | 631 | 635 | PF00017 | 0.504 |
LIG_SH2_PTP2 | 161 | 164 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 186 | 189 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 208 | 211 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 230 | 233 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 290 | 293 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 590 | 593 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.373 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.375 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 505 | 513 | PF11976 | 0.593 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.491 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.486 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.537 |
LIG_TRAF2_1 | 529 | 532 | PF00917 | 0.492 |
LIG_TYR_ITIM | 497 | 502 | PF00017 | 0.431 |
LIG_UBA3_1 | 444 | 450 | PF00899 | 0.416 |
LIG_WW_3 | 632 | 636 | PF00397 | 0.562 |
MOD_CDK_SPxK_1 | 629 | 635 | PF00069 | 0.345 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.596 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.579 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.462 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.429 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.582 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.429 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.444 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.529 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.372 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.530 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.480 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.431 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.420 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.351 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.591 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.495 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.431 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.349 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.563 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.516 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.500 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.598 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.372 |
MOD_N-GLC_1 | 487 | 492 | PF02516 | 0.533 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.520 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.507 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.508 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.589 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.399 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.353 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.425 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.421 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.652 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.435 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.572 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.556 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.497 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.416 |
MOD_PIKK_1 | 585 | 591 | PF00454 | 0.486 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.660 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.467 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.459 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.445 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.539 |
MOD_PKB_1 | 16 | 24 | PF00069 | 0.504 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.413 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.385 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.467 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.503 |
MOD_Plk_1 | 622 | 628 | PF00069 | 0.345 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.504 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.380 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.503 |
MOD_SUMO_for_1 | 259 | 262 | PF00179 | 0.309 |
MOD_SUMO_for_1 | 360 | 363 | PF00179 | 0.295 |
MOD_SUMO_rev_2 | 198 | 207 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 210 | 219 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 229 | 239 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 41 | 51 | PF00179 | 0.588 |
MOD_SUMO_rev_2 | 431 | 439 | PF00179 | 0.415 |
MOD_SUMO_rev_2 | 531 | 536 | PF00179 | 0.560 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_1 | 171 | 176 | PF01217 | 0.603 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.374 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_1 | 613 | 618 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_2 | 134 | 140 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.289 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.361 |
TRG_NLS_MonoExtN_4 | 308 | 314 | PF00514 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.316 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAH6 | Leptomonas seymouri | 66% | 100% |
A0A0S4J8E8 | Bodo saltans | 40% | 100% |
A0A1X0NL92 | Trypanosomatidae | 48% | 100% |
A0A3R7KG47 | Trypanosoma rangeli | 44% | 99% |
A0A3S7XCE4 | Leishmania donovani | 82% | 100% |
D0A3N0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AHZ1 | Leishmania infantum | 82% | 100% |
E9AU95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
F1QRC1 | Danio rerio | 26% | 97% |
P0DL09 | Chlamydomonas reinhardtii | 27% | 93% |
Q32KY1 | Bos taurus | 25% | 91% |
Q3USS3 | Mus musculus | 24% | 86% |
Q4Q096 | Leishmania major | 81% | 100% |
Q7T0Y4 | Xenopus laevis | 26% | 94% |
V5BD07 | Trypanosoma cruzi | 49% | 100% |