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: 0 |
Pissara et al. | no | yes: 12 |
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. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 12 |
GO:0031514 | motile cilium | 5 | 12 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 12 |
GO:0005814 | centriole | 5 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0030990 | intraciliary transport particle | 2 | 1 |
GO:0030992 | intraciliary transport particle B | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0035869 | ciliary transition zone | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S5H752
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 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:0035735 | intraciliary transport involved in cilium assembly | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 631 | 635 | PF00656 | 0.337 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.475 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.481 |
CLV_Separin_Metazoa | 381 | 385 | PF03568 | 0.446 |
DEG_APCC_DBOX_1 | 462 | 470 | PF00400 | 0.491 |
DEG_APCC_DBOX_1 | 503 | 511 | PF00400 | 0.385 |
DEG_APCC_DBOX_1 | 663 | 671 | PF00400 | 0.488 |
DEG_SCF_FBW7_2 | 94 | 100 | PF00400 | 0.454 |
DOC_ANK_TNKS_1 | 106 | 113 | PF00023 | 0.423 |
DOC_CKS1_1 | 426 | 431 | PF01111 | 0.522 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 285 | 291 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 421 | 424 | PF00134 | 0.474 |
DOC_MAPK_DCC_7 | 411 | 421 | PF00069 | 0.578 |
DOC_MAPK_DCC_7 | 443 | 452 | PF00069 | 0.503 |
DOC_MAPK_FxFP_2 | 258 | 261 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 304 | 313 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 63 | 73 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 443 | 452 | PF00069 | 0.491 |
DOC_MAPK_RevD_3 | 505 | 519 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 38 | 45 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 421 | 424 | PF13499 | 0.474 |
DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.298 |
DOC_PP4_FxxP_1 | 426 | 429 | PF00568 | 0.493 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.393 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.424 |
DOC_USP7_UBL2_3 | 411 | 415 | PF12436 | 0.430 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 82 | 92 | PF00244 | 0.528 |
LIG_Actin_WH2_2 | 636 | 654 | PF00022 | 0.377 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.596 |
LIG_BIR_III_2 | 567 | 571 | PF00653 | 0.504 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.584 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.367 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.387 |
LIG_BRCT_BRCA1_1 | 599 | 603 | PF00533 | 0.427 |
LIG_CaM_NSCaTE_8 | 626 | 633 | PF13499 | 0.491 |
LIG_Clathr_ClatBox_1 | 389 | 393 | PF01394 | 0.505 |
LIG_Clathr_ClatBox_1 | 452 | 456 | PF01394 | 0.482 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.442 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.719 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.676 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.731 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.384 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.327 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.494 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.430 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.435 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.354 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.316 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.369 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.351 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.465 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.547 |
LIG_GBD_Chelix_1 | 332 | 340 | PF00786 | 0.453 |
LIG_LIR_Apic_2 | 14 | 19 | PF02991 | 0.647 |
LIG_LIR_Apic_2 | 255 | 261 | PF02991 | 0.326 |
LIG_LIR_Apic_2 | 425 | 429 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 334 | 344 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 385 | 392 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 407 | 416 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 516 | 520 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 625 | 629 | PF02991 | 0.380 |
LIG_PDZ_Class_3 | 668 | 673 | PF00595 | 0.418 |
LIG_Pex14_2 | 319 | 323 | PF04695 | 0.475 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.429 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.388 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.423 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.486 |
LIG_SH2_GRB2like | 130 | 133 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 640 | 643 | PF00017 | 0.482 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.396 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.395 |
LIG_SH2_SRC | 339 | 342 | PF00017 | 0.456 |
LIG_SH2_SRC | 580 | 583 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 481 | 484 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.512 |
LIG_SH3_1 | 48 | 54 | PF00018 | 0.359 |
LIG_SH3_2 | 429 | 434 | PF14604 | 0.501 |
LIG_SH3_2 | 51 | 56 | PF14604 | 0.371 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.586 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.369 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.486 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.486 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.359 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.479 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 417 | 423 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 99 | 107 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 309 | 315 | PF11976 | 0.312 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.658 |
LIG_TRAF2_1 | 526 | 529 | PF00917 | 0.713 |
LIG_TRAF2_1 | 669 | 672 | PF00917 | 0.502 |
LIG_TYR_ITIM | 478 | 483 | PF00017 | 0.524 |
LIG_TYR_ITIM | 515 | 520 | PF00017 | 0.461 |
LIG_TYR_ITIM | 638 | 643 | PF00017 | 0.479 |
LIG_UBA3_1 | 336 | 345 | PF00899 | 0.330 |
LIG_UBA3_1 | 389 | 396 | PF00899 | 0.480 |
LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.450 |
MOD_CDC14_SPxK_1 | 6 | 9 | PF00782 | 0.585 |
MOD_CDK_SPK_2 | 494 | 499 | PF00069 | 0.483 |
MOD_CDK_SPxK_1 | 3 | 9 | PF00069 | 0.589 |
MOD_CDK_SPxxK_3 | 494 | 501 | PF00069 | 0.477 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.507 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.689 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.492 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.397 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.346 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.442 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.533 |
MOD_Cter_Amidation | 177 | 180 | PF01082 | 0.421 |
MOD_Cter_Amidation | 302 | 305 | PF01082 | 0.476 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.344 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.646 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.706 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.664 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.652 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.344 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.322 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.629 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.438 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.564 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.469 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.479 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.612 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.309 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.565 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.446 |
MOD_N-GLC_2 | 45 | 47 | PF02516 | 0.375 |
MOD_N-GLC_2 | 471 | 473 | PF02516 | 0.399 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.588 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.544 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.435 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.428 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.442 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.631 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.577 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.404 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.395 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.466 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.559 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.344 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.334 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.632 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.549 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.457 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.540 |
MOD_Plk_1 | 598 | 604 | PF00069 | 0.527 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.409 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.442 |
MOD_Plk_2-3 | 76 | 82 | PF00069 | 0.409 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.392 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.491 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.672 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.386 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.349 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.473 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.564 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.651 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.523 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.479 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.446 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 414 | 417 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 338 | 344 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 607 | 617 | PF00179 | 0.569 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 417 | 422 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_4 | 327 | 333 | PF01217 | 0.339 |
TRG_DiLeu_BaLyEn_6 | 271 | 276 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.602 |
TRG_NES_CRM1_1 | 380 | 393 | PF08389 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 504 | 508 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDM4 | Leptomonas seymouri | 80% | 99% |
A0A0S4KG78 | Bodo saltans | 55% | 100% |
A0A1X0P7F0 | Trypanosomatidae | 66% | 100% |
A0A3R7NUY6 | Trypanosoma rangeli | 64% | 100% |
A4H9Z0 | Leishmania braziliensis | 86% | 99% |
A4HY54 | Leishmania infantum | 100% | 100% |
D0A0G1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9ARY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QDI9 | Leishmania major | 95% | 100% |
V5DTK4 | Trypanosoma cruzi | 65% | 100% |