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. | yes | 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. | no | 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:0005814 | centriole | 5 | 2 |
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0005929 | cilium | 4 | 12 |
GO:0030990 | intraciliary transport particle | 2 | 2 |
GO:0030992 | intraciliary transport particle B | 2 | 2 |
GO:0031514 | motile cilium | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0035869 | ciliary transition zone | 2 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 12 |
Related structures:
AlphaFold database: Q4QDI9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007018 | microtubule-based movement | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010970 | transport along microtubule | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0030031 | cell projection assembly | 5 | 2 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 2 |
GO:0031503 | protein-containing complex localization | 2 | 2 |
GO:0035735 | intraciliary transport involved in cilium assembly | 4 | 2 |
GO:0042073 | intraciliary transport | 3 | 2 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0060271 | cilium assembly | 6 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0099111 | microtubule-based transport | 4 | 2 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 2 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.550 |
CLV_Separin_Metazoa | 380 | 384 | PF03568 | 0.530 |
DEG_APCC_DBOX_1 | 461 | 469 | PF00400 | 0.548 |
DEG_APCC_DBOX_1 | 502 | 510 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 662 | 670 | PF00400 | 0.558 |
DEG_SCF_FBW7_2 | 567 | 572 | PF00400 | 0.408 |
DEG_SCF_FBW7_2 | 92 | 98 | PF00400 | 0.608 |
DOC_ANK_TNKS_1 | 104 | 111 | PF00023 | 0.579 |
DOC_CKS1_1 | 425 | 430 | PF01111 | 0.609 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.599 |
DOC_CYCLIN_yCln2_LP_2 | 284 | 290 | PF00134 | 0.417 |
DOC_CYCLIN_yCln2_LP_2 | 420 | 423 | PF00134 | 0.563 |
DOC_MAPK_DCC_7 | 410 | 420 | PF00069 | 0.643 |
DOC_MAPK_DCC_7 | 442 | 451 | PF00069 | 0.586 |
DOC_MAPK_FxFP_2 | 257 | 260 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 303 | 312 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 442 | 451 | PF00069 | 0.574 |
DOC_MAPK_RevD_3 | 504 | 518 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 37 | 43 | PF00149 | 0.473 |
DOC_PP2B_LxvP_1 | 420 | 423 | PF13499 | 0.563 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.384 |
DOC_PP4_FxxP_1 | 425 | 428 | PF00568 | 0.577 |
DOC_PP4_FxxP_1 | 89 | 92 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.674 |
DOC_USP7_UBL2_3 | 173 | 177 | PF12436 | 0.496 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.503 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 80 | 90 | PF00244 | 0.576 |
LIG_Actin_WH2_2 | 635 | 653 | PF00022 | 0.462 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.700 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.547 |
LIG_BRCT_BRCA1_1 | 598 | 602 | PF00533 | 0.517 |
LIG_CaM_NSCaTE_8 | 625 | 632 | PF13499 | 0.561 |
LIG_Clathr_ClatBox_1 | 388 | 392 | PF01394 | 0.586 |
LIG_Clathr_ClatBox_1 | 393 | 397 | PF01394 | 0.594 |
LIG_Clathr_ClatBox_1 | 451 | 455 | PF01394 | 0.560 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.520 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.790 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.759 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.474 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.415 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.549 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.564 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.514 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.438 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.513 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.606 |
LIG_GBD_Chelix_1 | 331 | 339 | PF00786 | 0.520 |
LIG_LIR_Apic_2 | 14 | 19 | PF02991 | 0.803 |
LIG_LIR_Apic_2 | 254 | 260 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 424 | 428 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 356 | 365 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 515 | 519 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 624 | 628 | PF02991 | 0.459 |
LIG_PDZ_Class_3 | 667 | 672 | PF00595 | 0.503 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.540 |
LIG_Pex14_2 | 385 | 389 | PF04695 | 0.508 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.446 |
LIG_SH2_CRK | 408 | 412 | PF00017 | 0.511 |
LIG_SH2_CRK | 516 | 520 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 128 | 131 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 639 | 642 | PF00017 | 0.536 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.479 |
LIG_SH2_SRC | 154 | 157 | PF00017 | 0.485 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.518 |
LIG_SH2_SRC | 579 | 582 | PF00017 | 0.547 |
LIG_SH2_STAT3 | 480 | 483 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.546 |
LIG_SH3_1 | 46 | 52 | PF00018 | 0.476 |
LIG_SH3_2 | 428 | 433 | PF14604 | 0.578 |
LIG_SH3_2 | 49 | 54 | PF14604 | 0.488 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.722 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.456 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.559 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.562 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.476 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 416 | 422 | PF11976 | 0.548 |
LIG_SUMO_SIM_anti_2 | 97 | 105 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 113 | 120 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 308 | 314 | PF11976 | 0.398 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.735 |
LIG_TRAF2_1 | 525 | 528 | PF00917 | 0.775 |
LIG_TRAF2_1 | 668 | 671 | PF00917 | 0.576 |
LIG_TYR_ITIM | 477 | 482 | PF00017 | 0.587 |
LIG_TYR_ITIM | 514 | 519 | PF00017 | 0.545 |
LIG_TYR_ITIM | 637 | 642 | PF00017 | 0.524 |
LIG_UBA3_1 | 335 | 344 | PF00899 | 0.420 |
LIG_UBA3_1 | 388 | 395 | PF00899 | 0.569 |
MOD_CDC14_SPxK_1 | 6 | 9 | PF00782 | 0.717 |
MOD_CDK_SPK_2 | 493 | 498 | PF00069 | 0.574 |
MOD_CDK_SPxK_1 | 3 | 9 | PF00069 | 0.722 |
MOD_CDK_SPxxK_3 | 493 | 500 | PF00069 | 0.567 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.702 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.645 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.485 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.431 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.524 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.590 |
MOD_Cter_Amidation | 175 | 178 | PF01082 | 0.553 |
MOD_Cter_Amidation | 301 | 304 | PF01082 | 0.557 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.551 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.755 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.695 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.692 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.419 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.404 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.697 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.587 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.575 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.517 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.669 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.523 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.562 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.651 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.648 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.516 |
MOD_N-GLC_2 | 43 | 45 | PF02516 | 0.465 |
MOD_N-GLC_2 | 470 | 472 | PF02516 | 0.486 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.672 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.591 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.506 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.509 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.539 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.703 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.634 |
MOD_PIKK_1 | 463 | 469 | PF00454 | 0.469 |
MOD_PIKK_1 | 523 | 529 | PF00454 | 0.757 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.483 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.529 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.536 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.596 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.676 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.617 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.524 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.617 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.603 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.497 |
MOD_Plk_2-3 | 363 | 369 | PF00069 | 0.524 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.501 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.503 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.715 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.471 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.446 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.560 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.675 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.718 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.611 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.570 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.496 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.574 |
MOD_SUMO_for_1 | 413 | 416 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 337 | 343 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 606 | 616 | PF00179 | 0.634 |
TRG_DiLeu_BaEn_1 | 251 | 256 | PF01217 | 0.591 |
TRG_DiLeu_BaEn_1 | 416 | 421 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_4 | 326 | 332 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 270 | 275 | PF01217 | 0.524 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 516 | 519 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 462 | 465 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.787 |
TRG_NES_CRM1_1 | 379 | 392 | PF08389 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 503 | 507 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 61 | 65 | PF00026 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDM4 | Leptomonas seymouri | 79% | 99% |
A0A0S4KG78 | Bodo saltans | 54% | 100% |
A0A1X0P7F0 | Trypanosomatidae | 66% | 100% |
A0A3R7NUY6 | Trypanosoma rangeli | 65% | 100% |
A0A3S5H752 | Leishmania donovani | 95% | 100% |
A4H9Z0 | Leishmania braziliensis | 89% | 100% |
A4HY54 | Leishmania infantum | 95% | 100% |
D0A0G1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9ARY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5DTK4 | Trypanosoma cruzi | 65% | 100% |