Flagella, intraflagellar transport component
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | 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: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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HY54
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 | 632 | 636 | PF00656 | 0.407 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.551 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 665 | 669 | PF00082 | 0.551 |
CLV_Separin_Metazoa | 382 | 386 | PF03568 | 0.525 |
DEG_APCC_DBOX_1 | 463 | 471 | PF00400 | 0.553 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.459 |
DEG_APCC_DBOX_1 | 664 | 672 | PF00400 | 0.560 |
DEG_SCF_FBW7_2 | 94 | 100 | PF00400 | 0.612 |
DOC_ANK_TNKS_1 | 106 | 113 | PF00023 | 0.584 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.606 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 286 | 292 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 422 | 425 | PF00134 | 0.562 |
DOC_MAPK_DCC_7 | 412 | 422 | PF00069 | 0.646 |
DOC_MAPK_DCC_7 | 444 | 453 | PF00069 | 0.578 |
DOC_MAPK_FxFP_2 | 259 | 262 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 305 | 314 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 63 | 73 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 444 | 453 | PF00069 | 0.566 |
DOC_MAPK_RevD_3 | 506 | 520 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 38 | 45 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.562 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.388 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.474 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.512 |
DOC_USP7_UBL2_3 | 412 | 416 | PF12436 | 0.505 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 567 | 572 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 82 | 92 | PF00244 | 0.574 |
LIG_Actin_WH2_2 | 637 | 655 | PF00022 | 0.463 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.683 |
LIG_BIR_III_2 | 568 | 572 | PF00653 | 0.543 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.723 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.446 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.547 |
LIG_BRCT_BRCA1_1 | 600 | 604 | PF00533 | 0.516 |
LIG_CaM_NSCaTE_8 | 627 | 634 | PF13499 | 0.559 |
LIG_Clathr_ClatBox_1 | 390 | 394 | PF01394 | 0.582 |
LIG_Clathr_ClatBox_1 | 453 | 457 | PF01394 | 0.563 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.500 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.738 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.763 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.791 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.456 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.392 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.559 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.522 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.501 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.443 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.457 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.439 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.519 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.611 |
LIG_GBD_Chelix_1 | 333 | 341 | PF00786 | 0.520 |
LIG_LIR_Apic_2 | 14 | 19 | PF02991 | 0.810 |
LIG_LIR_Apic_2 | 256 | 262 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 426 | 430 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 335 | 345 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 386 | 393 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 408 | 417 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 509 | 515 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 517 | 521 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 626 | 630 | PF02991 | 0.464 |
LIG_PDZ_Class_3 | 669 | 674 | PF00595 | 0.506 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.539 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.505 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.448 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.515 |
LIG_SH2_CRK | 518 | 522 | PF00017 | 0.570 |
LIG_SH2_GRB2like | 130 | 133 | PF00017 | 0.457 |
LIG_SH2_PTP2 | 641 | 644 | PF00017 | 0.537 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.485 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.487 |
LIG_SH2_SRC | 340 | 343 | PF00017 | 0.521 |
LIG_SH2_SRC | 581 | 584 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 482 | 485 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 669 | 672 | PF00017 | 0.553 |
LIG_SH3_1 | 48 | 54 | PF00018 | 0.471 |
LIG_SH3_2 | 430 | 435 | PF14604 | 0.586 |
LIG_SH3_2 | 51 | 56 | PF14604 | 0.485 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.718 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.459 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.571 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.561 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.471 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.567 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.533 |
LIG_SUMO_SIM_anti_2 | 418 | 424 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 99 | 107 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.402 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.679 |
LIG_TRAF2_1 | 527 | 530 | PF00917 | 0.795 |
LIG_TRAF2_1 | 670 | 673 | PF00917 | 0.580 |
LIG_TYR_ITIM | 479 | 484 | PF00017 | 0.583 |
LIG_TYR_ITIM | 516 | 521 | PF00017 | 0.547 |
LIG_TYR_ITIM | 639 | 644 | PF00017 | 0.544 |
LIG_UBA3_1 | 337 | 346 | PF00899 | 0.420 |
LIG_UBA3_1 | 390 | 397 | PF00899 | 0.561 |
LIG_WRC_WIRS_1 | 393 | 398 | PF05994 | 0.535 |
MOD_CDC14_SPxK_1 | 6 | 9 | PF00782 | 0.716 |
MOD_CDK_SPK_2 | 495 | 500 | PF00069 | 0.535 |
MOD_CDK_SPxK_1 | 3 | 9 | PF00069 | 0.718 |
MOD_CDK_SPxxK_3 | 495 | 502 | PF00069 | 0.528 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.736 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.767 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.655 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.487 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.435 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.525 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.595 |
MOD_Cter_Amidation | 177 | 180 | PF01082 | 0.558 |
MOD_Cter_Amidation | 303 | 306 | PF01082 | 0.550 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.475 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.731 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.781 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.696 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.660 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.410 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.411 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.699 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.547 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.492 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.675 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.537 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.563 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.621 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.391 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.659 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.517 |
MOD_N-GLC_2 | 45 | 47 | PF02516 | 0.465 |
MOD_N-GLC_2 | 472 | 474 | PF02516 | 0.486 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.683 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.459 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.504 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.506 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.532 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.696 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.631 |
MOD_PIKK_1 | 465 | 471 | PF00454 | 0.490 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.490 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.540 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.590 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.430 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.421 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.689 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.576 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.505 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.606 |
MOD_Plk_1 | 599 | 605 | PF00069 | 0.600 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.495 |
MOD_Plk_2-3 | 365 | 371 | PF00069 | 0.525 |
MOD_Plk_2-3 | 76 | 82 | PF00069 | 0.495 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.421 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.503 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.700 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.447 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.424 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.561 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.696 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.731 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.607 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.527 |
MOD_ProDKin_1 | 567 | 573 | PF00069 | 0.497 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.578 |
MOD_SUMO_for_1 | 415 | 418 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 339 | 345 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 608 | 618 | PF00179 | 0.629 |
TRG_DiLeu_BaEn_1 | 253 | 258 | PF01217 | 0.574 |
TRG_DiLeu_BaEn_1 | 418 | 423 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_4 | 328 | 334 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 641 | 644 | PF00928 | 0.537 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.722 |
TRG_NES_CRM1_1 | 381 | 394 | PF08389 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 505 | 509 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDM4 | Leptomonas seymouri | 80% | 99% |
A0A0S4KG78 | Bodo saltans | 55% | 100% |
A0A1X0P7F0 | Trypanosomatidae | 65% | 100% |
A0A3R7NUY6 | Trypanosoma rangeli | 64% | 100% |
A0A3S5H752 | Leishmania donovani | 100% | 100% |
A4H9Z0 | Leishmania braziliensis | 87% | 99% |
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% |