Flagella, intraflagellar transport C3 (PIFTC3) Uncharacterized
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) | yes | yes: 6 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 14 |
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 | 2 |
GO:0031514 | motile cilium | 5 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
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:0036064 | ciliary basal body | 3 | 1 |
GO:0097546 | ciliary base | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IEI7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 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:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0035720 | intraciliary anterograde transport | 4 | 1 |
GO:0035735 | intraciliary transport involved in cilium assembly | 4 | 1 |
GO:0042073 | intraciliary transport | 3 | 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:0099111 | microtubule-based transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0120170 | intraciliary transport particle B binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.436 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.658 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 240 | 250 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 447 | 457 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 504 | 511 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 186 | 195 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 243 | 252 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 378 | 387 | PF00069 | 0.407 |
DOC_MAPK_NFAT4_5 | 243 | 251 | PF00069 | 0.571 |
DOC_PP1_SILK_1 | 465 | 470 | PF00149 | 0.552 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.464 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.549 |
DOC_USP7_UBL2_3 | 557 | 561 | PF12436 | 0.445 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 168 | 178 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 254 | 258 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 477 | 483 | PF00244 | 0.547 |
LIG_APCC_ABBA_1 | 81 | 86 | PF00400 | 0.380 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 65 | 72 | PF00928 | 0.536 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.556 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.550 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.466 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.432 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.478 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.402 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.676 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.489 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.300 |
LIG_FXI_DFP_1 | 377 | 381 | PF00024 | 0.463 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 397 | 407 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.313 |
LIG_MLH1_MIPbox_1 | 371 | 375 | PF16413 | 0.395 |
LIG_NRP_CendR_1 | 566 | 568 | PF00754 | 0.681 |
LIG_Pex14_2 | 512 | 516 | PF04695 | 0.428 |
LIG_PTB_Apo_2 | 105 | 112 | PF02174 | 0.426 |
LIG_PTB_Apo_2 | 470 | 477 | PF02174 | 0.402 |
LIG_PTB_Phospho_1 | 470 | 476 | PF10480 | 0.393 |
LIG_REV1ctd_RIR_1 | 372 | 380 | PF16727 | 0.412 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.420 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.414 |
LIG_SH2_GRB2like | 106 | 109 | PF00017 | 0.570 |
LIG_SH2_GRB2like | 219 | 222 | PF00017 | 0.569 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.545 |
LIG_SH2_SRC | 402 | 405 | PF00017 | 0.383 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.547 |
LIG_SH2_SRC | 500 | 503 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 435 | 439 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.382 |
LIG_SH2_STAT3 | 333 | 336 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.441 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.586 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.536 |
LIG_SUMO_SIM_anti_2 | 208 | 213 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 523 | 530 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 420 | 427 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 86 | 92 | PF11976 | 0.458 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.669 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.521 |
LIG_TRAF2_1 | 517 | 520 | PF00917 | 0.457 |
LIG_TYR_ITIM | 202 | 207 | PF00017 | 0.534 |
LIG_UBA3_1 | 130 | 137 | PF00899 | 0.427 |
LIG_UBA3_1 | 384 | 391 | PF00899 | 0.419 |
LIG_UBA3_1 | 525 | 530 | PF00899 | 0.482 |
LIG_UBA3_1 | 552 | 561 | PF00899 | 0.430 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.556 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.450 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.410 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.494 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.472 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.477 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.654 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.454 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.298 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.599 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.474 |
MOD_Cter_Amidation | 502 | 505 | PF01082 | 0.416 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.450 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.558 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.674 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.528 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.545 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.323 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.454 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.461 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.457 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.568 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.476 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.404 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.400 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.494 |
MOD_N-GLC_2 | 473 | 475 | PF02516 | 0.394 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.673 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.559 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.521 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.431 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.396 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.629 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.465 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.402 |
MOD_NEK2_2 | 386 | 391 | PF00069 | 0.416 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.564 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.488 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.541 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.578 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.550 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.409 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.409 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.420 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.439 |
MOD_Plk_1 | 532 | 538 | PF00069 | 0.462 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.488 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.509 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.519 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.642 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.568 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.416 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.414 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.558 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.555 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.399 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.464 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.509 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.672 |
MOD_SUMO_for_1 | 242 | 245 | PF00179 | 0.537 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.444 |
MOD_SUMO_for_1 | 457 | 460 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 140 | 145 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 244 | 249 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 558 | 565 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_1 | 245 | 250 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_1 | 308 | 313 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 466 | 471 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.423 |
TRG_ER_diLys_1 | 564 | 568 | PF00400 | 0.586 |
TRG_NES_CRM1_1 | 279 | 291 | PF08389 | 0.539 |
TRG_NES_CRM1_1 | 460 | 474 | PF08389 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 469 | 474 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K7 | Leptomonas seymouri | 83% | 100% |
A0A0S4KM55 | Bodo saltans | 64% | 100% |
A0A1X0PAC6 | Trypanosomatidae | 68% | 100% |
A0A3R7NBU5 | Trypanosoma rangeli | 68% | 100% |
A0AVF1 | Homo sapiens | 49% | 100% |
A4HHT3 | Leishmania braziliensis | 93% | 100% |
A4I4Z3 | Leishmania infantum | 100% | 100% |
A4III8 | Xenopus tropicalis | 51% | 100% |
A8JA42 | Chlamydomonas reinhardtii | 48% | 100% |
C9ZKK5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9AED8 | Leishmania major | 98% | 100% |
E9ALE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
Q4R7Z9 | Macaca fascicularis | 50% | 100% |
Q57ZL2 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 68% | 100% |
Q5PR66 | Danio rerio | 52% | 100% |
Q5U2N8 | Rattus norvegicus | 50% | 100% |
Q8BS45 | Mus musculus | 50% | 100% |
Q95QT8 | Caenorhabditis elegans | 35% | 99% |
V5BXA0 | Trypanosoma cruzi | 69% | 100% |