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:0001534 | radial spoke | 2 | 12 |
GO:0005929 | cilium | 4 | 12 |
GO:0031514 | motile cilium | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 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:0005930 | axoneme | 2 | 1 |
GO:0097730 | non-motile cilium | 5 | 1 |
Related structures:
AlphaFold database: E9AP67
Term | Name | Level | Count |
---|---|---|---|
GO:0003341 | cilium movement | 4 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007018 | microtubule-based movement | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0030030 | cell projection organization | 4 | 11 |
GO:0030031 | cell projection assembly | 5 | 11 |
GO:0044782 | cilium organization | 5 | 11 |
GO:0060271 | cilium assembly | 6 | 11 |
GO:0060294 | cilium movement involved in cell motility | 5 | 12 |
GO:0070925 | organelle assembly | 5 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 11 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 11 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0001578 | microtubule bundle formation | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0035082 | axoneme assembly | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.117 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.351 |
CLV_PCSK_FUR_1 | 191 | 195 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.309 |
DEG_SCF_SKP2-CKS1_1 | 464 | 471 | PF00560 | 0.534 |
DOC_CKS1_1 | 421 | 426 | PF01111 | 0.358 |
DOC_MAPK_gen_1 | 211 | 221 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 331 | 340 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 525 | 532 | PF00069 | 0.460 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.534 |
DOC_PP4_FxxP_1 | 100 | 103 | PF00568 | 0.489 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.553 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.523 |
DOC_USP7_UBL2_3 | 211 | 215 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 375 | 379 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 292 | 301 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 525 | 532 | PF00244 | 0.543 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.573 |
LIG_BIR_III_4 | 403 | 407 | PF00653 | 0.553 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.443 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.498 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.514 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.473 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.473 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.467 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.448 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.489 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.553 |
LIG_FHA_2 | 557 | 563 | PF00498 | 0.496 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.539 |
LIG_Integrin_isoDGR_2 | 370 | 372 | PF01839 | 0.260 |
LIG_KLC1_Yacidic_2 | 200 | 205 | PF13176 | 0.534 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 132 | 138 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 242 | 253 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 31 | 40 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 420 | 425 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.467 |
LIG_NRBOX | 38 | 44 | PF00104 | 0.553 |
LIG_Pex14_1 | 527 | 531 | PF04695 | 0.460 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.489 |
LIG_REV1ctd_RIR_1 | 174 | 183 | PF16727 | 0.489 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.460 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.460 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 117 | 121 | PF00017 | 0.460 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.553 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.505 |
LIG_SH2_SRC | 429 | 432 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.534 |
LIG_SH2_STAT3 | 21 | 24 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.445 |
LIG_SH3_2 | 469 | 474 | PF14604 | 0.534 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.500 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.551 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.509 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.317 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.534 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.476 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.452 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.482 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.406 |
LIG_SH3_4 | 211 | 218 | PF00018 | 0.509 |
LIG_SH3_5 | 341 | 345 | PF00018 | 0.498 |
LIG_SUMO_SIM_par_1 | 336 | 342 | PF11976 | 0.562 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.460 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.460 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.460 |
LIG_TRAF2_1 | 413 | 416 | PF00917 | 0.498 |
LIG_TRAF2_1 | 454 | 457 | PF00917 | 0.502 |
LIG_TRAF2_1 | 86 | 89 | PF00917 | 0.534 |
LIG_WRC_WIRS_1 | 61 | 66 | PF05994 | 0.534 |
LIG_WW_3 | 211 | 215 | PF00397 | 0.526 |
MOD_CDK_SPxK_1 | 465 | 471 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 237 | 244 | PF00069 | 0.553 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.509 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.534 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.381 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.448 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.583 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.534 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.628 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.345 |
MOD_Cter_Amidation | 523 | 526 | PF01082 | 0.260 |
MOD_GlcNHglycan | 269 | 273 | PF01048 | 0.300 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.304 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.554 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.322 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.446 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.453 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.508 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.451 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.514 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.504 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.260 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.615 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.448 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.465 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.498 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.497 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.498 |
MOD_NEK2_2 | 489 | 494 | PF00069 | 0.473 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.553 |
MOD_PKA_1 | 525 | 531 | PF00069 | 0.553 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.448 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.553 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.515 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.448 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.553 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.448 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.515 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.523 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.553 |
MOD_Plk_2-3 | 580 | 586 | PF00069 | 0.628 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.523 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.498 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.448 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.418 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.462 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.501 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.394 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.555 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.357 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.534 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.446 |
MOD_SUMO_rev_2 | 168 | 177 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 89 | 99 | PF00179 | 0.498 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_2 | 59 | 65 | PF01217 | 0.534 |
TRG_DiLeu_BaEn_4 | 153 | 159 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 525 | 527 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 572 | 574 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.553 |
TRG_NES_CRM1_1 | 34 | 46 | PF08389 | 0.553 |
TRG_NLS_MonoExtN_4 | 211 | 218 | PF00514 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF4 | Leptomonas seymouri | 74% | 100% |
A0A0S4JGY1 | Bodo saltans | 50% | 100% |
A0A1X0NN98 | Trypanosomatidae | 58% | 100% |
A0A3S7WSD6 | Leishmania donovani | 94% | 99% |
A0A422NNZ6 | Trypanosoma rangeli | 57% | 100% |
A4H732 | Leishmania braziliensis | 88% | 99% |
A4HVG6 | Leishmania infantum | 95% | 100% |
D0A6U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
Q01656 | Chlamydomonas reinhardtii | 28% | 100% |
Q4QGB1 | Leishmania major | 93% | 99% |
Q9H0K4 | Homo sapiens | 28% | 83% |
V5BDZ5 | Trypanosoma cruzi | 58% | 92% |