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:0005737 | cytoplasm | 2 | 1 |
GO:0005868 | cytoplasmic dynein complex | 4 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0030286 | dynein complex | 3 | 1 |
GO:0030990 | intraciliary transport particle | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A4HH18
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: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:0005515 | protein binding | 2 | 1 |
GO:0045503 | dynein light chain binding | 3 | 1 |
GO:0045504 | dynein heavy chain binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.476 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.433 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.454 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.544 |
DEG_APCC_DBOX_1 | 403 | 411 | PF00400 | 0.382 |
DEG_APCC_DBOX_1 | 448 | 456 | PF00400 | 0.425 |
DOC_CYCLIN_RxL_1 | 381 | 392 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 288 | 294 | PF00134 | 0.377 |
DOC_MAPK_gen_1 | 122 | 129 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 172 | 178 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.379 |
DOC_PP1_RVXF_1 | 466 | 472 | PF00149 | 0.206 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.376 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.243 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.322 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.307 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 198 | 208 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 438 | 445 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 508 | 512 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.586 |
LIG_Actin_WH2_2 | 492 | 510 | PF00022 | 0.426 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.558 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.421 |
LIG_BIR_III_4 | 482 | 486 | PF00653 | 0.397 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 202 | 206 | PF00533 | 0.311 |
LIG_Clathr_ClatBox_1 | 331 | 335 | PF01394 | 0.377 |
LIG_Clathr_ClatBox_1 | 407 | 411 | PF01394 | 0.493 |
LIG_CSL_BTD_1 | 281 | 284 | PF09270 | 0.261 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.526 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.589 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.312 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.464 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.344 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.491 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.488 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.431 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.416 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.521 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.597 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.460 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.367 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.518 |
LIG_HCF-1_HBM_1 | 265 | 268 | PF13415 | 0.289 |
LIG_LIR_Apic_2 | 344 | 348 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.418 |
LIG_PDZ_Class_1 | 529 | 534 | PF00595 | 0.491 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.402 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.480 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.519 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.414 |
LIG_SH2_SRC | 77 | 80 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 421 | 424 | PF00017 | 0.241 |
LIG_SH2_STAT3 | 445 | 448 | PF00017 | 0.217 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.438 |
LIG_SH3_2 | 259 | 264 | PF14604 | 0.315 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.492 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.527 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.285 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.453 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.310 |
LIG_SUMO_SIM_anti_2 | 125 | 132 | PF11976 | 0.498 |
LIG_SUMO_SIM_anti_2 | 247 | 254 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 276 | 283 | PF11976 | 0.204 |
LIG_SUMO_SIM_anti_2 | 327 | 333 | PF11976 | 0.326 |
LIG_SUMO_SIM_anti_2 | 431 | 437 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 212 | 218 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 276 | 283 | PF11976 | 0.204 |
LIG_SUMO_SIM_par_1 | 358 | 365 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 405 | 411 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 431 | 437 | PF11976 | 0.330 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.455 |
LIG_WRC_WIRS_1 | 89 | 94 | PF05994 | 0.467 |
LIG_WW_3 | 17 | 21 | PF00397 | 0.446 |
MOD_CDC14_SPxK_1 | 426 | 429 | PF00782 | 0.294 |
MOD_CDK_SPxK_1 | 423 | 429 | PF00069 | 0.295 |
MOD_CDK_SPxxK_3 | 132 | 139 | PF00069 | 0.382 |
MOD_CDK_SPxxK_3 | 280 | 287 | PF00069 | 0.399 |
MOD_CDK_SPxxK_3 | 377 | 384 | PF00069 | 0.390 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.252 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.400 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.411 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.470 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.346 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.404 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.313 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.491 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.556 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.653 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.610 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.355 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.382 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.462 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.356 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.441 |
MOD_GlcNHglycan | 165 | 169 | PF01048 | 0.472 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.231 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.294 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.525 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.267 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.290 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.449 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.229 |
MOD_GlcNHglycan | 411 | 415 | PF01048 | 0.340 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.454 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.360 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.482 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.348 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.422 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.353 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.325 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.374 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.304 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.407 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.415 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.328 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.253 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.454 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.487 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.600 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.481 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.467 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.485 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.379 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.266 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.503 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.491 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.530 |
MOD_NEK2_2 | 293 | 298 | PF00069 | 0.475 |
MOD_NEK2_2 | 525 | 530 | PF00069 | 0.353 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.349 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.503 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.527 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.457 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.634 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.377 |
MOD_PKA_1 | 122 | 128 | PF00069 | 0.466 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.588 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.450 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.447 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.341 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.325 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.487 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.588 |
MOD_PKB_1 | 21 | 29 | PF00069 | 0.447 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.457 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.443 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.555 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.465 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.511 |
MOD_Plk_2-3 | 88 | 94 | PF00069 | 0.298 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.269 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.496 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.415 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.307 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.433 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.425 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.635 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.239 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.385 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.358 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.314 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.261 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.407 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.304 |
TRG_DiLeu_BaEn_2 | 87 | 93 | PF01217 | 0.299 |
TRG_DiLeu_LyEn_5 | 403 | 408 | PF01217 | 0.467 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUS1 | Leptomonas seymouri | 64% | 100% |
A0A0S4INJ7 | Bodo saltans | 24% | 82% |
A0A0S4KLW0 | Bodo saltans | 42% | 96% |
A0A1X0NJ43 | Trypanosomatidae | 22% | 79% |
A0A1X0P0W1 | Trypanosomatidae | 48% | 100% |
A0A3S5IRX8 | Trypanosoma rangeli | 48% | 100% |
A0A3S7X1Z8 | Leishmania donovani | 81% | 100% |
A4I447 | Leishmania infantum | 80% | 100% |
C9ZKR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9ADL2 | Leishmania major | 79% | 100% |
E9AM69 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9PYY5 | Mus musculus | 24% | 66% |
P54703 | Dictyostelium discoideum | 21% | 82% |
Q16959 | Heliocidaris crassispina | 21% | 76% |
Q16960 | Heliocidaris crassispina | 23% | 89% |
Q32KS2 | Bos taurus | 21% | 76% |
Q39578 | Chlamydomonas reinhardtii | 24% | 78% |
Q4QR00 | Xenopus laevis | 24% | 91% |
Q4V8G4 | Rattus norvegicus | 22% | 67% |
Q5U4F6 | Mus musculus | 30% | 99% |
Q96EX3 | Homo sapiens | 31% | 100% |
Q9UI46 | Homo sapiens | 21% | 76% |
V5B145 | Trypanosoma cruzi | 22% | 89% |
V5BUI1 | Trypanosoma cruzi | 48% | 100% |