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: E9AM69
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 | 521 | 525 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.608 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.555 |
DEG_APCC_DBOX_1 | 403 | 411 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.444 |
DOC_CYCLIN_RxL_1 | 381 | 392 | PF00134 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 288 | 294 | PF00134 | 0.438 |
DOC_MAPK_gen_1 | 122 | 129 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 172 | 178 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 341 | 349 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 438 | 444 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.418 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.450 |
DOC_USP7_MATH_2 | 348 | 354 | PF00917 | 0.593 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.700 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.357 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 341 | 346 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 510 | 514 | PF00244 | 0.601 |
LIG_Actin_WH2_2 | 174 | 189 | PF00022 | 0.455 |
LIG_Actin_WH2_2 | 494 | 512 | PF00022 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.629 |
LIG_BIR_III_4 | 484 | 488 | PF00653 | 0.445 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 202 | 206 | PF00533 | 0.424 |
LIG_BRCT_BRCA1_1 | 379 | 383 | PF00533 | 0.333 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.242 |
LIG_Clathr_ClatBox_1 | 331 | 335 | PF01394 | 0.442 |
LIG_Clathr_ClatBox_1 | 407 | 411 | PF01394 | 0.519 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.574 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.600 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.454 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.552 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.513 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.517 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.629 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.525 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.665 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.481 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.451 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.421 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.558 |
LIG_LIR_Apic_2 | 344 | 348 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.428 |
LIG_MLH1_MIPbox_1 | 379 | 383 | PF16413 | 0.333 |
LIG_PAM2_1 | 470 | 482 | PF00658 | 0.205 |
LIG_PDZ_Class_1 | 531 | 536 | PF00595 | 0.622 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.466 |
LIG_REV1ctd_RIR_1 | 380 | 388 | PF16727 | 0.421 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.468 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.448 |
LIG_SH2_SRC | 322 | 325 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.497 |
LIG_SH3_1 | 424 | 430 | PF00018 | 0.465 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.540 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.495 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.349 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.486 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 125 | 132 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 247 | 254 | PF11976 | 0.516 |
LIG_SUMO_SIM_anti_2 | 327 | 333 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 431 | 437 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 212 | 218 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 360 | 365 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 405 | 416 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 431 | 437 | PF11976 | 0.385 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.410 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.499 |
LIG_WRC_WIRS_1 | 89 | 94 | PF05994 | 0.524 |
MOD_CDC14_SPxK_1 | 426 | 429 | PF00782 | 0.354 |
MOD_CDK_SPxK_1 | 423 | 429 | PF00069 | 0.357 |
MOD_CDK_SPxxK_3 | 132 | 139 | PF00069 | 0.445 |
MOD_CDK_SPxxK_3 | 280 | 287 | PF00069 | 0.466 |
MOD_CDK_SPxxK_3 | 377 | 384 | PF00069 | 0.443 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.480 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.442 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.336 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.669 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.424 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.368 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.492 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.527 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.701 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.473 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.397 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.452 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.463 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.412 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.504 |
MOD_GlcNHglycan | 165 | 169 | PF01048 | 0.524 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.356 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.546 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.335 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.358 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.485 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.396 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.513 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.547 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.407 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.439 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.621 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.452 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.210 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.457 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.471 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.554 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.401 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.322 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.412 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.524 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.618 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.522 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.441 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.564 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.435 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.375 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.589 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.547 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.315 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.409 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.622 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.596 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.438 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.569 |
MOD_NEK2_2 | 293 | 298 | PF00069 | 0.503 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.408 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.621 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.652 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.510 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.474 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.569 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.282 |
MOD_PK_1 | 301 | 307 | PF00069 | 0.483 |
MOD_PKA_1 | 122 | 128 | PF00069 | 0.514 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.640 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.542 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.540 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.365 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.355 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.505 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.396 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.616 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.497 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.452 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.564 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.270 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.431 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.473 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.562 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.485 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.348 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.491 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.650 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.282 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.433 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.349 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.459 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.354 |
TRG_DiLeu_LyEn_5 | 403 | 408 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P997 | Leptomonas seymouri | 23% | 89% |
A0A0N1HUS1 | Leptomonas seymouri | 67% | 100% |
A0A0S4INJ7 | Bodo saltans | 23% | 83% |
A0A0S4KLW0 | Bodo saltans | 41% | 96% |
A0A1X0NUK4 | Trypanosomatidae | 25% | 89% |
A0A1X0P0W1 | Trypanosomatidae | 47% | 100% |
A0A3S5IRX8 | Trypanosoma rangeli | 47% | 100% |
A0A3S7X1Z8 | Leishmania donovani | 95% | 100% |
A0A3S7X5B2 | Leishmania donovani | 24% | 89% |
A0A422P1D5 | Trypanosoma rangeli | 24% | 89% |
A2AC93 | Mus musculus | 24% | 86% |
A4HH18 | Leishmania braziliensis | 81% | 100% |
A4HK88 | Leishmania braziliensis | 24% | 100% |
A4I447 | Leishmania infantum | 95% | 100% |
A4I7S3 | Leishmania infantum | 24% | 89% |
C9ZKR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9ADL2 | Leishmania major | 94% | 100% |
E9PYY5 | Mus musculus | 24% | 66% |
P54703 | Dictyostelium discoideum | 21% | 82% |
Q16959 | Heliocidaris crassispina | 23% | 76% |
Q16960 | Heliocidaris crassispina | 25% | 90% |
Q24246 | Drosophila melanogaster | 26% | 81% |
Q32KS2 | Bos taurus | 22% | 76% |
Q39578 | Chlamydomonas reinhardtii | 24% | 78% |
Q4Q5H6 | Leishmania major | 23% | 100% |
Q4QR00 | Xenopus laevis | 23% | 91% |
Q4V8G4 | Rattus norvegicus | 23% | 67% |
Q5U4F6 | Mus musculus | 29% | 100% |
Q5XIL8 | Rattus norvegicus | 22% | 76% |
Q8C0M8 | Mus musculus | 22% | 76% |
Q96EX3 | Homo sapiens | 30% | 100% |
Q9UI46 | Homo sapiens | 20% | 77% |
V5B145 | Trypanosoma cruzi | 25% | 89% |
V5BUI1 | Trypanosoma cruzi | 48% | 100% |