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: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 20 |
GO:0042995 | cell projection | 2 | 20 |
GO:0043226 | organelle | 2 | 20 |
GO:0043227 | membrane-bounded organelle | 3 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 20 |
GO:0005634 | nucleus | 5 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0005643 | nuclear pore | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AZ72
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0015931 | nucleobase-containing compound transport | 5 | 3 |
GO:0050657 | nucleic acid transport | 6 | 3 |
GO:0050658 | RNA transport | 4 | 3 |
GO:0051028 | mRNA transport | 5 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0051236 | establishment of RNA localization | 3 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 3 |
GO:0006405 | RNA export from nucleus | 5 | 2 |
GO:0006406 | mRNA export from nucleus | 6 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051168 | nuclear export | 6 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.534 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.438 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 441 | 443 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.411 |
DEG_SCF_FBW7_1 | 309 | 315 | PF00400 | 0.546 |
DOC_CDC14_PxL_1 | 275 | 283 | PF14671 | 0.420 |
DOC_CKS1_1 | 17 | 22 | PF01111 | 0.436 |
DOC_CKS1_1 | 309 | 314 | PF01111 | 0.548 |
DOC_CKS1_1 | 496 | 501 | PF01111 | 0.535 |
DOC_CYCLIN_RxL_1 | 256 | 263 | PF00134 | 0.316 |
DOC_MAPK_gen_1 | 257 | 264 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 531 | 539 | PF00069 | 0.372 |
DOC_PP1_RVXF_1 | 198 | 204 | PF00149 | 0.553 |
DOC_PP1_RVXF_1 | 68 | 74 | PF00149 | 0.372 |
DOC_PP2B_LxvP_1 | 223 | 226 | PF13499 | 0.574 |
DOC_PP4_FxxP_1 | 230 | 233 | PF00568 | 0.637 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.466 |
DOC_USP7_UBL2_3 | 200 | 204 | PF12436 | 0.551 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 335 | 345 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 358 | 362 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 46 | 53 | PF00244 | 0.714 |
LIG_APCC_ABBA_1 | 69 | 74 | PF00400 | 0.502 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.380 |
LIG_CaM_NSCaTE_8 | 209 | 216 | PF13499 | 0.343 |
LIG_deltaCOP1_diTrp_1 | 224 | 231 | PF00928 | 0.680 |
LIG_EH1_1 | 458 | 466 | PF00400 | 0.381 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.365 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.461 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.533 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.691 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.462 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.320 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.437 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.497 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.551 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.493 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.532 |
LIG_LIR_Gen_1 | 297 | 308 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 606 | 614 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 606 | 610 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.422 |
LIG_PCNA_PIPBox_1 | 65 | 74 | PF02747 | 0.392 |
LIG_PCNA_yPIPBox_3 | 252 | 265 | PF02747 | 0.551 |
LIG_PCNA_yPIPBox_3 | 372 | 380 | PF02747 | 0.442 |
LIG_Pex14_1 | 227 | 231 | PF04695 | 0.673 |
LIG_PTB_Apo_2 | 388 | 395 | PF02174 | 0.638 |
LIG_REV1ctd_RIR_1 | 21 | 30 | PF16727 | 0.536 |
LIG_REV1ctd_RIR_1 | 70 | 79 | PF16727 | 0.524 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.490 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.624 |
LIG_SH2_CRK | 530 | 534 | PF00017 | 0.209 |
LIG_SH2_SRC | 36 | 39 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 510 | 514 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 565 | 569 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.486 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.435 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.467 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.494 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.413 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.483 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.477 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.724 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.570 |
LIG_SUMO_SIM_anti_2 | 385 | 390 | PF11976 | 0.576 |
LIG_SUMO_SIM_anti_2 | 595 | 602 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 404 | 410 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 445 | 454 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 558 | 566 | PF11976 | 0.479 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.464 |
LIG_UBA3_1 | 346 | 350 | PF00899 | 0.645 |
LIG_UBA3_1 | 68 | 75 | PF00899 | 0.406 |
LIG_WRC_WIRS_1 | 261 | 266 | PF05994 | 0.233 |
LIG_WRC_WIRS_1 | 540 | 545 | PF05994 | 0.386 |
LIG_WRC_WIRS_1 | 93 | 98 | PF05994 | 0.473 |
MOD_CDK_SPxK_1 | 16 | 22 | PF00069 | 0.442 |
MOD_CDK_SPxK_1 | 308 | 314 | PF00069 | 0.491 |
MOD_CDK_SPxxK_3 | 318 | 325 | PF00069 | 0.556 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.469 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.520 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.460 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.557 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.485 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.532 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.486 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.543 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.484 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.286 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.676 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.451 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.556 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.670 |
MOD_GlcNHglycan | 606 | 610 | PF01048 | 0.497 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.415 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.372 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.353 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.436 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.655 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.339 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.518 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.444 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.428 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.411 |
MOD_LATS_1 | 165 | 171 | PF00433 | 0.341 |
MOD_LATS_1 | 38 | 44 | PF00433 | 0.638 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.519 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.660 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.412 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.561 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.418 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.398 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.584 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.422 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.400 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.556 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.352 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.438 |
MOD_NEK2_2 | 576 | 581 | PF00069 | 0.480 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.503 |
MOD_OFUCOSY | 114 | 120 | PF10250 | 0.465 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.575 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.414 |
MOD_PK_1 | 167 | 173 | PF00069 | 0.346 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.543 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.502 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.516 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.514 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.681 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.413 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.352 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.398 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.408 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.404 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.426 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.676 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.492 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.655 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.393 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.509 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.420 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.344 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.420 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.526 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.456 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.505 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.604 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.525 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.640 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.521 |
MOD_SUMO_for_1 | 363 | 366 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 135 | 142 | PF00179 | 0.523 |
MOD_SUMO_rev_2 | 195 | 201 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 385 | 394 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 515 | 523 | PF00179 | 0.488 |
TRG_DiLeu_BaEn_1 | 595 | 600 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.623 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.477 |
TRG_NLS_MonoExtC_3 | 5 | 11 | PF00514 | 0.557 |
TRG_NLS_MonoExtN_4 | 3 | 10 | PF00514 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E9 | Leptomonas seymouri | 70% | 98% |
A0A0N0P8S6 | Leptomonas seymouri | 25% | 100% |
A0A0S4IW66 | Bodo saltans | 30% | 100% |
A0A1X0P4A3 | Trypanosomatidae | 28% | 100% |
A0A1X0P4L1 | Trypanosomatidae | 44% | 100% |
A0A3R7NID6 | Trypanosoma rangeli | 44% | 100% |
A0A3S7X0T0 | Leishmania donovani | 25% | 100% |
A0A3S7X0T8 | Leishmania donovani | 95% | 100% |
A4HFU4 | Leishmania braziliensis | 85% | 100% |
A4I2W0 | Leishmania infantum | 25% | 100% |
A4I2W1 | Leishmania infantum | 95% | 100% |
D0A641 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A644 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ADE7 | Leishmania major | 24% | 100% |
E9ADE8 | Leishmania major | 94% | 100% |
E9AZ71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
V5B0W6 | Trypanosoma cruzi | 45% | 100% |
V5BQG4 | Trypanosoma cruzi | 27% | 100% |