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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QBR8
Term | Name | Level | Count |
---|---|---|---|
GO:0001731 | formation of translation preinitiation complex | 7 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 12 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 12 |
GO:0065003 | protein-containing complex assembly | 5 | 12 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.471 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.399 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.281 |
DEG_APCC_DBOX_1 | 234 | 242 | PF00400 | 0.581 |
DEG_APCC_KENBOX_2 | 245 | 249 | PF00400 | 0.544 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.325 |
DOC_CYCLIN_RxL_1 | 131 | 140 | PF00134 | 0.329 |
DOC_CYCLIN_RxL_1 | 424 | 434 | PF00134 | 0.515 |
DOC_MAPK_DCC_7 | 497 | 505 | PF00069 | 0.489 |
DOC_MAPK_DCC_7 | 564 | 573 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 153 | 160 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 20 | 29 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 326 | 336 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 497 | 505 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 622 | 632 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 187 | 196 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 497 | 505 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 516 | 524 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 564 | 573 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 625 | 634 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 330 | 337 | PF00149 | 0.561 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.376 |
DOC_PP2B_LxvP_1 | 298 | 301 | PF13499 | 0.409 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.421 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.515 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.559 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.458 |
DOC_USP7_UBL2_3 | 560 | 564 | PF12436 | 0.509 |
DOC_USP7_UBL2_3 | 625 | 629 | PF12436 | 0.469 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.585 |
LIG_14-3-3_CanoR_1 | 216 | 226 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 473 | 477 | PF00244 | 0.438 |
LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.384 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 591 | 595 | PF00533 | 0.547 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 202 | 212 | PF00928 | 0.379 |
LIG_eIF4E_1 | 471 | 477 | PF01652 | 0.510 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.478 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.682 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.501 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.520 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.570 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.568 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.530 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.474 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.731 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.421 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.425 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.525 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.495 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.542 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 412 | 418 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 202 | 213 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 270 | 276 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 36 | 42 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.436 |
LIG_LIR_LC3C_4 | 39 | 42 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.273 |
LIG_MYND_1 | 295 | 299 | PF01753 | 0.464 |
LIG_NRBOX | 105 | 111 | PF00104 | 0.495 |
LIG_NRP_CendR_1 | 663 | 665 | PF00754 | 0.565 |
LIG_OCRL_FandH_1 | 102 | 114 | PF00620 | 0.490 |
LIG_Pex14_1 | 604 | 608 | PF04695 | 0.448 |
LIG_Pex14_2 | 208 | 212 | PF04695 | 0.531 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.513 |
LIG_REV1ctd_RIR_1 | 99 | 109 | PF16727 | 0.455 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 271 | 275 | PF00017 | 0.531 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 271 | 275 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.372 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.474 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.466 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.434 |
LIG_SH3_3 | 611 | 617 | PF00018 | 0.491 |
LIG_SH3_4 | 625 | 632 | PF00018 | 0.528 |
LIG_SH3_5 | 267 | 271 | PF00018 | 0.601 |
LIG_SUMO_SIM_anti_2 | 162 | 168 | PF11976 | 0.417 |
LIG_SUMO_SIM_anti_2 | 25 | 31 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 156 | 162 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 342 | 350 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 427 | 434 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 488 | 494 | PF11976 | 0.529 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.561 |
LIG_UBA3_1 | 145 | 154 | PF00899 | 0.410 |
LIG_UBA3_1 | 531 | 536 | PF00899 | 0.500 |
LIG_WRC_WIRS_1 | 590 | 595 | PF05994 | 0.540 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.560 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.484 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.344 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.547 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.583 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.536 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.345 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.430 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.440 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.492 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.535 |
MOD_Cter_Amidation | 42 | 45 | PF01082 | 0.280 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.352 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.362 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.770 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.566 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.547 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.506 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.593 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.254 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.356 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.489 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.435 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.529 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.450 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.651 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.547 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.535 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.518 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.553 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.423 |
MOD_N-GLC_1 | 652 | 657 | PF02516 | 0.431 |
MOD_N-GLC_2 | 283 | 285 | PF02516 | 0.389 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.404 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.348 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.435 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.526 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.431 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.487 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.413 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.537 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.512 |
MOD_PIKK_1 | 654 | 660 | PF00454 | 0.473 |
MOD_PK_1 | 499 | 505 | PF00069 | 0.572 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.454 |
MOD_PKA_1 | 44 | 50 | PF00069 | 0.501 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.508 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.560 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.482 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.413 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.455 |
MOD_Plk_2-3 | 342 | 348 | PF00069 | 0.413 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.476 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.543 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.439 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.404 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.418 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.591 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.261 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.409 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.540 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.460 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.303 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.498 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.474 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.702 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.522 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.575 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.581 |
MOD_SUMO_rev_2 | 13 | 22 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 256 | 266 | PF00179 | 0.756 |
TRG_DiLeu_BaEn_1 | 116 | 121 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_3 | 81 | 87 | PF01217 | 0.345 |
TRG_DiLeu_BaLyEn_6 | 220 | 225 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.399 |
TRG_NES_CRM1_1 | 525 | 540 | PF08389 | 0.290 |
TRG_NLS_Bipartite_1 | 3 | 24 | PF00514 | 0.522 |
TRG_NLS_MonoExtC_3 | 152 | 157 | PF00514 | 0.504 |
TRG_NLS_MonoExtC_3 | 19 | 25 | PF00514 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 216 | 221 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 419 | 423 | PF00026 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I577 | Leptomonas seymouri | 57% | 95% |
A0A0S4INV2 | Bodo saltans | 25% | 75% |
A0A1X0NTA4 | Trypanosomatidae | 32% | 100% |
A0A3S5H7A8 | Leishmania donovani | 88% | 100% |
A0A422N4G3 | Trypanosoma rangeli | 33% | 100% |
A4HCD6 | Leishmania braziliensis | 76% | 100% |
A4HZV3 | Leishmania infantum | 88% | 100% |
C9ZSH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AVR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
V5BLJ1 | Trypanosoma cruzi | 34% | 92% |