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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030684 | preribosome | 3 | 11 |
GO:0030688 | preribosome, small subunit precursor | 4 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0030687 | preribosome, large subunit precursor | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AQP7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006364 | rRNA processing | 8 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016072 | rRNA metabolic process | 7 | 11 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.558 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.568 |
CLV_PCSK_FUR_1 | 629 | 633 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.812 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.746 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 477 | 479 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 639 | 641 | PF00082 | 0.619 |
CLV_PCSK_PC7_1 | 125 | 131 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.809 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.624 |
CLV_Separin_Metazoa | 406 | 410 | PF03568 | 0.486 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.613 |
DEG_SPOP_SBC_1 | 388 | 392 | PF00917 | 0.288 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.685 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 105 | 113 | PF00134 | 0.613 |
DOC_MAPK_gen_1 | 266 | 275 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 9 | 17 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.589 |
DOC_PP1_RVXF_1 | 244 | 250 | PF00149 | 0.355 |
DOC_PP2B_LxvP_1 | 237 | 240 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 443 | 446 | PF00568 | 0.382 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.249 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.638 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.616 |
DOC_USP7_UBL2_3 | 473 | 477 | PF12436 | 0.682 |
DOC_USP7_UBL2_3 | 593 | 597 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.636 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 528 | 538 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 539 | 547 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.501 |
LIG_APCC_ABBAyCdc20_2 | 648 | 654 | PF00400 | 0.610 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.486 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.425 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.563 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.571 |
LIG_GBD_Chelix_1 | 374 | 382 | PF00786 | 0.511 |
LIG_IBAR_NPY_1 | 102 | 104 | PF08397 | 0.627 |
LIG_LIR_Apic_2 | 441 | 446 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 197 | 207 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 401 | 412 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 414 | 425 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 545 | 550 | PF02991 | 0.573 |
LIG_MAD2 | 438 | 446 | PF02301 | 0.413 |
LIG_PCNA_TLS_4 | 266 | 273 | PF02747 | 0.447 |
LIG_PCNA_TLS_4 | 437 | 444 | PF02747 | 0.398 |
LIG_REV1ctd_RIR_1 | 510 | 520 | PF16727 | 0.454 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.747 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 106 | 109 | PF00017 | 0.596 |
LIG_SH2_NCK_1 | 153 | 157 | PF00017 | 0.669 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.585 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.622 |
LIG_SH3_1 | 95 | 101 | PF00018 | 0.637 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.689 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.651 |
LIG_SH3_4 | 222 | 229 | PF00018 | 0.335 |
LIG_SUMO_SIM_anti_2 | 201 | 206 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 32 | 37 | PF11976 | 0.564 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.568 |
LIG_TYR_ITIM | 248 | 253 | PF00017 | 0.447 |
LIG_Vh1_VBS_1 | 360 | 378 | PF01044 | 0.262 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.250 |
MOD_CDC14_SPxK_1 | 303 | 306 | PF00782 | 0.713 |
MOD_CDK_SPxK_1 | 300 | 306 | PF00069 | 0.714 |
MOD_CDK_SPxxK_3 | 300 | 307 | PF00069 | 0.771 |
MOD_CDK_SPxxK_3 | 314 | 321 | PF00069 | 0.735 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.753 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.549 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.571 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.799 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.614 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.482 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.710 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.580 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.508 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.570 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.714 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.738 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.529 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.473 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.436 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.512 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.558 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.508 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.635 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.461 |
MOD_PIKK_1 | 468 | 474 | PF00454 | 0.636 |
MOD_PKA_1 | 473 | 479 | PF00069 | 0.728 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.748 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.570 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.517 |
MOD_PKB_1 | 189 | 197 | PF00069 | 0.581 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.734 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.480 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.573 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.355 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.571 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.402 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.245 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.770 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.734 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.568 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.681 |
MOD_SUMO_for_1 | 305 | 308 | PF00179 | 0.755 |
MOD_SUMO_rev_2 | 560 | 566 | PF00179 | 0.649 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 556 | 558 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.616 |
TRG_NLS_Bipartite_1 | 620 | 635 | PF00514 | 0.584 |
TRG_NLS_MonoCore_2 | 638 | 643 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 629 | 635 | PF00514 | 0.593 |
TRG_NLS_MonoExtN_4 | 639 | 644 | PF00514 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 255 | 260 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6R2 | Leptomonas seymouri | 68% | 97% |
A0A0S4JIU4 | Bodo saltans | 36% | 100% |
A0A3S7WTZ9 | Leishmania donovani | 91% | 99% |
A0A422NDR1 | Trypanosoma rangeli | 39% | 100% |
A4H8L2 | Leishmania braziliensis | 84% | 100% |
A4HWY4 | Leishmania infantum | 91% | 99% |
C9ZW19 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4QET0 | Leishmania major | 91% | 100% |
V5BD23 | Trypanosoma cruzi | 37% | 100% |