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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0070761 | pre-snoRNP complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AZJ1
Term | Name | Level | Count |
---|---|---|---|
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
GO:0000491 | small nucleolar ribonucleoprotein complex assembly | 7 | 1 |
GO:0000492 | box C/D snoRNP assembly | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006403 | RNA localization | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048254 | snoRNA localization | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 627 | 629 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 508 | 510 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 581 | 583 | PF00082 | 0.463 |
CLV_PCSK_PC7_1 | 199 | 205 | PF00082 | 0.474 |
CLV_PCSK_PC7_1 | 522 | 528 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 577 | 583 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.337 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.329 |
DOC_CKS1_1 | 405 | 410 | PF01111 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 191 | 197 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 121 | 129 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 122 | 131 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 142 | 150 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 392 | 400 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 453 | 460 | PF00149 | 0.330 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.394 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.386 |
DOC_PP4_FxxP_1 | 622 | 625 | PF00568 | 0.680 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.497 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.423 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 489 | 493 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 507 | 514 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 566 | 570 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 72 | 80 | PF00244 | 0.575 |
LIG_14-3-3_CterR_2 | 626 | 630 | PF00244 | 0.655 |
LIG_APCC_ABBA_1 | 129 | 134 | PF00400 | 0.440 |
LIG_EVH1_1 | 398 | 402 | PF00568 | 0.510 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.319 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.423 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.367 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.526 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.655 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.737 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.824 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.651 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.610 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.505 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.329 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.390 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.498 |
LIG_LIR_Gen_1 | 161 | 166 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 424 | 432 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 445 | 454 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 554 | 562 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 554 | 558 | PF02991 | 0.372 |
LIG_Pex14_1 | 184 | 188 | PF04695 | 0.496 |
LIG_Pex14_1 | 235 | 239 | PF04695 | 0.310 |
LIG_Pex14_2 | 416 | 420 | PF04695 | 0.448 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.312 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.367 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.552 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.437 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 114 | 118 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.461 |
LIG_SH2_PTP2 | 426 | 429 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 394 | 398 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.633 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.391 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.624 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.557 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.494 |
LIG_SUMO_SIM_anti_2 | 339 | 346 | PF11976 | 0.544 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.669 |
LIG_TRFH_1 | 442 | 446 | PF08558 | 0.425 |
MOD_CDC14_SPxK_1 | 592 | 595 | PF00782 | 0.503 |
MOD_CDK_SPK_2 | 404 | 409 | PF00069 | 0.417 |
MOD_CDK_SPxK_1 | 589 | 595 | PF00069 | 0.498 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.592 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.582 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.408 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.790 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.602 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.617 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.617 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.587 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.438 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.384 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.276 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.478 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.484 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.686 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.465 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.558 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.472 |
MOD_GlcNHglycan | 28 | 32 | PF01048 | 0.701 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.630 |
MOD_GlcNHglycan | 330 | 335 | PF01048 | 0.633 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.710 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.535 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.568 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.446 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.669 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.650 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.666 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.716 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.386 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.676 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.474 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.648 |
MOD_OFUCOSY | 119 | 124 | PF10250 | 0.357 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.619 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.350 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.633 |
MOD_PK_1 | 122 | 128 | PF00069 | 0.376 |
MOD_PKA_1 | 507 | 513 | PF00069 | 0.586 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.475 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.511 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.382 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.495 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.474 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.378 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.462 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.313 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.623 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.498 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.386 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.445 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.584 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.514 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.375 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.487 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.504 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.498 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.660 |
MOD_SUMO_rev_2 | 134 | 139 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 221 | 230 | PF00179 | 0.523 |
MOD_SUMO_rev_2 | 482 | 487 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_2 | 461 | 467 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 274 | 279 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.364 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 506 | 509 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 594 | 597 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 625 | 628 | PF00400 | 0.706 |
TRG_NES_CRM1_1 | 448 | 462 | PF08389 | 0.385 |
TRG_NLS_MonoExtC_3 | 579 | 584 | PF00514 | 0.454 |
TRG_NLS_MonoExtN_4 | 577 | 584 | PF00514 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 156 | 161 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 532 | 537 | PF00026 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0N9 | Leptomonas seymouri | 57% | 100% |
A0A3Q8IQB2 | Leishmania donovani | 89% | 100% |
A0A422N6T6 | Trypanosoma rangeli | 46% | 100% |
A4HG71 | Leishmania braziliensis | 77% | 100% |
A4I3B4 | Leishmania infantum | 89% | 100% |
D0A7T3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
Q4Q8P0 | Leishmania major | 88% | 100% |
V5BJ07 | Trypanosoma cruzi | 47% | 100% |