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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
GO:0005682 | U5 snRNP | 5 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 1 |
GO:0071020 | post-spliceosomal complex | 4 | 1 |
GO:0071021 | U2-type post-spliceosomal complex | 5 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 1 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
Related structures:
AlphaFold database: E9AVS3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006396 | RNA processing | 6 | 6 |
GO:0006397 | mRNA processing | 7 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0008380 | RNA splicing | 7 | 6 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0016071 | mRNA metabolic process | 6 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:0000350 | generation of catalytic spliceosome for second transesterification step | 7 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.777 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.346 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.330 |
CLV_Separin_Metazoa | 329 | 333 | PF03568 | 0.346 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.546 |
DEG_ODPH_VHL_1 | 368 | 381 | PF01847 | 0.626 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.557 |
DOC_CKS1_1 | 162 | 167 | PF01111 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 162 | 168 | PF00134 | 0.675 |
DOC_MAPK_gen_1 | 411 | 419 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 450 | 458 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 471 | 479 | PF00069 | 0.619 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 443 | 446 | PF00568 | 0.585 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.527 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.675 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.399 |
LIG_14-3-3_CanoR_1 | 149 | 158 | PF00244 | 0.809 |
LIG_14-3-3_CanoR_1 | 202 | 208 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 497 | 501 | PF00244 | 0.546 |
LIG_APCC_ABBA_1 | 527 | 532 | PF00400 | 0.619 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.684 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.619 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.664 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.667 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.717 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.457 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.612 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.580 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.504 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.504 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.591 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.618 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.494 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.671 |
LIG_LIR_Apic_2 | 442 | 446 | PF02991 | 0.574 |
LIG_LIR_Apic_2 | 540 | 545 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 464 | 475 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.660 |
LIG_MLH1_MIPbox_1 | 539 | 543 | PF16413 | 0.619 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.511 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.403 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.667 |
LIG_PCNA_yPIPBox_3 | 324 | 332 | PF02747 | 0.388 |
LIG_SH2_PTP2 | 474 | 477 | PF00017 | 0.619 |
LIG_SH2_SRC | 474 | 477 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 427 | 431 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.569 |
LIG_SH3_1 | 364 | 370 | PF00018 | 0.659 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.586 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.681 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.412 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.659 |
LIG_UBA3_1 | 290 | 295 | PF00899 | 0.600 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.699 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.802 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.601 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.613 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.526 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.487 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.637 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.755 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.694 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.690 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.756 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.678 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.729 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.482 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.546 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.792 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.647 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.729 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.759 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.770 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.690 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.670 |
MOD_GlcNHglycan | 428 | 432 | PF01048 | 0.516 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.346 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.633 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.758 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.693 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.804 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.660 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.692 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.717 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.770 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.664 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.463 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.485 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.751 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.456 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.632 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.627 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.749 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.787 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.741 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.701 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.412 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.457 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.575 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.830 |
MOD_NEK2_2 | 166 | 171 | PF00069 | 0.404 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.655 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.740 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.563 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.588 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.478 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.651 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.546 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.627 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.555 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.542 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.530 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.627 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.523 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.545 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.619 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.534 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.720 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.582 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.509 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.487 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.601 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.625 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.399 |
MOD_SUMO_for_1 | 294 | 297 | PF00179 | 0.622 |
TRG_DiLeu_BaEn_2 | 525 | 531 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_4 | 322 | 328 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 389 | 394 | PF01217 | 0.499 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.569 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.546 |
TRG_NES_CRM1_1 | 181 | 195 | PF08389 | 0.511 |
TRG_NES_CRM1_1 | 280 | 293 | PF08389 | 0.605 |
TRG_NES_CRM1_1 | 329 | 343 | PF08389 | 0.444 |
TRG_NES_CRM1_1 | 448 | 462 | PF08389 | 0.530 |
TRG_NES_CRM1_1 | 519 | 532 | PF08389 | 0.563 |
TRG_NLS_MonoCore_2 | 10 | 15 | PF00514 | 0.620 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.689 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 459 | 463 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I883 | Leptomonas seymouri | 45% | 100% |
A0A3Q8ICC8 | Leishmania donovani | 89% | 100% |
A4HCE1 | Leishmania braziliensis | 72% | 99% |
A4HZW5 | Leishmania infantum | 88% | 100% |
Q4QBQ6 | Leishmania major | 86% | 99% |