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: A4HZW5
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 | 238 | 242 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.648 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.278 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.260 |
DEG_APCC_DBOX_1 | 448 | 456 | PF00400 | 0.475 |
DEG_ODPH_VHL_1 | 367 | 380 | PF01847 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 161 | 167 | PF00134 | 0.566 |
DOC_MAPK_gen_1 | 410 | 418 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 449 | 457 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 470 | 478 | PF00069 | 0.529 |
DOC_PP2B_LxvP_1 | 161 | 164 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.430 |
DOC_PP4_FxxP_1 | 264 | 267 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 442 | 445 | PF00568 | 0.428 |
DOC_PP4_FxxP_1 | 541 | 544 | PF00568 | 0.422 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.547 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 148 | 157 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 496 | 500 | PF00244 | 0.482 |
LIG_APCC_ABBA_1 | 526 | 531 | PF00400 | 0.529 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.661 |
LIG_BRCT_BRCA1_1 | 538 | 542 | PF00533 | 0.489 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.550 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.710 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.611 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.529 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.518 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.439 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.459 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.483 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.569 |
LIG_Integrin_isoDGR_2 | 351 | 353 | PF01839 | 0.614 |
LIG_LIR_Apic_2 | 538 | 544 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 284 | 295 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 463 | 474 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 472 | 476 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.637 |
LIG_MLH1_MIPbox_1 | 538 | 542 | PF16413 | 0.489 |
LIG_NRBOX | 245 | 251 | PF00104 | 0.426 |
LIG_NRBOX | 325 | 331 | PF00104 | 0.395 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.546 |
LIG_SH2_PTP2 | 473 | 476 | PF00017 | 0.529 |
LIG_SH2_SRC | 473 | 476 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 426 | 430 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.529 |
LIG_SH3_1 | 363 | 369 | PF00018 | 0.520 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.643 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.671 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.520 |
LIG_UBA3_1 | 289 | 294 | PF00899 | 0.471 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.658 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.679 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.642 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.529 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.548 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.398 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.550 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.631 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.617 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.618 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.631 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.377 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.497 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.754 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.618 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.728 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.705 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.653 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.428 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.571 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.275 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.565 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.628 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.622 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.550 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.679 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.584 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.558 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.613 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.757 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.547 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.371 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.423 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.796 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.642 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.671 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.628 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.636 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.347 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.402 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.567 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.692 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.577 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.631 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.495 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.558 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.547 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.475 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.492 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.475 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.482 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.511 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.492 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.420 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.529 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.463 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.631 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.369 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.564 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.806 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.492 |
MOD_SUMO_for_1 | 293 | 296 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 286 | 295 | PF00179 | 0.339 |
MOD_SUMO_rev_2 | 307 | 316 | PF00179 | 0.559 |
TRG_DiLeu_BaEn_2 | 524 | 530 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_4 | 321 | 327 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 388 | 393 | PF01217 | 0.396 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.478 |
TRG_NES_CRM1_1 | 180 | 194 | PF08389 | 0.407 |
TRG_NES_CRM1_1 | 279 | 292 | PF08389 | 0.474 |
TRG_NES_CRM1_1 | 328 | 342 | PF08389 | 0.404 |
TRG_NES_CRM1_1 | 447 | 461 | PF08389 | 0.483 |
TRG_NES_CRM1_1 | 518 | 531 | PF08389 | 0.495 |
TRG_NLS_MonoCore_2 | 10 | 15 | PF00514 | 0.501 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 458 | 462 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I883 | Leptomonas seymouri | 42% | 100% |
A0A3Q8ICC8 | Leishmania donovani | 99% | 100% |
A4HCE1 | Leishmania braziliensis | 73% | 99% |
E9AVS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QBQ6 | Leishmania major | 90% | 99% |