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: A0A3Q8ICC8
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 | 237 | 241 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.277 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.277 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.283 |
DEG_APCC_DBOX_1 | 447 | 455 | PF00400 | 0.489 |
DEG_ODPH_VHL_1 | 366 | 379 | PF01847 | 0.511 |
DOC_CYCLIN_yCln2_LP_2 | 160 | 166 | PF00134 | 0.587 |
DOC_MAPK_gen_1 | 409 | 417 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 448 | 456 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 469 | 477 | PF00069 | 0.535 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 263 | 266 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 441 | 444 | PF00568 | 0.490 |
DOC_PP4_FxxP_1 | 540 | 543 | PF00568 | 0.422 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.563 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 147 | 156 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 200 | 206 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 495 | 499 | PF00244 | 0.477 |
LIG_APCC_ABBA_1 | 525 | 530 | PF00400 | 0.535 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.490 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.570 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.623 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.621 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.559 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.520 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.441 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.472 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.496 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.591 |
LIG_Integrin_isoDGR_2 | 350 | 352 | PF01839 | 0.632 |
LIG_LIR_Apic_2 | 537 | 543 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 462 | 473 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 471 | 475 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.583 |
LIG_MLH1_MIPbox_1 | 537 | 541 | PF16413 | 0.490 |
LIG_NRBOX | 244 | 250 | PF00104 | 0.444 |
LIG_NRBOX | 324 | 330 | PF00104 | 0.404 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.569 |
LIG_SH2_PTP2 | 472 | 475 | PF00017 | 0.535 |
LIG_SH2_SRC | 472 | 475 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 211 | 215 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.477 |
LIG_SH3_1 | 362 | 368 | PF00018 | 0.605 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.585 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.651 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.605 |
LIG_UBA3_1 | 288 | 293 | PF00899 | 0.482 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.593 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.698 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.538 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.433 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.510 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.413 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.565 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.659 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.595 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.640 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.652 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.383 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.493 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.759 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.605 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.658 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.724 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.664 |
MOD_GlcNHglycan | 426 | 430 | PF01048 | 0.431 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.626 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.277 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.595 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.594 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.601 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.691 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.609 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.559 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.605 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.770 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.573 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.440 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.404 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.716 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.658 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.690 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.647 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.614 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.452 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.415 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.457 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.717 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.542 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.649 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.499 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.467 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.563 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.477 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.505 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.487 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.462 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.506 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.505 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.427 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.559 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.465 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.634 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.392 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.572 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.732 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 285 | 294 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 306 | 315 | PF00179 | 0.575 |
TRG_DiLeu_BaEn_2 | 523 | 529 | PF01217 | 0.477 |
TRG_DiLeu_BaEn_4 | 320 | 326 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 503 | 506 | PF00400 | 0.477 |
TRG_NES_CRM1_1 | 179 | 193 | PF08389 | 0.418 |
TRG_NES_CRM1_1 | 278 | 291 | PF08389 | 0.485 |
TRG_NES_CRM1_1 | 327 | 341 | PF08389 | 0.414 |
TRG_NES_CRM1_1 | 446 | 460 | PF08389 | 0.462 |
TRG_NES_CRM1_1 | 517 | 530 | PF08389 | 0.499 |
TRG_NLS_MonoCore_2 | 10 | 15 | PF00514 | 0.528 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 395 | 399 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I883 | Leptomonas seymouri | 42% | 100% |
A4HCE1 | Leishmania braziliensis | 74% | 99% |
A4HZW5 | Leishmania infantum | 99% | 100% |
E9AVS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QBQ6 | Leishmania major | 90% | 99% |