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:0005682 | U5 snRNP | 5 | 2 |
GO:0005684 | U2-type spliceosomal complex | 4 | 2 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 2 |
GO:0071020 | post-spliceosomal complex | 4 | 2 |
GO:0071021 | U2-type post-spliceosomal complex | 5 | 2 |
GO:0097525 | spliceosomal snRNP complex | 4 | 2 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 2 |
GO:0120114 | Sm-like protein family complex | 2 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
Related structures:
AlphaFold database: Q4QBQ6
Term | Name | Level | Count |
---|---|---|---|
GO:0000350 | generation of catalytic spliceosome for second transesterification step | 7 | 2 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006396 | RNA processing | 6 | 5 |
GO:0006397 | mRNA processing | 7 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0008380 | RNA splicing | 7 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0016071 | mRNA metabolic process | 6 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.289 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.290 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.405 |
CLV_Separin_Metazoa | 324 | 328 | PF03568 | 0.289 |
DEG_APCC_DBOX_1 | 444 | 452 | PF00400 | 0.469 |
DEG_COP1_1 | 156 | 165 | PF00400 | 0.479 |
DEG_COP1_1 | 211 | 219 | PF00400 | 0.496 |
DEG_ODPH_VHL_1 | 363 | 376 | PF01847 | 0.481 |
DEG_SCF_FBW7_1 | 52 | 57 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.489 |
DEG_SPOP_SBC_1 | 240 | 244 | PF00917 | 0.470 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 406 | 414 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 445 | 453 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 466 | 474 | PF00069 | 0.551 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 260 | 263 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.404 |
DOC_PP4_FxxP_1 | 537 | 540 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.532 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 144 | 153 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 197 | 203 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 349 | 358 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 492 | 496 | PF00244 | 0.469 |
LIG_APCC_ABBA_1 | 522 | 527 | PF00400 | 0.516 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.585 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.565 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.609 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.648 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.500 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.595 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.455 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.456 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.481 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.399 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.569 |
LIG_Integrin_isoDGR_2 | 347 | 349 | PF01839 | 0.590 |
LIG_LIR_Apic_2 | 437 | 441 | PF02991 | 0.350 |
LIG_LIR_Apic_2 | 534 | 540 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 280 | 291 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 459 | 470 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 468 | 472 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.538 |
LIG_MLH1_MIPbox_1 | 534 | 538 | PF16413 | 0.461 |
LIG_NRBOX | 321 | 327 | PF00104 | 0.386 |
LIG_NRBOX | 331 | 337 | PF00104 | 0.321 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.539 |
LIG_PCNA_yPIPBox_3 | 319 | 327 | PF02747 | 0.311 |
LIG_SH2_PTP2 | 469 | 472 | PF00017 | 0.516 |
LIG_SH2_SRC | 469 | 472 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 422 | 426 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.611 |
LIG_SH3_1 | 359 | 365 | PF00018 | 0.545 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.576 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.682 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.545 |
LIG_UBA3_1 | 285 | 290 | PF00899 | 0.473 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.665 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.560 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.526 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.440 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.520 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.517 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.415 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.636 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.521 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.547 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.642 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.624 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.386 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.471 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.742 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.537 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.636 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.682 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.640 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.674 |
MOD_GlcNHglycan | 423 | 427 | PF01048 | 0.417 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.269 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.580 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.657 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.589 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.588 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.561 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.597 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.735 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.546 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.628 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.474 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.389 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.761 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.625 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.659 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.625 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.515 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.594 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.432 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.683 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.530 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.573 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.627 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.484 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.475 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.532 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.516 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.469 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.537 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.490 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.469 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.455 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.511 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.545 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.492 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.403 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.609 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.458 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.606 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.529 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.451 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.506 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.763 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.592 |
MOD_SUMO_for_1 | 289 | 292 | PF00179 | 0.497 |
TRG_DiLeu_BaEn_2 | 520 | 526 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_4 | 317 | 323 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 384 | 389 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.611 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.518 |
TRG_NES_CRM1_1 | 176 | 190 | PF08389 | 0.412 |
TRG_NES_CRM1_1 | 275 | 288 | PF08389 | 0.472 |
TRG_NES_CRM1_1 | 324 | 338 | PF08389 | 0.395 |
TRG_NES_CRM1_1 | 443 | 457 | PF08389 | 0.455 |
TRG_NES_CRM1_1 | 514 | 527 | PF08389 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I883 | Leptomonas seymouri | 44% | 100% |
A0A3Q8ICC8 | Leishmania donovani | 90% | 99% |
A4HCE1 | Leishmania braziliensis | 73% | 100% |
A4HZW5 | Leishmania infantum | 90% | 99% |
E9AVS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |