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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HDD7
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 7 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 7 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006397 | mRNA processing | 7 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008380 | RNA splicing | 7 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0016071 | mRNA metabolic process | 6 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.570 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.618 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.727 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.452 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.548 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.512 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.695 |
DEG_SPOP_SBC_1 | 274 | 278 | PF00917 | 0.715 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.546 |
DEG_SPOP_SBC_1 | 82 | 86 | PF00917 | 0.531 |
DOC_CKS1_1 | 388 | 393 | PF01111 | 0.515 |
DOC_MAPK_gen_1 | 501 | 510 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 540 | 547 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 347 | 353 | PF00149 | 0.466 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.652 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.799 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.639 |
DOC_USP7_UBL2_3 | 441 | 445 | PF12436 | 0.408 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 90 | 99 | PF00244 | 0.711 |
LIG_BIR_III_2 | 6 | 10 | PF00653 | 0.671 |
LIG_BIR_III_4 | 124 | 128 | PF00653 | 0.543 |
LIG_BIR_III_4 | 129 | 133 | PF00653 | 0.527 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.654 |
LIG_Clathr_ClatBox_1 | 489 | 493 | PF01394 | 0.487 |
LIG_Clathr_ClatBox_1 | 531 | 535 | PF01394 | 0.306 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.456 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.337 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.496 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.517 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.668 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.540 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.498 |
LIG_LIR_Gen_1 | 210 | 221 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 351 | 355 | PF02991 | 0.450 |
LIG_MYND_1 | 406 | 410 | PF01753 | 0.658 |
LIG_PAM2_1 | 410 | 422 | PF00658 | 0.554 |
LIG_PTAP_UEV_1 | 390 | 395 | PF05743 | 0.519 |
LIG_REV1ctd_RIR_1 | 350 | 356 | PF16727 | 0.465 |
LIG_SH2_PTP2 | 219 | 222 | PF00017 | 0.548 |
LIG_SH2_STAT3 | 313 | 316 | PF00017 | 0.460 |
LIG_SH2_STAT3 | 360 | 363 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.633 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.571 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.738 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.615 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.537 |
LIG_UBA3_1 | 248 | 253 | PF00899 | 0.341 |
MOD_CDK_SPxxK_3 | 304 | 311 | PF00069 | 0.425 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.675 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.720 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.585 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.616 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.474 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.677 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.687 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.580 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.544 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.478 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.444 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.473 |
MOD_Cter_Amidation | 438 | 441 | PF01082 | 0.404 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.607 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.724 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.543 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.499 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.561 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.566 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.489 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.554 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.639 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.724 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.570 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.535 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.629 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.658 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.559 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.646 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.598 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.679 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.638 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.651 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.549 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.473 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.367 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.543 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.605 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.775 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.411 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.747 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.704 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.541 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.711 |
MOD_LATS_1 | 10 | 16 | PF00433 | 0.698 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.540 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.594 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.731 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.496 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.670 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.499 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.540 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.458 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.514 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.536 |
MOD_NEK2_2 | 348 | 353 | PF00069 | 0.482 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.726 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.506 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.718 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.453 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.374 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.543 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.479 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.431 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.706 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.541 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.345 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.444 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.455 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.396 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.555 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.768 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.616 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.696 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.684 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.650 |
TRG_DiLeu_BaEn_1 | 485 | 490 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.551 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 520 | 523 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 315 | 320 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.629 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD00 | Leptomonas seymouri | 46% | 100% |
A0A3R7R9R9 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WYC4 | Leishmania donovani | 73% | 96% |
A4I0R8 | Leishmania infantum | 73% | 96% |
D0A749 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AWS0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 97% |
Q4QAQ4 | Leishmania major | 72% | 100% |