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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QAQ4
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 | 21 | 25 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.661 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.586 |
DEG_SCF_FBW7_1 | 213 | 218 | PF00400 | 0.551 |
DEG_SPOP_SBC_1 | 106 | 110 | PF00917 | 0.616 |
DEG_SPOP_SBC_1 | 181 | 185 | PF00917 | 0.502 |
DEG_SPOP_SBC_1 | 282 | 286 | PF00917 | 0.557 |
DEG_SPOP_SBC_1 | 3 | 7 | PF00917 | 0.525 |
DEG_SPOP_SBC_1 | 411 | 415 | PF00917 | 0.593 |
DOC_CDC14_PxL_1 | 35 | 43 | PF14671 | 0.594 |
DOC_CYCLIN_RxL_1 | 343 | 352 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 526 | 535 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 565 | 572 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 344 | 350 | PF00149 | 0.348 |
DOC_PP1_RVXF_1 | 370 | 376 | PF00149 | 0.467 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.639 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.727 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.541 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.443 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.814 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 260 | 270 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 451 | 460 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 87 | 94 | PF00244 | 0.660 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.672 |
LIG_BIR_III_2 | 9 | 13 | PF00653 | 0.686 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.682 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.646 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.604 |
LIG_Clathr_ClatBox_1 | 514 | 518 | PF01394 | 0.459 |
LIG_EVH1_1 | 431 | 435 | PF00568 | 0.591 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.546 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.718 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.546 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.494 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.489 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.665 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.495 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.443 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.434 |
LIG_LIR_Gen_1 | 218 | 229 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.516 |
LIG_MLH1_MIPbox_1 | 109 | 113 | PF16413 | 0.640 |
LIG_MYND_1 | 429 | 433 | PF01753 | 0.650 |
LIG_PAM2_1 | 433 | 445 | PF00658 | 0.556 |
LIG_PCNA_yPIPBox_3 | 250 | 261 | PF02747 | 0.465 |
LIG_REV1ctd_RIR_1 | 373 | 379 | PF16727 | 0.465 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.500 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.619 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.748 |
LIG_SUMO_SIM_par_1 | 531 | 537 | PF11976 | 0.433 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.551 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.667 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.627 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.581 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.753 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.613 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.766 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.633 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.601 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.779 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.604 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.497 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.445 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.370 |
MOD_Cter_Amidation | 336 | 339 | PF01082 | 0.539 |
MOD_Cter_Amidation | 461 | 464 | PF01082 | 0.411 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.575 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.659 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.623 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.787 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.693 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.694 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.706 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.623 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.599 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.679 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.701 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.691 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.619 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.526 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.529 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.669 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.695 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.755 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.663 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.673 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.727 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.517 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.833 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.637 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.582 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.668 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.793 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.669 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.496 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.564 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.753 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.678 |
MOD_LATS_1 | 13 | 19 | PF00433 | 0.712 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.606 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.676 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.562 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.546 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.429 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.457 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.419 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.450 |
MOD_NEK2_2 | 494 | 499 | PF00069 | 0.679 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.646 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.656 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.684 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.656 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.558 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.623 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.467 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.391 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.557 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.464 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.423 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.412 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.625 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.812 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.662 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.533 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.656 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.646 |
TRG_DiLeu_BaEn_1 | 510 | 515 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 343 | 348 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 444 | 449 | PF01217 | 0.347 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.534 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 338 | 343 | PF00026 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD00 | Leptomonas seymouri | 48% | 100% |
A0A3R7R9R9 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WYC4 | Leishmania donovani | 90% | 100% |
A4HDD7 | Leishmania braziliensis | 72% | 100% |
A4I0R8 | Leishmania infantum | 90% | 100% |
E9AWS0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |