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: A0A3S7WYC4
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 | 155 | 159 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 21 | 25 | PF00656 | 0.647 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.667 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.561 |
DEG_SPOP_SBC_1 | 106 | 110 | PF00917 | 0.611 |
DEG_SPOP_SBC_1 | 209 | 213 | PF00917 | 0.547 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 282 | 286 | PF00917 | 0.669 |
DEG_SPOP_SBC_1 | 411 | 415 | PF00917 | 0.640 |
DOC_CDC14_PxL_1 | 35 | 43 | PF14671 | 0.568 |
DOC_MAPK_gen_1 | 526 | 535 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 565 | 572 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 370 | 376 | PF00149 | 0.461 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.631 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.778 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.544 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.409 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 188 | 195 | PF00244 | 0.808 |
LIG_14-3-3_CanoR_1 | 260 | 269 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 321 | 329 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 451 | 460 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 87 | 93 | PF00244 | 0.743 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.694 |
LIG_BIR_III_2 | 9 | 13 | PF00653 | 0.675 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.666 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.679 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.598 |
LIG_Clathr_ClatBox_1 | 514 | 518 | PF01394 | 0.488 |
LIG_EVH1_1 | 431 | 435 | PF00568 | 0.583 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.680 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.483 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.495 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.656 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.503 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.470 |
LIG_LIR_Gen_1 | 218 | 229 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.448 |
LIG_MLH1_MIPbox_1 | 109 | 113 | PF16413 | 0.667 |
LIG_MYND_1 | 429 | 433 | PF01753 | 0.639 |
LIG_PAM2_1 | 433 | 445 | PF00658 | 0.551 |
LIG_PCNA_yPIPBox_3 | 250 | 261 | PF02747 | 0.506 |
LIG_REV1ctd_RIR_1 | 373 | 379 | PF16727 | 0.464 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.516 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.620 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.688 |
LIG_SUMO_SIM_par_1 | 531 | 537 | PF11976 | 0.424 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.535 |
MOD_CDK_SPxK_1 | 81 | 87 | PF00069 | 0.573 |
MOD_CDK_SPxxK_3 | 81 | 88 | PF00069 | 0.673 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.701 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.693 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.759 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.567 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.697 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.599 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.731 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.708 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.619 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.617 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.695 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.581 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.590 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.502 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.440 |
MOD_Cter_Amidation | 336 | 339 | PF01082 | 0.521 |
MOD_Cter_Amidation | 461 | 464 | PF01082 | 0.407 |
MOD_DYRK1A_RPxSP_1 | 88 | 92 | PF00069 | 0.563 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.673 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.763 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.728 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.737 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.746 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.602 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.744 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.698 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.616 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.486 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.589 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.655 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.604 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.756 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.682 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.662 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.648 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.683 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.635 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.735 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.823 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.688 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.688 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.650 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.643 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.661 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.712 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.532 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.789 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.413 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.750 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.668 |
MOD_LATS_1 | 13 | 19 | PF00433 | 0.702 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.709 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.719 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.619 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.367 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.572 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.705 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.567 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.395 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.498 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.478 |
MOD_NEK2_2 | 494 | 499 | PF00069 | 0.735 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.645 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.643 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.739 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.643 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.449 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.664 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.402 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.554 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.440 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.392 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.709 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.750 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.693 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.558 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.639 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.670 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.672 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.700 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.526 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 338 | 343 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.619 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD00 | Leptomonas seymouri | 47% | 100% |
A0A3R7R9R9 | Trypanosoma rangeli | 35% | 100% |
A4HDD7 | Leishmania braziliensis | 73% | 97% |
A4I0R8 | Leishmania infantum | 99% | 100% |
D0A749 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AWS0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QAQ4 | Leishmania major | 90% | 100% |