Uncharacterized Protein, Uncharacterized
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: 5 |
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0005685 | U1 snRNP | 5 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071004 | U2-type prespliceosome | 5 | 1 |
GO:0071010 | prespliceosome | 4 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HX11
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.574 |
DEG_Kelch_Keap1_1 | 154 | 159 | PF01344 | 0.559 |
DEG_SPOP_SBC_1 | 337 | 341 | PF00917 | 0.740 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.810 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.643 |
DOC_CKS1_1 | 594 | 599 | PF01111 | 0.694 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.601 |
DOC_CYCLIN_RxL_1 | 102 | 110 | PF00134 | 0.663 |
DOC_CYCLIN_RxL_1 | 419 | 431 | PF00134 | 0.649 |
DOC_CYCLIN_RxL_1 | 75 | 84 | PF00134 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.715 |
DOC_CYCLIN_yCln2_LP_2 | 611 | 617 | PF00134 | 0.485 |
DOC_MAPK_DCC_7 | 299 | 309 | PF00069 | 0.638 |
DOC_PP1_RVXF_1 | 51 | 58 | PF00149 | 0.545 |
DOC_PP1_RVXF_1 | 76 | 83 | PF00149 | 0.574 |
DOC_PP2B_LxvP_1 | 271 | 274 | PF13499 | 0.795 |
DOC_PP2B_LxvP_1 | 611 | 614 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.786 |
DOC_PP4_MxPP_1 | 356 | 359 | PF00568 | 0.722 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.755 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 462 | 466 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 515 | 521 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 578 | 583 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.645 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.326 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.695 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.771 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.809 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.646 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.655 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.420 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.498 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.434 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.498 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.576 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.607 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.603 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.581 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.485 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.485 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.424 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.630 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.789 |
LIG_LIR_Apic_2 | 415 | 420 | PF02991 | 0.539 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 528 | 534 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 580 | 585 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 635 | 641 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 390 | 398 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.573 |
LIG_Pex14_1 | 391 | 395 | PF04695 | 0.457 |
LIG_SH2_GRB2like | 521 | 524 | PF00017 | 0.401 |
LIG_SH2_GRB2like | 572 | 575 | PF00017 | 0.444 |
LIG_SH2_GRB2like | 628 | 631 | PF00017 | 0.369 |
LIG_SH2_SRC | 466 | 469 | PF00017 | 0.444 |
LIG_SH2_SRC | 521 | 524 | PF00017 | 0.401 |
LIG_SH2_SRC | 628 | 631 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.565 |
LIG_SH3_2 | 420 | 425 | PF14604 | 0.666 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.735 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.701 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.751 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.721 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.664 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.733 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.808 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.756 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.561 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.634 |
LIG_SH3_4 | 586 | 593 | PF00018 | 0.629 |
LIG_SH3_CIN85_PxpxPR_1 | 262 | 267 | PF14604 | 0.567 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.569 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.553 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.482 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.683 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.779 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.593 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.491 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.738 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.553 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.568 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.546 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.738 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.719 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.485 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.485 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.424 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.583 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.582 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.733 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.730 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.619 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.550 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.664 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.706 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.738 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.803 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.669 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.790 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.806 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.657 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.643 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.679 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.679 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.647 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.659 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.736 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.660 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.575 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.756 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.525 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.627 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.466 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.280 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.750 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.390 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.444 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.620 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.374 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.686 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.706 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.751 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.636 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.637 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.650 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.714 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.580 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.574 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.532 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.678 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.657 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.553 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.617 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.409 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.791 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.485 |
MOD_PKB_1 | 79 | 87 | PF00069 | 0.588 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.685 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.600 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.747 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.787 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.728 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.643 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.667 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.666 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.707 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.717 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.823 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.535 |
MOD_SUMO_rev_2 | 18 | 25 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 222 | 232 | PF00179 | 0.587 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 78 | 83 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ37 | Leptomonas seymouri | 50% | 100% |
A0A3Q8IJ47 | Leishmania donovani | 98% | 100% |
A0A3R7LE31 | Trypanosoma rangeli | 34% | 98% |
A4H8P0 | Leishmania braziliensis | 73% | 93% |
C9ZVZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AQS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |
Q4QEQ3 | Leishmania major | 93% | 99% |
V5BML0 | Trypanosoma cruzi | 36% | 100% |