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: 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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I872
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 1 |
GO:0005198 | structural molecule activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.540 |
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.487 |
CLV_PCSK_FUR_1 | 302 | 306 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.393 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.566 |
CLV_PCSK_PC7_1 | 344 | 350 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.732 |
DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.555 |
DEG_COP1_1 | 582 | 591 | PF00400 | 0.433 |
DOC_CYCLIN_RxL_1 | 120 | 132 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 618 | 624 | PF00069 | 0.610 |
DOC_MAPK_gen_1 | 642 | 648 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 174 | 183 | PF00069 | 0.471 |
DOC_MAPK_RevD_3 | 605 | 619 | PF00069 | 0.387 |
DOC_PP1_RVXF_1 | 222 | 228 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 517 | 523 | PF00149 | 0.407 |
DOC_PP2B_LxvP_1 | 455 | 458 | PF13499 | 0.553 |
DOC_PP2B_LxvP_1 | 581 | 584 | PF13499 | 0.398 |
DOC_PP2B_LxvP_1 | 586 | 589 | PF13499 | 0.478 |
DOC_PP4_FxxP_1 | 227 | 230 | PF00568 | 0.649 |
DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.662 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.626 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.433 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 26 | 36 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 303 | 309 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 618 | 623 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 642 | 647 | PF00244 | 0.567 |
LIG_Actin_WH2_2 | 363 | 380 | PF00022 | 0.383 |
LIG_APCC_ABBAyCdc20_2 | 137 | 143 | PF00400 | 0.530 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.747 |
LIG_BIR_III_4 | 51 | 55 | PF00653 | 0.532 |
LIG_Clathr_ClatBox_1 | 566 | 570 | PF01394 | 0.428 |
LIG_Clathr_ClatBox_1 | 69 | 73 | PF01394 | 0.527 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.636 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.655 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.574 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.445 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.644 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.612 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.418 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.470 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.476 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.496 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.550 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.549 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.754 |
LIG_LIR_Gen_1 | 395 | 402 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 502 | 508 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.533 |
LIG_MYND_1 | 230 | 234 | PF01753 | 0.602 |
LIG_Pex14_2 | 227 | 231 | PF04695 | 0.478 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.583 |
LIG_PTAP_UEV_1 | 462 | 467 | PF05743 | 0.532 |
LIG_PTAP_UEV_1 | 588 | 593 | PF05743 | 0.429 |
LIG_SH2_PTP2 | 327 | 330 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.526 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.497 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.618 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.626 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.568 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.591 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.460 |
LIG_SUMO_SIM_par_1 | 603 | 608 | PF11976 | 0.386 |
LIG_TRAF2_1 | 331 | 334 | PF00917 | 0.456 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.431 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.629 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.486 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.526 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.670 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.572 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.583 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.578 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.540 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.632 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.606 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.585 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.469 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.593 |
MOD_Cter_Amidation | 265 | 268 | PF01082 | 0.664 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.576 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.438 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.406 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.524 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.568 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.490 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.548 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.614 |
MOD_GlcNHglycan | 488 | 492 | PF01048 | 0.690 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.344 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.504 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.539 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.697 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.506 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.566 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.596 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.386 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.629 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.698 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.566 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.448 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.560 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.386 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.399 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.449 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.432 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.577 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.618 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.775 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.657 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.631 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.350 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.438 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.539 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.471 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.522 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.470 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.443 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.587 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.597 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.472 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.510 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.449 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.325 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.579 |
MOD_PKA_1 | 255 | 261 | PF00069 | 0.581 |
MOD_PKA_1 | 304 | 310 | PF00069 | 0.593 |
MOD_PKA_1 | 618 | 624 | PF00069 | 0.422 |
MOD_PKA_1 | 642 | 648 | PF00069 | 0.412 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.622 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.569 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.664 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.439 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.444 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.462 |
MOD_PKA_2 | 641 | 647 | PF00069 | 0.576 |
MOD_PKB_1 | 302 | 310 | PF00069 | 0.351 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.313 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.652 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.492 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.510 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.460 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.319 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.374 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.622 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.291 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.770 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.617 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.425 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.629 |
TRG_DiLeu_BaEn_1 | 65 | 70 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_2 | 340 | 346 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 474 | 479 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5A1 | Leptomonas seymouri | 46% | 100% |
A0A1X0NRK2 | Trypanosomatidae | 31% | 100% |
A0A3Q8IG27 | Leishmania donovani | 100% | 100% |
A4HKP1 | Leishmania braziliensis | 73% | 100% |
D0AAE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B330 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q524 | Leishmania major | 90% | 100% |
V5AUP9 | Trypanosoma cruzi | 32% | 100% |