Translation, 4E-interacting 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pescher et al. (upgregulation) | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
|
Lahav et al. - mRNA
- Protein
|
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006417 | regulation of translation | 6 | 1 |
| GO:0009889 | regulation of biosynthetic process | 4 | 1 |
| GO:0010468 | regulation of gene expression | 5 | 1 |
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
| GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
| GO:0019222 | regulation of metabolic process | 3 | 1 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
| GO:0034248 | regulation of amide metabolic process | 5 | 1 |
| GO:0050789 | regulation of biological process | 2 | 1 |
| GO:0050794 | regulation of cellular process | 3 | 1 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
| GO:0051246 | regulation of protein metabolic process | 5 | 1 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
| GO:0065007 | biological regulation | 1 | 1 |
| GO:0080090 | regulation of primary metabolic process | 4 | 1 |
| GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0045182 | translation regulator activity | 1 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.619 |
| CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.661 |
| CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.558 |
| CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.659 |
| CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.502 |
| CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.626 |
| CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.661 |
| CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.541 |
| CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.646 |
| CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.626 |
| CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.541 |
| CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.646 |
| CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.570 |
| CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.503 |
| CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.707 |
| CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.659 |
| CLV_Separin_Metazoa | 12 | 16 | PF03568 | 0.624 |
| CLV_Separin_Metazoa | 28 | 32 | PF03568 | 0.393 |
| DEG_APCC_DBOX_1 | 9 | 17 | PF00400 | 0.526 |
| DEG_COP1_1 | 479 | 489 | PF00400 | 0.759 |
| DEG_SCF_FBW7_1 | 294 | 301 | PF00400 | 0.620 |
| DEG_SCF_FBW7_1 | 449 | 456 | PF00400 | 0.679 |
| DEG_SIAH_1 | 289 | 297 | PF03145 | 0.687 |
| DEG_SPOP_SBC_1 | 283 | 287 | PF00917 | 0.684 |
| DEG_SPOP_SBC_1 | 366 | 370 | PF00917 | 0.711 |
| DOC_CKS1_1 | 295 | 300 | PF01111 | 0.666 |
| DOC_CKS1_1 | 450 | 455 | PF01111 | 0.740 |
| DOC_CYCLIN_yClb3_PxF_3 | 557 | 563 | PF00134 | 0.759 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 191 | 199 | PF00134 | 0.564 |
| DOC_CYCLIN_yCln2_LP_2 | 713 | 719 | PF00134 | 0.630 |
| DOC_MAPK_gen_1 | 31 | 38 | PF00069 | 0.707 |
| DOC_PP2B_LxvP_1 | 627 | 630 | PF13499 | 0.703 |
| DOC_PP2B_LxvP_1 | 713 | 716 | PF13499 | 0.632 |
| DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.598 |
| DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.675 |
| DOC_PP4_FxxP_1 | 399 | 402 | PF00568 | 0.646 |
| DOC_PP4_FxxP_1 | 563 | 566 | PF00568 | 0.660 |
| DOC_PP4_FxxP_1 | 576 | 579 | PF00568 | 0.676 |
| DOC_PP4_FxxP_1 | 726 | 729 | PF00568 | 0.535 |
| DOC_PP4_FxxP_1 | 744 | 747 | PF00568 | 0.381 |
| DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.686 |
| DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.602 |
| DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.646 |
| DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.559 |
| DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.410 |
| DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.706 |
| DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.732 |
| DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.552 |
| DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.623 |
| DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.751 |
| DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.718 |
| DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.584 |
| DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.716 |
| DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.650 |
| DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.693 |
| DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.665 |
| DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.642 |
| DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.591 |
| DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.609 |
| DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.658 |
| DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.744 |
| DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.605 |
| DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.767 |
| DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.755 |
| DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.679 |
| DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.765 |
| LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.646 |
| LIG_14-3-3_CanoR_1 | 242 | 249 | PF00244 | 0.615 |
| LIG_BIR_III_2 | 343 | 347 | PF00653 | 0.698 |
| LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.595 |
| LIG_EH_1 | 774 | 778 | PF12763 | 0.716 |
| LIG_eIF4E_1 | 8 | 14 | PF01652 | 0.522 |
| LIG_EVH1_1 | 627 | 631 | PF00568 | 0.702 |
| LIG_FHA_1 | 216 | 222 | PF00498 | 0.558 |
| LIG_FHA_1 | 524 | 530 | PF00498 | 0.672 |
| LIG_FHA_1 | 690 | 696 | PF00498 | 0.770 |
| LIG_FHA_2 | 160 | 166 | PF00498 | 0.658 |
| LIG_FHA_2 | 205 | 211 | PF00498 | 0.492 |
| LIG_FHA_2 | 227 | 233 | PF00498 | 0.693 |
| LIG_FHA_2 | 250 | 256 | PF00498 | 0.685 |
| LIG_FHA_2 | 528 | 534 | PF00498 | 0.667 |
| LIG_FHA_2 | 7 | 13 | PF00498 | 0.530 |
| LIG_LIR_Apic_2 | 144 | 149 | PF02991 | 0.606 |
| LIG_LIR_Apic_2 | 272 | 278 | PF02991 | 0.677 |
| LIG_LIR_Apic_2 | 398 | 402 | PF02991 | 0.645 |
| LIG_LIR_Gen_1 | 141 | 149 | PF02991 | 0.716 |
| LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.630 |
| LIG_MLH1_MIPbox_1 | 240 | 244 | PF16413 | 0.595 |
| LIG_MYND_1 | 693 | 697 | PF01753 | 0.769 |
| LIG_NRBOX | 494 | 500 | PF00104 | 0.547 |
| LIG_NRP_CendR_1 | 790 | 791 | PF00754 | 0.702 |
| LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.614 |
| LIG_SH2_STAT5 | 725 | 728 | PF00017 | 0.599 |
| LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.526 |
| LIG_SH3_3 | 259 | 265 | PF00018 | 0.624 |
| LIG_SH3_3 | 349 | 355 | PF00018 | 0.684 |
| LIG_SH3_3 | 35 | 41 | PF00018 | 0.626 |
| LIG_SH3_3 | 398 | 404 | PF00018 | 0.733 |
| LIG_SH3_3 | 406 | 412 | PF00018 | 0.621 |
| LIG_SH3_3 | 414 | 420 | PF00018 | 0.509 |
| LIG_SH3_3 | 447 | 453 | PF00018 | 0.732 |
| LIG_SH3_3 | 461 | 467 | PF00018 | 0.694 |
| LIG_SH3_3 | 507 | 513 | PF00018 | 0.684 |
| LIG_SH3_3 | 554 | 560 | PF00018 | 0.761 |
| LIG_SH3_3 | 563 | 569 | PF00018 | 0.600 |
| LIG_SH3_3 | 580 | 586 | PF00018 | 0.654 |
| LIG_SH3_3 | 614 | 620 | PF00018 | 0.751 |
| LIG_SH3_3 | 623 | 629 | PF00018 | 0.590 |
| LIG_SH3_3 | 630 | 636 | PF00018 | 0.452 |
| LIG_SH3_3 | 668 | 674 | PF00018 | 0.718 |
| LIG_SH3_3 | 691 | 697 | PF00018 | 0.716 |
| LIG_SH3_3 | 704 | 710 | PF00018 | 0.539 |
| LIG_SH3_3 | 770 | 776 | PF00018 | 0.715 |
| LIG_SUMO_SIM_anti_2 | 494 | 499 | PF11976 | 0.570 |
| LIG_SUMO_SIM_par_1 | 34 | 40 | PF11976 | 0.625 |
| LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.568 |
| LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.625 |
| MOD_CK1_1 | 103 | 109 | PF00069 | 0.652 |
| MOD_CK1_1 | 281 | 287 | PF00069 | 0.617 |
| MOD_CK1_1 | 313 | 319 | PF00069 | 0.703 |
| MOD_CK1_1 | 326 | 332 | PF00069 | 0.503 |
| MOD_CK1_1 | 357 | 363 | PF00069 | 0.738 |
| MOD_CK1_1 | 384 | 390 | PF00069 | 0.714 |
| MOD_CK1_1 | 479 | 485 | PF00069 | 0.616 |
| MOD_CK1_1 | 515 | 521 | PF00069 | 0.668 |
| MOD_CK1_1 | 57 | 63 | PF00069 | 0.695 |
| MOD_CK1_1 | 589 | 595 | PF00069 | 0.686 |
| MOD_CK1_1 | 64 | 70 | PF00069 | 0.629 |
| MOD_CK1_1 | 95 | 101 | PF00069 | 0.654 |
| MOD_CK2_1 | 159 | 165 | PF00069 | 0.667 |
| MOD_CK2_1 | 204 | 210 | PF00069 | 0.488 |
| MOD_CK2_1 | 249 | 255 | PF00069 | 0.683 |
| MOD_CK2_1 | 527 | 533 | PF00069 | 0.702 |
| MOD_CK2_1 | 6 | 12 | PF00069 | 0.594 |
| MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.654 |
| MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.506 |
| MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.569 |
| MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.617 |
| MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.664 |
| MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.611 |
| MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.682 |
| MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.732 |
| MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.659 |
| MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.737 |
| MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.695 |
| MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.638 |
| MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.548 |
| MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.685 |
| MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.688 |
| MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.763 |
| MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.674 |
| MOD_GSK3_1 | 130 | 137 | PF00069 | 0.727 |
| MOD_GSK3_1 | 238 | 245 | PF00069 | 0.592 |
| MOD_GSK3_1 | 256 | 263 | PF00069 | 0.605 |
| MOD_GSK3_1 | 267 | 274 | PF00069 | 0.609 |
| MOD_GSK3_1 | 277 | 284 | PF00069 | 0.631 |
| MOD_GSK3_1 | 290 | 297 | PF00069 | 0.620 |
| MOD_GSK3_1 | 309 | 316 | PF00069 | 0.489 |
| MOD_GSK3_1 | 319 | 326 | PF00069 | 0.557 |
| MOD_GSK3_1 | 331 | 338 | PF00069 | 0.498 |
| MOD_GSK3_1 | 357 | 364 | PF00069 | 0.735 |
| MOD_GSK3_1 | 377 | 384 | PF00069 | 0.436 |
| MOD_GSK3_1 | 391 | 398 | PF00069 | 0.573 |
| MOD_GSK3_1 | 424 | 431 | PF00069 | 0.685 |
| MOD_GSK3_1 | 434 | 441 | PF00069 | 0.633 |
| MOD_GSK3_1 | 449 | 456 | PF00069 | 0.636 |
| MOD_GSK3_1 | 476 | 483 | PF00069 | 0.639 |
| MOD_GSK3_1 | 484 | 491 | PF00069 | 0.625 |
| MOD_GSK3_1 | 501 | 508 | PF00069 | 0.645 |
| MOD_GSK3_1 | 515 | 522 | PF00069 | 0.731 |
| MOD_GSK3_1 | 523 | 530 | PF00069 | 0.552 |
| MOD_GSK3_1 | 548 | 555 | PF00069 | 0.715 |
| MOD_GSK3_1 | 57 | 64 | PF00069 | 0.705 |
| MOD_GSK3_1 | 585 | 592 | PF00069 | 0.681 |
| MOD_GSK3_1 | 639 | 646 | PF00069 | 0.711 |
| MOD_GSK3_1 | 65 | 72 | PF00069 | 0.623 |
| MOD_GSK3_1 | 94 | 101 | PF00069 | 0.646 |
| MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.635 |
| MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.638 |
| MOD_N-GLC_1 | 684 | 689 | PF02516 | 0.765 |
| MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.719 |
| MOD_NEK2_1 | 171 | 176 | PF00069 | 0.510 |
| MOD_NEK2_1 | 320 | 325 | PF00069 | 0.629 |
| MOD_NEK2_1 | 331 | 336 | PF00069 | 0.516 |
| MOD_NEK2_1 | 505 | 510 | PF00069 | 0.681 |
| MOD_NEK2_1 | 54 | 59 | PF00069 | 0.733 |
| MOD_NEK2_1 | 63 | 68 | PF00069 | 0.633 |
| MOD_NEK2_2 | 3 | 8 | PF00069 | 0.576 |
| MOD_NEK2_2 | 310 | 315 | PF00069 | 0.639 |
| MOD_NEK2_2 | 747 | 752 | PF00069 | 0.639 |
| MOD_PIKK_1 | 300 | 306 | PF00454 | 0.690 |
| MOD_PIKK_1 | 354 | 360 | PF00454 | 0.749 |
| MOD_PIKK_1 | 410 | 416 | PF00454 | 0.554 |
| MOD_PIKK_1 | 443 | 449 | PF00454 | 0.628 |
| MOD_PIKK_1 | 457 | 463 | PF00454 | 0.723 |
| MOD_PIKK_1 | 523 | 529 | PF00454 | 0.758 |
| MOD_PIKK_1 | 639 | 645 | PF00454 | 0.666 |
| MOD_PKA_2 | 171 | 177 | PF00069 | 0.537 |
| MOD_PKA_2 | 215 | 221 | PF00069 | 0.454 |
| MOD_PKA_2 | 477 | 483 | PF00069 | 0.682 |
| MOD_PKB_1 | 240 | 248 | PF00069 | 0.608 |
| MOD_Plk_2-3 | 215 | 221 | PF00069 | 0.668 |
| MOD_Plk_4 | 290 | 296 | PF00069 | 0.765 |
| MOD_Plk_4 | 413 | 419 | PF00069 | 0.775 |
| MOD_Plk_4 | 501 | 507 | PF00069 | 0.666 |
| MOD_Plk_4 | 533 | 539 | PF00069 | 0.563 |
| MOD_Plk_4 | 54 | 60 | PF00069 | 0.744 |
| MOD_Plk_4 | 747 | 753 | PF00069 | 0.547 |
| MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.668 |
| MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.736 |
| MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.592 |
| MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.610 |
| MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.660 |
| MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.747 |
| MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.606 |
| MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.769 |
| MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.757 |
| MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.681 |
| MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.767 |
| MOD_SUMO_for_1 | 202 | 205 | PF00179 | 0.680 |
| TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.643 |
| TRG_DiLeu_BaLyEn_6 | 570 | 575 | PF01217 | 0.653 |
| TRG_DiLeu_LyEn_5 | 220 | 225 | PF01217 | 0.643 |
| TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.623 |
| TRG_ER_diArg_1 | 239 | 242 | PF00400 | 0.536 |
| TRG_ER_diArg_1 | 744 | 746 | PF00400 | 0.502 |
| TRG_NES_CRM1_1 | 24 | 37 | PF08389 | 0.677 |
| TRG_NLS_MonoExtC_3 | 177 | 183 | PF00514 | 0.537 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HU08 | Leptomonas seymouri | 42% | 100% |
| A0A3S7X9R7 | Leishmania donovani | 99% | 100% |
| A4HN68 | Leishmania braziliensis | 73% | 100% |
| E9AFM3 | Leishmania major | 90% | 100% |
| E9B6S6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |