| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AHQ9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006417 | regulation of translation | 6 | 11 |
| GO:0006448 | regulation of translational elongation | 7 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0008152 | metabolic process | 1 | 11 |
| GO:0009058 | biosynthetic process | 2 | 11 |
| GO:0009889 | regulation of biosynthetic process | 4 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0010468 | regulation of gene expression | 5 | 11 |
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 11 |
| GO:0010608 | post-transcriptional regulation of gene expression | 6 | 11 |
| GO:0017182 | peptidyl-diphthamide metabolic process | 7 | 11 |
| GO:0017183 | peptidyl-diphthamide biosynthetic process from peptidyl-histidine | 4 | 11 |
| GO:0018193 | peptidyl-amino acid modification | 5 | 11 |
| GO:0018202 | peptidyl-histidine modification | 6 | 11 |
| GO:0019222 | regulation of metabolic process | 3 | 11 |
| GO:0019538 | protein metabolic process | 3 | 11 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 11 |
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 11 |
| GO:0034248 | regulation of amide metabolic process | 5 | 11 |
| GO:0036211 | protein modification process | 4 | 11 |
| GO:0043170 | macromolecule metabolic process | 3 | 11 |
| GO:0043412 | macromolecule modification | 4 | 11 |
| GO:0044237 | cellular metabolic process | 2 | 11 |
| GO:0044238 | primary metabolic process | 2 | 11 |
| GO:0044249 | cellular biosynthetic process | 3 | 11 |
| GO:0050789 | regulation of biological process | 2 | 11 |
| GO:0050794 | regulation of cellular process | 3 | 11 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 |
| GO:0051246 | regulation of protein metabolic process | 5 | 11 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 |
| GO:0065007 | biological regulation | 1 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 11 |
| GO:0080090 | regulation of primary metabolic process | 4 | 11 |
| GO:1900247 | regulation of cytoplasmic translational elongation | 8 | 11 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
| GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0016740 | transferase activity | 2 | 11 |
| GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 11 |
| GO:0090560 | 2-(3-amino-3-carboxypropyl)histidine synthase activity | 4 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.317 |
| CLV_C14_Caspase3-7 | 491 | 495 | PF00656 | 0.502 |
| CLV_C14_Caspase3-7 | 612 | 616 | PF00656 | 0.523 |
| CLV_MEL_PAP_1 | 732 | 738 | PF00089 | 0.675 |
| CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.523 |
| CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.463 |
| CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.362 |
| CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.445 |
| CLV_PCSK_FUR_1 | 17 | 21 | PF00082 | 0.634 |
| CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.524 |
| CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.507 |
| CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.282 |
| CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.282 |
| CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.356 |
| CLV_PCSK_KEX2_1 | 661 | 663 | PF00082 | 0.535 |
| CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.502 |
| CLV_PCSK_PC1ET2_1 | 572 | 574 | PF00082 | 0.282 |
| CLV_PCSK_PC1ET2_1 | 613 | 615 | PF00082 | 0.362 |
| CLV_PCSK_PC1ET2_1 | 661 | 663 | PF00082 | 0.560 |
| CLV_PCSK_PC7_1 | 15 | 21 | PF00082 | 0.515 |
| CLV_PCSK_PC7_1 | 568 | 574 | PF00082 | 0.282 |
| CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.367 |
| CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.621 |
| CLV_Separin_Metazoa | 276 | 280 | PF03568 | 0.377 |
| DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.408 |
| DEG_COP1_1 | 63 | 72 | PF00400 | 0.453 |
| DEG_Kelch_Keap1_1 | 375 | 380 | PF01344 | 0.635 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.559 |
| DEG_SPOP_SBC_1 | 373 | 377 | PF00917 | 0.628 |
| DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.650 |
| DOC_MAPK_gen_1 | 572 | 579 | PF00069 | 0.482 |
| DOC_MAPK_MEF2A_6 | 539 | 548 | PF00069 | 0.482 |
| DOC_MAPK_RevD_3 | 655 | 668 | PF00069 | 0.375 |
| DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.522 |
| DOC_PP2B_PxIxI_1 | 311 | 317 | PF00149 | 0.408 |
| DOC_PP4_FxxP_1 | 617 | 620 | PF00568 | 0.496 |
| DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.612 |
| DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.346 |
| DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.496 |
| DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.640 |
| DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.469 |
| DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.511 |
| DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.460 |
| DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.581 |
| DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.517 |
| DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.684 |
| DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.482 |
| DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.552 |
| LIG_14-3-3_CanoR_1 | 17 | 25 | PF00244 | 0.528 |
| LIG_14-3-3_CanoR_1 | 182 | 187 | PF00244 | 0.689 |
| LIG_14-3-3_CanoR_1 | 279 | 289 | PF00244 | 0.471 |
| LIG_14-3-3_CanoR_1 | 331 | 341 | PF00244 | 0.532 |
| LIG_14-3-3_CanoR_1 | 351 | 356 | PF00244 | 0.627 |
| LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.620 |
| LIG_14-3-3_CanoR_1 | 519 | 525 | PF00244 | 0.491 |
| LIG_14-3-3_CanoR_1 | 539 | 548 | PF00244 | 0.452 |
| LIG_14-3-3_CanoR_1 | 692 | 700 | PF00244 | 0.702 |
| LIG_BH_BH3_1 | 36 | 52 | PF00452 | 0.295 |
| LIG_deltaCOP1_diTrp_1 | 380 | 390 | PF00928 | 0.484 |
| LIG_FHA_1 | 252 | 258 | PF00498 | 0.606 |
| LIG_FHA_1 | 320 | 326 | PF00498 | 0.459 |
| LIG_FHA_1 | 491 | 497 | PF00498 | 0.512 |
| LIG_FHA_1 | 558 | 564 | PF00498 | 0.497 |
| LIG_FHA_1 | 87 | 93 | PF00498 | 0.531 |
| LIG_FHA_2 | 263 | 269 | PF00498 | 0.332 |
| LIG_FHA_2 | 333 | 339 | PF00498 | 0.600 |
| LIG_FHA_2 | 630 | 636 | PF00498 | 0.554 |
| LIG_FHA_2 | 676 | 682 | PF00498 | 0.663 |
| LIG_GBD_Chelix_1 | 281 | 289 | PF00786 | 0.411 |
| LIG_LIR_Apic_2 | 615 | 620 | PF02991 | 0.515 |
| LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.511 |
| LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.536 |
| LIG_LIR_Gen_1 | 595 | 603 | PF02991 | 0.482 |
| LIG_LIR_Gen_1 | 650 | 660 | PF02991 | 0.412 |
| LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.426 |
| LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.373 |
| LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.475 |
| LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.529 |
| LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.534 |
| LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.350 |
| LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.482 |
| LIG_LIR_Nem_3 | 650 | 656 | PF02991 | 0.407 |
| LIG_LIR_Nem_3 | 726 | 732 | PF02991 | 0.559 |
| LIG_NRBOX | 562 | 568 | PF00104 | 0.496 |
| LIG_SH2_CRK | 100 | 104 | PF00017 | 0.407 |
| LIG_SH2_PTP2 | 242 | 245 | PF00017 | 0.562 |
| LIG_SH2_PTP2 | 729 | 732 | PF00017 | 0.636 |
| LIG_SH2_SRC | 132 | 135 | PF00017 | 0.567 |
| LIG_SH2_STAP1 | 649 | 653 | PF00017 | 0.427 |
| LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.567 |
| LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.552 |
| LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.482 |
| LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.375 |
| LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.456 |
| LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.490 |
| LIG_SH2_STAT5 | 649 | 652 | PF00017 | 0.498 |
| LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.636 |
| LIG_SH3_3 | 154 | 160 | PF00018 | 0.742 |
| LIG_SH3_3 | 186 | 192 | PF00018 | 0.668 |
| LIG_SH3_3 | 306 | 312 | PF00018 | 0.568 |
| LIG_SH3_3 | 385 | 391 | PF00018 | 0.505 |
| LIG_SH3_3 | 597 | 603 | PF00018 | 0.562 |
| LIG_SH3_3 | 64 | 70 | PF00018 | 0.451 |
| LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.424 |
| LIG_SUMO_SIM_par_1 | 626 | 633 | PF11976 | 0.513 |
| LIG_TYR_ITIM | 98 | 103 | PF00017 | 0.347 |
| MOD_CK1_1 | 233 | 239 | PF00069 | 0.337 |
| MOD_CK1_1 | 375 | 381 | PF00069 | 0.570 |
| MOD_CK1_1 | 395 | 401 | PF00069 | 0.463 |
| MOD_CK1_1 | 53 | 59 | PF00069 | 0.519 |
| MOD_CK1_1 | 605 | 611 | PF00069 | 0.398 |
| MOD_CK1_1 | 703 | 709 | PF00069 | 0.744 |
| MOD_CK2_1 | 331 | 337 | PF00069 | 0.606 |
| MOD_CK2_1 | 374 | 380 | PF00069 | 0.591 |
| MOD_CK2_1 | 620 | 626 | PF00069 | 0.335 |
| MOD_CK2_1 | 666 | 672 | PF00069 | 0.621 |
| MOD_Cter_Amidation | 570 | 573 | PF01082 | 0.335 |
| MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.537 |
| MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.531 |
| MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.561 |
| MOD_GlcNHglycan | 366 | 370 | PF01048 | 0.682 |
| MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.644 |
| MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.565 |
| MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.403 |
| MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.528 |
| MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.412 |
| MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.488 |
| MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.354 |
| MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.460 |
| MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.516 |
| MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.620 |
| MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.605 |
| MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.473 |
| MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.755 |
| MOD_GSK3_1 | 178 | 185 | PF00069 | 0.614 |
| MOD_GSK3_1 | 247 | 254 | PF00069 | 0.424 |
| MOD_GSK3_1 | 332 | 339 | PF00069 | 0.511 |
| MOD_GSK3_1 | 392 | 399 | PF00069 | 0.608 |
| MOD_GSK3_1 | 482 | 489 | PF00069 | 0.587 |
| MOD_GSK3_1 | 630 | 637 | PF00069 | 0.419 |
| MOD_GSK3_1 | 666 | 673 | PF00069 | 0.568 |
| MOD_GSK3_1 | 675 | 682 | PF00069 | 0.668 |
| MOD_LATS_1 | 180 | 186 | PF00433 | 0.621 |
| MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.501 |
| MOD_NEK2_1 | 232 | 237 | PF00069 | 0.340 |
| MOD_NEK2_1 | 247 | 252 | PF00069 | 0.401 |
| MOD_NEK2_1 | 394 | 399 | PF00069 | 0.637 |
| MOD_NEK2_1 | 50 | 55 | PF00069 | 0.444 |
| MOD_NEK2_1 | 547 | 552 | PF00069 | 0.426 |
| MOD_NEK2_1 | 85 | 90 | PF00069 | 0.457 |
| MOD_NEK2_2 | 192 | 197 | PF00069 | 0.316 |
| MOD_PIKK_1 | 557 | 563 | PF00454 | 0.447 |
| MOD_PIKK_1 | 634 | 640 | PF00454 | 0.586 |
| MOD_PIKK_1 | 679 | 685 | PF00454 | 0.719 |
| MOD_PIKK_1 | 714 | 720 | PF00454 | 0.635 |
| MOD_PK_1 | 351 | 357 | PF00069 | 0.632 |
| MOD_PKA_1 | 331 | 337 | PF00069 | 0.447 |
| MOD_PKA_2 | 18 | 24 | PF00069 | 0.682 |
| MOD_PKA_2 | 233 | 239 | PF00069 | 0.320 |
| MOD_PKA_2 | 287 | 293 | PF00069 | 0.558 |
| MOD_PKA_2 | 331 | 337 | PF00069 | 0.649 |
| MOD_PKA_2 | 538 | 544 | PF00069 | 0.342 |
| MOD_PKA_2 | 605 | 611 | PF00069 | 0.371 |
| MOD_PKA_2 | 666 | 672 | PF00069 | 0.588 |
| MOD_PKA_2 | 691 | 697 | PF00069 | 0.693 |
| MOD_PKA_2 | 700 | 706 | PF00069 | 0.604 |
| MOD_Plk_1 | 202 | 208 | PF00069 | 0.335 |
| MOD_Plk_1 | 336 | 342 | PF00069 | 0.618 |
| MOD_Plk_4 | 262 | 268 | PF00069 | 0.433 |
| MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.335 |
| MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.552 |
| MOD_SUMO_rev_2 | 134 | 141 | PF00179 | 0.612 |
| TRG_DiLeu_BaEn_1 | 404 | 409 | PF01217 | 0.406 |
| TRG_DiLeu_BaLyEn_6 | 655 | 660 | PF01217 | 0.385 |
| TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.479 |
| TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.424 |
| TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.435 |
| TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.440 |
| TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.389 |
| TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.636 |
| TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.593 |
| TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.404 |
| TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.367 |
| TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.507 |
| TRG_ER_diArg_1 | 526 | 529 | PF00400 | 0.361 |
| TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.480 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8D8 | Leptomonas seymouri | 53% | 100% |
| A0A1X0P3T2 | Trypanosomatidae | 39% | 100% |
| A0A3S5ISG6 | Trypanosoma rangeli | 38% | 100% |
| A0A3S7X6Z1 | Leishmania donovani | 98% | 100% |
| A4HLV3 | Leishmania braziliensis | 72% | 99% |
| D0A670 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
| E9B480 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
| Q4Q3U6 | Leishmania major | 91% | 99% |
| V5BP75 | Trypanosoma cruzi | 37% | 100% |