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: A4HLV3
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 | 249 | 253 | PF00656 | 0.421 |
CLV_C14_Caspase3-7 | 25 | 29 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 496 | 500 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 628 | 632 | PF00656 | 0.406 |
CLV_MEL_PAP_1 | 725 | 731 | PF00089 | 0.670 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.362 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.356 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 565 | 567 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 606 | 608 | PF00082 | 0.362 |
CLV_PCSK_PC7_1 | 561 | 567 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.530 |
CLV_Separin_Metazoa | 269 | 273 | PF03568 | 0.374 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.578 |
DEG_SPOP_SBC_1 | 386 | 390 | PF00917 | 0.645 |
DEG_SPOP_SBC_1 | 623 | 627 | PF00917 | 0.562 |
DOC_MAPK_gen_1 | 565 | 572 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 532 | 541 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 321 | 327 | PF00149 | 0.316 |
DOC_PP1_RVXF_1 | 44 | 51 | PF00149 | 0.364 |
DOC_PP4_FxxP_1 | 610 | 613 | PF00568 | 0.496 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.722 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 729 | 734 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 756 | 761 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 150 | 157 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 173 | 182 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 272 | 282 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 385 | 395 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 424 | 434 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 532 | 541 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 678 | 682 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 685 | 693 | PF00244 | 0.667 |
LIG_deltaCOP1_diTrp_1 | 337 | 341 | PF00928 | 0.292 |
LIG_deltaCOP1_diTrp_1 | 372 | 383 | PF00928 | 0.473 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.427 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.470 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.307 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.497 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.615 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.579 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.417 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.361 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.473 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.631 |
LIG_Integrin_RGD_1 | 26 | 28 | PF01839 | 0.538 |
LIG_LIR_Apic_2 | 608 | 613 | PF02991 | 0.515 |
LIG_LIR_Apic_2 | 63 | 68 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 398 | 408 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 420 | 430 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 588 | 597 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 643 | 653 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 98 | 108 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 420 | 425 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 547 | 552 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 567 | 571 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 719 | 725 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.350 |
LIG_PCNA_PIPBox_1 | 711 | 720 | PF02747 | 0.613 |
LIG_PCNA_yPIPBox_3 | 711 | 720 | PF02747 | 0.565 |
LIG_PTB_Apo_2 | 376 | 383 | PF02174 | 0.272 |
LIG_PTB_Phospho_1 | 376 | 382 | PF10480 | 0.274 |
LIG_Rb_pABgroove_1 | 712 | 720 | PF01858 | 0.512 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.438 |
LIG_SH2_CRK | 597 | 601 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 597 | 601 | PF00017 | 0.408 |
LIG_SH2_PTP2 | 235 | 238 | PF00017 | 0.562 |
LIG_SH2_PTP2 | 722 | 725 | PF00017 | 0.626 |
LIG_SH2_SRC | 132 | 135 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 718 | 722 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.626 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.785 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.466 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.563 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.490 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.562 |
LIG_SH3_3 | 757 | 763 | PF00018 | 0.545 |
LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 263 | 269 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 619 | 629 | PF11976 | 0.513 |
LIG_TRAF2_1 | 680 | 683 | PF00917 | 0.619 |
MOD_CDK_SPxxK_3 | 95 | 102 | PF00069 | 0.518 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.635 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.337 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.300 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.478 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.630 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.541 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.398 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.547 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.529 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.534 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.535 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.374 |
MOD_CK2_1 | 613 | 619 | PF00069 | 0.335 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.467 |
MOD_Cter_Amidation | 563 | 566 | PF01082 | 0.335 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.557 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.648 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.438 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.546 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.527 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.556 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.321 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.657 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.396 |
MOD_GlcNHglycan | 438 | 442 | PF01048 | 0.510 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.417 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.507 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.354 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.587 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.573 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.779 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.620 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.511 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.648 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.601 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.373 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.411 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.581 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.428 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.341 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.659 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.510 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.340 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.354 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.423 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.448 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.460 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.426 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.691 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.447 |
MOD_PIKK_1 | 707 | 713 | PF00454 | 0.613 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.530 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.700 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.320 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.535 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.399 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.393 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.342 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.371 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.613 |
MOD_PKB_1 | 17 | 25 | PF00069 | 0.633 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.335 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.413 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.289 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.309 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.642 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.512 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.456 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.335 |
MOD_ProDKin_1 | 729 | 735 | PF00069 | 0.553 |
MOD_ProDKin_1 | 756 | 762 | PF00069 | 0.535 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.496 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 134 | 140 | PF00179 | 0.648 |
MOD_SUMO_rev_2 | 248 | 256 | PF00179 | 0.402 |
TRG_DiLeu_BaEn_1 | 398 | 403 | PF01217 | 0.406 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.299 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.626 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 316 | 320 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8D8 | Leptomonas seymouri | 52% | 99% |
A0A1X0P3T2 | Trypanosomatidae | 38% | 100% |
A0A3S5ISG6 | Trypanosoma rangeli | 37% | 100% |
A0A3S7X6Z1 | Leishmania donovani | 73% | 100% |
D0A670 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AHQ9 | Leishmania infantum | 72% | 99% |
E9B480 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q3U6 | Leishmania major | 73% | 100% |
V5BP75 | Trypanosoma cruzi | 36% | 100% |