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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9B4B9
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 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:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003924 | GTPase activity | 7 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003746 | translation elongation factor activity | 4 | 8 |
GO:0008135 | translation factor activity, RNA binding | 3 | 8 |
GO:0045182 | translation regulator activity | 1 | 8 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 538 | 542 | PF00656 | 0.437 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 788 | 792 | PF00082 | 0.306 |
CLV_Separin_Metazoa | 762 | 766 | PF03568 | 0.437 |
DEG_SCF_FBW7_2 | 589 | 594 | PF00400 | 0.388 |
DEG_SCF_TRCP1_1 | 358 | 363 | PF00400 | 0.437 |
DEG_SPOP_SBC_1 | 321 | 325 | PF00917 | 0.655 |
DOC_ANK_TNKS_1 | 794 | 801 | PF00023 | 0.448 |
DOC_CYCLIN_yCln2_LP_2 | 529 | 535 | PF00134 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 827 | 833 | PF00134 | 0.543 |
DOC_MAPK_gen_1 | 517 | 527 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 572 | 579 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 706 | 712 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 792 | 801 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 520 | 529 | PF00069 | 0.437 |
DOC_MAPK_NFAT4_5 | 520 | 528 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 138 | 154 | PF00069 | 0.364 |
DOC_MAPK_RevD_3 | 601 | 617 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 786 | 792 | PF00149 | 0.555 |
DOC_PP2B_LxvP_1 | 529 | 532 | PF13499 | 0.460 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 827 | 830 | PF13499 | 0.535 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.414 |
DOC_USP7_UBL2_3 | 818 | 822 | PF12436 | 0.583 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 714 | 719 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 310 | 318 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 463 | 470 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 488 | 497 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 620 | 626 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 751 | 759 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 476 | 493 | PF00022 | 0.437 |
LIG_Actin_WH2_2 | 752 | 767 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 105 | 110 | PF00400 | 0.398 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.537 |
LIG_BIR_III_2 | 541 | 545 | PF00653 | 0.523 |
LIG_BRCT_BRCA1_1 | 632 | 636 | PF00533 | 0.382 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.447 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.626 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.438 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.450 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.578 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.413 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.437 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.372 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.634 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.361 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.379 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.437 |
LIG_FHA_1 | 801 | 807 | PF00498 | 0.437 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.556 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.485 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.392 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.437 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.435 |
LIG_GBD_Chelix_1 | 166 | 174 | PF00786 | 0.451 |
LIG_GBD_Chelix_1 | 523 | 531 | PF00786 | 0.339 |
LIG_LIR_Gen_1 | 503 | 511 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 503 | 507 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 664 | 669 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 720 | 724 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 738 | 744 | PF02991 | 0.562 |
LIG_MLH1_MIPbox_1 | 632 | 636 | PF16413 | 0.382 |
LIG_Rb_pABgroove_1 | 475 | 483 | PF01858 | 0.437 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.504 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.593 |
LIG_SH2_NCK_1 | 481 | 485 | PF00017 | 0.437 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.636 |
LIG_SH2_SRC | 741 | 744 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 504 | 508 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.382 |
LIG_SH2_STAT3 | 758 | 761 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 758 | 761 | PF00017 | 0.462 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.608 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.657 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.539 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 141 | 147 | PF11976 | 0.539 |
LIG_SUMO_SIM_anti_2 | 727 | 732 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 474 | 482 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 670 | 676 | PF11976 | 0.477 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.415 |
LIG_TYR_ITIM | 413 | 418 | PF00017 | 0.417 |
LIG_UBA3_1 | 558 | 566 | PF00899 | 0.312 |
MOD_CDK_SPK_2 | 714 | 719 | PF00069 | 0.386 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.709 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.748 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.688 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.298 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.325 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.294 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.460 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.696 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.296 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.437 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.431 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.274 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.384 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.481 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.587 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.564 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.309 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.428 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.393 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.379 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.232 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.286 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.684 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.361 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.321 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.471 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.313 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.750 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.536 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.792 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.324 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.277 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.367 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.291 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.677 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.410 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.391 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.303 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.286 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.735 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.704 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.289 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.432 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.401 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.420 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.279 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.306 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.309 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.473 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.562 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.297 |
MOD_NEK2_2 | 458 | 463 | PF00069 | 0.302 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.589 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.334 |
MOD_PK_1 | 395 | 401 | PF00069 | 0.274 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.534 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.548 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.326 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.374 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.274 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.274 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.566 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.529 |
MOD_Plk_1 | 548 | 554 | PF00069 | 0.368 |
MOD_Plk_1 | 575 | 581 | PF00069 | 0.350 |
MOD_Plk_1 | 631 | 637 | PF00069 | 0.360 |
MOD_Plk_1 | 655 | 661 | PF00069 | 0.427 |
MOD_Plk_1 | 767 | 773 | PF00069 | 0.294 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.526 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.519 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.499 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.621 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.289 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.289 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.251 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.400 |
MOD_Plk_4 | 639 | 645 | PF00069 | 0.344 |
MOD_Plk_4 | 655 | 661 | PF00069 | 0.424 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.324 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.674 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.773 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.802 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.660 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.484 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.274 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.205 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.740 |
MOD_ProDKin_1 | 714 | 720 | PF00069 | 0.493 |
MOD_SUMO_for_1 | 35 | 38 | PF00179 | 0.449 |
MOD_SUMO_for_1 | 697 | 700 | PF00179 | 0.393 |
TRG_DiLeu_BaEn_1 | 247 | 252 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 785 | 790 | PF01217 | 0.350 |
TRG_DiLeu_BaEn_1 | 808 | 813 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 554 | 559 | PF01217 | 0.169 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.548 |
TRG_DiLeu_LyEn_5 | 785 | 790 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 571 | 573 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.407 |
TRG_NLS_Bipartite_1 | 153 | 175 | PF00514 | 0.434 |
TRG_NLS_MonoExtC_3 | 819 | 825 | PF00514 | 0.503 |
TRG_NLS_MonoExtN_4 | 818 | 824 | PF00514 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K5 | Leptomonas seymouri | 69% | 100% |
A0A0S4JM58 | Bodo saltans | 52% | 100% |
A0A1X0NRK6 | Trypanosomatidae | 46% | 96% |
A0A3R7MHD3 | Trypanosoma rangeli | 50% | 100% |
A0A3S7X775 | Leishmania donovani | 93% | 99% |
A4HLZ0 | Leishmania braziliensis | 83% | 100% |
A4I9C0 | Leishmania infantum | 93% | 99% |
C9ZJA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
Q4Q3Q6 | Leishmania major | 91% | 100% |
V5BF52 | Trypanosoma cruzi | 50% | 98% |