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: A4HLZ0
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 | 554 | 558 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 721 | 723 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 836 | 838 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 717 | 719 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 836 | 838 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 717 | 719 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 837 | 841 | PF00082 | 0.531 |
CLV_Separin_Metazoa | 778 | 782 | PF03568 | 0.437 |
DEG_SCF_FBW7_1 | 216 | 223 | PF00400 | 0.524 |
DEG_SCF_TRCP1_1 | 371 | 376 | PF00400 | 0.437 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 333 | 337 | PF00917 | 0.797 |
DEG_SPOP_SBC_1 | 761 | 765 | PF00917 | 0.379 |
DOC_ANK_TNKS_1 | 810 | 817 | PF00023 | 0.448 |
DOC_CKS1_1 | 480 | 485 | PF01111 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 545 | 551 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 533 | 543 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 588 | 595 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 722 | 728 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 808 | 817 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 536 | 545 | PF00069 | 0.437 |
DOC_MAPK_NFAT4_5 | 536 | 544 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 617 | 633 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 802 | 808 | PF00149 | 0.555 |
DOC_PP2B_LxvP_1 | 301 | 304 | PF13499 | 0.517 |
DOC_PP2B_LxvP_1 | 545 | 548 | PF13499 | 0.460 |
DOC_PP2B_LxvP_1 | 575 | 578 | PF13499 | 0.437 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 843 | 847 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 834 | 838 | PF12436 | 0.585 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 504 | 513 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 636 | 642 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 767 | 775 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 492 | 509 | PF00022 | 0.437 |
LIG_Actin_WH2_2 | 768 | 783 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 110 | 115 | PF00400 | 0.390 |
LIG_BIR_III_2 | 557 | 561 | PF00653 | 0.523 |
LIG_BRCT_BRCA1_1 | 648 | 652 | PF00533 | 0.383 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.368 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.469 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.628 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.438 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.450 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.615 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.437 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.374 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.364 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.379 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.636 |
LIG_FHA_1 | 810 | 816 | PF00498 | 0.437 |
LIG_FHA_1 | 817 | 823 | PF00498 | 0.437 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.485 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.587 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.392 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.437 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.645 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.437 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.486 |
LIG_GBD_Chelix_1 | 171 | 179 | PF00786 | 0.452 |
LIG_GBD_Chelix_1 | 5 | 13 | PF00786 | 0.323 |
LIG_GBD_Chelix_1 | 539 | 547 | PF00786 | 0.339 |
LIG_LIR_Gen_1 | 375 | 381 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 519 | 527 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 519 | 523 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 680 | 685 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 736 | 740 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 754 | 760 | PF02991 | 0.562 |
LIG_MLH1_MIPbox_1 | 648 | 652 | PF16413 | 0.383 |
LIG_PCNA_yPIPBox_3 | 95 | 109 | PF02747 | 0.425 |
LIG_Rb_pABgroove_1 | 491 | 499 | PF01858 | 0.437 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.504 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 497 | 501 | PF00017 | 0.437 |
LIG_SH2_SRC | 757 | 760 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 774 | 777 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 798 | 801 | PF00017 | 0.458 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.640 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.539 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 146 | 152 | PF11976 | 0.552 |
LIG_SUMO_SIM_anti_2 | 743 | 748 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 490 | 498 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 686 | 692 | PF11976 | 0.479 |
LIG_TYR_ITIM | 426 | 431 | PF00017 | 0.417 |
LIG_UBA3_1 | 574 | 582 | PF00899 | 0.312 |
MOD_CDK_SPK_2 | 479 | 484 | PF00069 | 0.326 |
MOD_CDK_SPK_2 | 730 | 735 | PF00069 | 0.381 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.718 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.729 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.567 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.728 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.298 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.325 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.294 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.347 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.296 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.693 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.437 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.274 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.481 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.606 |
MOD_CK2_1 | 698 | 704 | PF00069 | 0.291 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.445 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.609 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.533 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.636 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.628 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.309 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.428 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.379 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.232 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.286 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.694 |
MOD_GlcNHglycan | 699 | 703 | PF01048 | 0.517 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.362 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.321 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.740 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.747 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.673 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.526 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.644 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.719 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.324 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.277 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.429 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.345 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.291 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.640 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.412 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.391 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.303 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.286 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.288 |
MOD_N-GLC_1 | 612 | 617 | PF02516 | 0.289 |
MOD_N-GLC_1 | 671 | 676 | PF02516 | 0.433 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.404 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.419 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.640 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.279 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.306 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.309 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.476 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.297 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.337 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.593 |
MOD_PK_1 | 408 | 414 | PF00069 | 0.274 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.538 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.326 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.374 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.274 |
MOD_PKA_2 | 766 | 772 | PF00069 | 0.274 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.535 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.323 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.368 |
MOD_Plk_1 | 591 | 597 | PF00069 | 0.350 |
MOD_Plk_1 | 647 | 653 | PF00069 | 0.360 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.428 |
MOD_Plk_1 | 783 | 789 | PF00069 | 0.294 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.525 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.556 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.544 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.514 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.599 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.289 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.360 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.289 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.251 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.400 |
MOD_Plk_4 | 655 | 661 | PF00069 | 0.347 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.425 |
MOD_Plk_4 | 733 | 739 | PF00069 | 0.324 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.371 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.670 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.611 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.786 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.655 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.427 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.274 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.712 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 713 | 716 | PF00179 | 0.395 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.451 |
TRG_DiLeu_BaEn_1 | 801 | 806 | PF01217 | 0.350 |
TRG_DiLeu_BaEn_1 | 824 | 829 | PF01217 | 0.478 |
TRG_DiLeu_LyEn_5 | 801 | 806 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 757 | 760 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 587 | 589 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 835 | 837 | PF00400 | 0.436 |
TRG_NLS_Bipartite_1 | 158 | 180 | PF00514 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 588 | 592 | PF00026 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K5 | Leptomonas seymouri | 69% | 100% |
A0A0S4JM58 | Bodo saltans | 52% | 100% |
A0A1X0NRK6 | Trypanosomatidae | 48% | 98% |
A0A3R7MHD3 | Trypanosoma rangeli | 53% | 100% |
A0A3S7X775 | Leishmania donovani | 84% | 100% |
A4I9C0 | Leishmania infantum | 84% | 100% |
C9ZJA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9B4B9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q3Q6 | Leishmania major | 84% | 99% |
V5BF52 | Trypanosoma cruzi | 50% | 100% |