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: Q4Q3Q6
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003746 | translation elongation factor activity | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003924 | GTPase activity | 7 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 9 |
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:0045182 | translation regulator activity | 1 | 9 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 9 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 543 | 547 | PF00656 | 0.431 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 824 | 826 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 706 | 708 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.767 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.298 |
CLV_Separin_Metazoa | 767 | 771 | PF03568 | 0.431 |
DEG_SCF_TRCP1_1 | 363 | 368 | PF00400 | 0.431 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.636 |
DOC_ANK_TNKS_1 | 799 | 806 | PF00023 | 0.442 |
DOC_CKS1_1 | 469 | 474 | PF01111 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 534 | 540 | PF00134 | 0.431 |
DOC_CYCLIN_yCln2_LP_2 | 832 | 838 | PF00134 | 0.522 |
DOC_MAPK_gen_1 | 522 | 532 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 577 | 584 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 711 | 717 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 797 | 806 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 525 | 534 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.400 |
DOC_MAPK_NFAT4_5 | 525 | 533 | PF00069 | 0.442 |
DOC_MAPK_RevD_3 | 138 | 154 | PF00069 | 0.370 |
DOC_MAPK_RevD_3 | 606 | 622 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 791 | 797 | PF00149 | 0.535 |
DOC_PP2B_LxvP_1 | 534 | 537 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 564 | 567 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 832 | 835 | PF13499 | 0.518 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 823 | 827 | PF12436 | 0.580 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 493 | 502 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 570 | 575 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 756 | 764 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 481 | 498 | PF00022 | 0.431 |
LIG_Actin_WH2_2 | 757 | 772 | PF00022 | 0.431 |
LIG_APCC_ABBA_1 | 105 | 110 | PF00400 | 0.388 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 637 | 641 | PF00533 | 0.375 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.434 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.598 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.431 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.431 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.601 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.431 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.760 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.362 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.597 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.274 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.313 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.431 |
LIG_FHA_1 | 806 | 812 | PF00498 | 0.431 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.552 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.479 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.388 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.431 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.416 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.563 |
LIG_GBD_Chelix_1 | 166 | 174 | PF00786 | 0.445 |
LIG_GBD_Chelix_1 | 528 | 536 | PF00786 | 0.335 |
LIG_LIR_Gen_1 | 508 | 516 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 669 | 674 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 725 | 729 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 743 | 749 | PF02991 | 0.474 |
LIG_MLH1_MIPbox_1 | 637 | 641 | PF16413 | 0.375 |
LIG_Rb_pABgroove_1 | 480 | 488 | PF01858 | 0.431 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.498 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 486 | 490 | PF00017 | 0.431 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.625 |
LIG_SH2_SRC | 746 | 749 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 763 | 766 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 763 | 766 | PF00017 | 0.456 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.634 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 141 | 147 | PF11976 | 0.540 |
LIG_SUMO_SIM_anti_2 | 732 | 737 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 479 | 487 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 675 | 681 | PF11976 | 0.472 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.424 |
LIG_TRAF2_2 | 48 | 53 | PF00917 | 0.539 |
LIG_TYR_ITIM | 12 | 17 | PF00017 | 0.345 |
LIG_TYR_ITIM | 418 | 423 | PF00017 | 0.411 |
LIG_UBA3_1 | 563 | 571 | PF00899 | 0.303 |
MOD_CDK_SPK_2 | 468 | 473 | PF00069 | 0.309 |
MOD_CDK_SPK_2 | 719 | 724 | PF00069 | 0.377 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.355 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.657 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.703 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.673 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.280 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.266 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.297 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.489 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.687 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.266 |
MOD_CK1_1 | 722 | 728 | PF00069 | 0.432 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.370 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.266 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.359 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.479 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.553 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.741 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.604 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.603 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.326 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.405 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.365 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.351 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.293 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.221 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.266 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.647 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.355 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.270 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.646 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.662 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.495 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.695 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.741 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.298 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.267 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.380 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.254 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.200 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.626 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.404 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.325 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.197 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.266 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.729 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.281 |
MOD_N-GLC_1 | 660 | 665 | PF02516 | 0.425 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.405 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.421 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.265 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.280 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.281 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.433 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.281 |
MOD_NEK2_2 | 463 | 468 | PF00069 | 0.287 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.550 |
MOD_PIKK_1 | 651 | 657 | PF00454 | 0.305 |
MOD_PK_1 | 400 | 406 | PF00069 | 0.266 |
MOD_PKA_1 | 570 | 576 | PF00069 | 0.200 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.560 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.365 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.360 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.266 |
MOD_PKA_2 | 755 | 761 | PF00069 | 0.266 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.564 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.516 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.360 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.331 |
MOD_Plk_1 | 636 | 642 | PF00069 | 0.353 |
MOD_Plk_1 | 660 | 666 | PF00069 | 0.420 |
MOD_Plk_1 | 772 | 778 | PF00069 | 0.266 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.536 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.439 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.602 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.281 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.276 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.242 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.365 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.337 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.341 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.315 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.786 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.774 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.794 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.650 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.403 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.266 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.685 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.489 |
MOD_SUMO_for_1 | 35 | 38 | PF00179 | 0.467 |
MOD_SUMO_for_1 | 702 | 705 | PF00179 | 0.386 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_1 | 790 | 795 | PF01217 | 0.331 |
TRG_DiLeu_BaEn_1 | 813 | 818 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_4 | 4 | 10 | PF01217 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.592 |
TRG_DiLeu_LyEn_5 | 790 | 795 | PF01217 | 0.331 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 746 | 749 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 342 | 345 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.200 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.287 |
TRG_NLS_Bipartite_1 | 153 | 175 | PF00514 | 0.431 |
TRG_NLS_MonoExtC_3 | 824 | 830 | PF00514 | 0.501 |
TRG_NLS_MonoExtN_4 | 823 | 829 | PF00514 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K5 | Leptomonas seymouri | 69% | 100% |
A0A0S4JM58 | Bodo saltans | 53% | 100% |
A0A1X0NRK6 | Trypanosomatidae | 46% | 97% |
A0A3R7MHD3 | Trypanosoma rangeli | 51% | 100% |
A0A3S7X775 | Leishmania donovani | 93% | 100% |
A4HLZ0 | Leishmania braziliensis | 84% | 99% |
A4I9C0 | Leishmania infantum | 93% | 100% |
C9ZJA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9B4B9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BF52 | Trypanosoma cruzi | 50% | 99% |