Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
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: 6 |
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:0018444 | translation release factor complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ANQ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 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:0019538 | protein metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003924 | GTPase activity | 7 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005525 | GTP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019001 | guanyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003747 | translation release factor activity | 5 | 1 |
GO:0008079 | translation termination factor activity | 4 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 2 |
GO:0045182 | translation regulator activity | 1 | 2 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 2 |
GO:0003746 | translation elongation factor activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.748 |
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.299 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.248 |
CLV_PCSK_PC1ET2_1 | 324 | 326 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.244 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.693 |
DOC_ANK_TNKS_1 | 743 | 750 | PF00023 | 0.551 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.596 |
DOC_CKS1_1 | 249 | 254 | PF01111 | 0.682 |
DOC_CYCLIN_yCln2_LP_2 | 719 | 725 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 204 | 213 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 324 | 335 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 508 | 517 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 538 | 545 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 744 | 752 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 508 | 515 | PF00149 | 0.461 |
DOC_PP1_RVXF_1 | 646 | 653 | PF00149 | 0.373 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.447 |
DOC_PP2B_LxvP_1 | 549 | 552 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 561 | 564 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.447 |
DOC_USP7_MATH_2 | 226 | 232 | PF00917 | 0.697 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.654 |
DOC_USP7_UBL2_3 | 320 | 324 | PF12436 | 0.637 |
DOC_USP7_UBL2_3 | 570 | 574 | PF12436 | 0.489 |
DOC_USP7_UBL2_3 | 687 | 691 | PF12436 | 0.438 |
DOC_USP7_UBL2_3 | 729 | 733 | PF12436 | 0.447 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.477 |
LIG_APCC_ABBA_1 | 725 | 730 | PF00400 | 0.499 |
LIG_APCC_ABBAyCdc20_2 | 80 | 86 | PF00400 | 0.689 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.608 |
LIG_BIR_III_4 | 414 | 418 | PF00653 | 0.447 |
LIG_BRCT_BRCA1_1 | 609 | 613 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_2 | 609 | 615 | PF00533 | 0.501 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.653 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.447 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.688 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.447 |
LIG_FHA_1 | 743 | 749 | PF00498 | 0.447 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.734 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.798 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.779 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.637 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.531 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.447 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.314 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.447 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.472 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.426 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.433 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.355 |
LIG_FXI_DFP_1 | 728 | 732 | PF00024 | 0.261 |
LIG_IRF3_LxIS_1 | 434 | 440 | PF10401 | 0.447 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.619 |
LIG_LIR_Apic_2 | 47 | 51 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 558 | 564 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 378 | 385 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 486 | 495 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 682 | 692 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 730 | 739 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 378 | 382 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 730 | 734 | PF02991 | 0.481 |
LIG_PCNA_APIM_2 | 734 | 740 | PF02747 | 0.447 |
LIG_Pex14_1 | 377 | 381 | PF04695 | 0.447 |
LIG_Pex14_2 | 331 | 335 | PF04695 | 0.461 |
LIG_Pex14_2 | 446 | 450 | PF04695 | 0.447 |
LIG_REV1ctd_RIR_1 | 650 | 660 | PF16727 | 0.499 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.783 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.447 |
LIG_SH2_GRB2like | 24 | 27 | PF00017 | 0.668 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.664 |
LIG_SH2_SRC | 379 | 382 | PF00017 | 0.447 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.721 |
LIG_SH2_STAP1 | 379 | 383 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 121 | 124 | PF00017 | 0.709 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.434 |
LIG_SH2_STAT3 | 28 | 31 | PF00017 | 0.667 |
LIG_SH2_STAT3 | 49 | 52 | PF00017 | 0.660 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.358 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.628 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.737 |
LIG_SH3_3 | 721 | 727 | PF00018 | 0.499 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.610 |
LIG_SUMO_SIM_par_1 | 435 | 441 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 656 | 661 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 720 | 726 | PF11976 | 0.527 |
LIG_SxIP_EBH_1 | 636 | 648 | PF03271 | 0.417 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.736 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.683 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.557 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.478 |
LIG_TRAF2_1 | 678 | 681 | PF00917 | 0.447 |
LIG_UBA3_1 | 471 | 477 | PF00899 | 0.461 |
LIG_UBA3_1 | 542 | 550 | PF00899 | 0.551 |
LIG_UBA3_1 | 688 | 695 | PF00899 | 0.493 |
MOD_CDK_SPxxK_3 | 297 | 304 | PF00069 | 0.695 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.770 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.447 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.461 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.489 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.395 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.501 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.731 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.661 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.719 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.559 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.447 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.446 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.449 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.375 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.399 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.391 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.551 |
MOD_CK2_1 | 754 | 760 | PF00069 | 0.452 |
MOD_Cter_Amidation | 213 | 216 | PF01082 | 0.673 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.766 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.726 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.687 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.736 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.662 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.247 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.360 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.327 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.351 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.691 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.781 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.683 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.478 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.400 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.388 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.459 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.659 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.643 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.447 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.447 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.470 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.439 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.704 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.788 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.447 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.735 |
MOD_PKA_1 | 408 | 414 | PF00069 | 0.447 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.451 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.406 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.499 |
MOD_PKB_1 | 314 | 322 | PF00069 | 0.685 |
MOD_Plk_1 | 681 | 687 | PF00069 | 0.461 |
MOD_Plk_2-3 | 553 | 559 | PF00069 | 0.452 |
MOD_Plk_2-3 | 604 | 610 | PF00069 | 0.396 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.443 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.415 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.462 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.711 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.702 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.730 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.749 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.769 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.599 |
MOD_SUMO_for_1 | 308 | 311 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 234 | 243 | PF00179 | 0.749 |
MOD_SUMO_rev_2 | 479 | 484 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 544 | 552 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 571 | 575 | PF00179 | 0.488 |
TRG_DiLeu_BaEn_1 | 458 | 463 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.340 |
TRG_NLS_Bipartite_1 | 204 | 219 | PF00514 | 0.750 |
TRG_NLS_MonoExtN_4 | 203 | 208 | PF00514 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 627 | 631 | PF00026 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAZ5 | Leptomonas seymouri | 78% | 100% |
A0A0S4IX91 | Bodo saltans | 62% | 100% |
A0A1X0NV54 | Trypanosomatidae | 71% | 100% |
A0A3Q8ICH2 | Leishmania donovani | 93% | 100% |
A0A3R7MLL0 | Trypanosoma rangeli | 71% | 100% |
A0A3S7X9T0 | Leishmania donovani | 32% | 100% |
A4H6P3 | Leishmania braziliensis | 88% | 100% |
A4HN87 | Leishmania braziliensis | 32% | 100% |
A4HV24 | Leishmania infantum | 92% | 100% |
A4IBV5 | Leishmania infantum | 31% | 100% |
C9ZYQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A7C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9AFP2 | Leishmania major | 31% | 100% |
E9B6U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O13354 | Candida albicans | 41% | 100% |
O74718 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
P23637 | Ogataea pini | 40% | 100% |
Q2KHZ2 | Bos taurus | 35% | 100% |
Q4QGW5 | Leishmania major | 97% | 100% |
Q9HGI7 | Candida maltosa | 39% | 100% |
Q9HGI8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 38% | 100% |