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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ASL2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004519 | endonuclease activity | 5 | 10 |
GO:0004521 | RNA endonuclease activity | 5 | 10 |
GO:0004525 | ribonuclease III activity | 6 | 10 |
GO:0004540 | RNA nuclease activity | 4 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 10 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 10 |
GO:0032296 | double-stranded RNA-specific ribonuclease activity | 5 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0004129 | cytochrome-c oxidase activity | 4 | 1 |
GO:0005215 | transporter activity | 1 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0009055 | electron transfer activity | 3 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015078 | proton transmembrane transporter activity | 5 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 1 |
GO:0015453 | oxidoreduction-driven active transmembrane transporter activity | 5 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 2 |
GO:0016675 | oxidoreductase activity, acting on a heme group of donors | 3 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.742 |
CLV_PCSK_FUR_1 | 199 | 203 | PF00082 | 0.288 |
CLV_PCSK_FUR_1 | 403 | 407 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 109 | 111 | PF00082 | 0.791 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.805 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.480 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.444 |
DEG_APCC_DBOX_1 | 547 | 555 | PF00400 | 0.707 |
DEG_SPOP_SBC_1 | 570 | 574 | PF00917 | 0.803 |
DOC_CDC14_PxL_1 | 420 | 428 | PF14671 | 0.611 |
DOC_CYCLIN_yCln2_LP_2 | 422 | 425 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 156 | 166 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 181 | 187 | PF00069 | 0.692 |
DOC_MAPK_gen_1 | 201 | 211 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 431 | 438 | PF00069 | 0.691 |
DOC_MAPK_gen_1 | 439 | 445 | PF00069 | 0.630 |
DOC_MAPK_gen_1 | 76 | 83 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 159 | 168 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 431 | 438 | PF00069 | 0.684 |
DOC_MAPK_MEF2A_6 | 76 | 85 | PF00069 | 0.568 |
DOC_PP1_RVXF_1 | 325 | 332 | PF00149 | 0.502 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.457 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 17 | 27 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 189 | 194 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 263 | 268 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 348 | 354 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 563 | 567 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 571 | 578 | PF00244 | 0.676 |
LIG_Actin_WH2_2 | 371 | 389 | PF00022 | 0.527 |
LIG_Actin_WH2_2 | 62 | 78 | PF00022 | 0.351 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.783 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.613 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.686 |
LIG_eIF4E_1 | 134 | 140 | PF01652 | 0.623 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.454 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.609 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.517 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.758 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.604 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.602 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.450 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.584 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.599 |
LIG_HP1_1 | 70 | 74 | PF01393 | 0.540 |
LIG_LIR_Apic_2 | 340 | 345 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 160 | 168 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 184 | 193 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 243 | 251 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 340 | 344 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.376 |
LIG_MAD2 | 25 | 33 | PF02301 | 0.655 |
LIG_NRBOX | 325 | 331 | PF00104 | 0.494 |
LIG_Pex14_1 | 203 | 207 | PF04695 | 0.434 |
LIG_Pex14_1 | 337 | 341 | PF04695 | 0.674 |
LIG_REV1ctd_RIR_1 | 252 | 260 | PF16727 | 0.531 |
LIG_RPA_C_Fungi | 197 | 209 | PF08784 | 0.561 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.641 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.500 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.688 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.608 |
LIG_SH2_NCK_1 | 342 | 346 | PF00017 | 0.688 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.675 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 59 | 63 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.619 |
LIG_SH3_2 | 458 | 463 | PF14604 | 0.777 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.685 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.683 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.746 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.714 |
LIG_SUMO_SIM_anti_2 | 162 | 168 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 188 | 197 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 291 | 297 | PF11976 | 0.450 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.543 |
LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.721 |
LIG_TRFH_1 | 420 | 424 | PF08558 | 0.519 |
LIG_UBA3_1 | 208 | 213 | PF00899 | 0.535 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.554 |
LIG_WW_3 | 178 | 182 | PF00397 | 0.606 |
MOD_CDK_SPxK_1 | 257 | 263 | PF00069 | 0.556 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.616 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.712 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.470 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.536 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.780 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.694 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.757 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.547 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.706 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.678 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.614 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.492 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.613 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.441 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.522 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.574 |
MOD_DYRK1A_RPxSP_1 | 563 | 567 | PF00069 | 0.471 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.627 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.495 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.478 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.665 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.709 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.750 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.455 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.704 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.560 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.618 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.679 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.565 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.522 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.500 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.726 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.537 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.471 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.498 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.498 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.459 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.589 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.650 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.504 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.632 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.221 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.492 |
MOD_NEK2_2 | 434 | 439 | PF00069 | 0.580 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.331 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.653 |
MOD_PKA_1 | 181 | 187 | PF00069 | 0.692 |
MOD_PKA_1 | 485 | 491 | PF00069 | 0.617 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.692 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.592 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.728 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.751 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.723 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.465 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.514 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.504 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.673 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.514 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.758 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.561 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.556 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.678 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.762 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.678 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.681 |
MOD_SUMO_rev_2 | 104 | 111 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 320 | 329 | PF00179 | 0.518 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_2 | 106 | 112 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.634 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.572 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.611 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.739 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.745 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.357 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7V7 | Leptomonas seymouri | 40% | 92% |
A0A1X0P8F1 | Trypanosomatidae | 36% | 90% |
A0A3S7XAF0 | Leishmania donovani | 87% | 100% |
A0A422MWV0 | Trypanosoma rangeli | 35% | 98% |
A4ICP2 | Leishmania infantum | 87% | 100% |
E9AIX5 | Leishmania braziliensis | 75% | 100% |
Q4Q1Y4 | Leishmania major | 86% | 100% |
V5BZV5 | Trypanosoma cruzi | 35% | 98% |