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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4H947
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006397 | mRNA processing | 7 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0016071 | mRNA metabolic process | 6 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 6 |
GO:0004519 | endonuclease activity | 5 | 6 |
GO:0004521 | RNA endonuclease activity | 5 | 6 |
GO:0004540 | RNA nuclease activity | 4 | 6 |
GO:0008419 | RNA lariat debranching enzyme activity | 7 | 6 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 6 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 6 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 6 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.218 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.600 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.386 |
CLV_PCSK_PC7_1 | 493 | 499 | PF00082 | 0.511 |
CLV_PCSK_PC7_1 | 73 | 79 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.249 |
CLV_Separin_Metazoa | 409 | 413 | PF03568 | 0.392 |
DEG_ODPH_VHL_1 | 458 | 471 | PF01847 | 0.470 |
DEG_SCF_FBW7_1 | 241 | 246 | PF00400 | 0.218 |
DEG_SCF_FBW7_1 | 583 | 590 | PF00400 | 0.539 |
DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 534 | 538 | PF00917 | 0.616 |
DEG_SPOP_SBC_1 | 545 | 549 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 582 | 586 | PF00917 | 0.711 |
DEG_SPOP_SBC_1 | 594 | 598 | PF00917 | 0.685 |
DOC_MAPK_gen_1 | 348 | 358 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 400 | 410 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 77 | 83 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 402 | 410 | PF00069 | 0.396 |
DOC_PP2B_LxvP_1 | 457 | 460 | PF13499 | 0.434 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.298 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.526 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.316 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.218 |
LIG_14-3-3_CanoR_1 | 389 | 396 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 492 | 500 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 218 | 234 | PF00022 | 0.218 |
LIG_APCC_ABBA_1 | 568 | 573 | PF00400 | 0.712 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.298 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.386 |
LIG_BRCT_BRCA1_1 | 413 | 417 | PF00533 | 0.386 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.298 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.386 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.263 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.280 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.312 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.386 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.371 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.654 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.661 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.538 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.218 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.344 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.377 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.526 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.392 |
LIG_GBD_Chelix_1 | 3 | 11 | PF00786 | 0.619 |
LIG_LIR_Apic_2 | 183 | 189 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 190 | 194 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 340 | 350 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 357 | 364 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 569 | 576 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 569 | 574 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 87 | 91 | PF02991 | 0.333 |
LIG_LYPXL_SIV_4 | 223 | 231 | PF13949 | 0.218 |
LIG_Pex14_1 | 44 | 48 | PF04695 | 0.513 |
LIG_Pex14_2 | 278 | 282 | PF04695 | 0.392 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.400 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.333 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.333 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.707 |
LIG_SH3_1 | 191 | 197 | PF00018 | 0.304 |
LIG_SH3_2 | 487 | 492 | PF14604 | 0.699 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.304 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.464 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.480 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.605 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.699 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.615 |
LIG_SH3_4 | 279 | 286 | PF00018 | 0.316 |
LIG_SUMO_SIM_par_1 | 168 | 175 | PF11976 | 0.333 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.218 |
LIG_UBA3_1 | 7 | 12 | PF00899 | 0.633 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 443 | 448 | PF05994 | 0.325 |
LIG_WRPW_2 | 278 | 281 | PF00400 | 0.298 |
LIG_WW_3 | 195 | 199 | PF00397 | 0.392 |
LIG_WW_3 | 607 | 611 | PF00397 | 0.710 |
MOD_CDK_SPxK_1 | 604 | 610 | PF00069 | 0.549 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.365 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.633 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.386 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.360 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.317 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.536 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.236 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.530 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.741 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.588 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.727 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.660 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.377 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.552 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.550 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.500 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.720 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.677 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.400 |
MOD_Cter_Amidation | 495 | 498 | PF01082 | 0.514 |
MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.333 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.405 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.713 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.414 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.333 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.690 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.609 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.622 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.324 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.539 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.521 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.797 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.598 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.723 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.392 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.563 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.400 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.462 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.674 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.519 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.300 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.680 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.599 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.731 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.662 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.491 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.604 |
MOD_LATS_1 | 527 | 533 | PF00433 | 0.714 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.333 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.536 |
MOD_N-GLC_2 | 66 | 68 | PF02516 | 0.218 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.333 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.418 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.338 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.433 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.230 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.578 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.639 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.298 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.386 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.694 |
MOD_PIKK_1 | 621 | 627 | PF00454 | 0.615 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.218 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.386 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.298 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.358 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.513 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.523 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.671 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.392 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.218 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.218 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.391 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.333 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.538 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.298 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.386 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.392 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.364 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.756 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.677 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.710 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.338 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.519 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.645 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.473 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.611 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.681 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.592 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.589 |
TRG_DiLeu_BaEn_1 | 144 | 149 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 295 | 300 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.183 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.162 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 400 | 403 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 528 | 531 | PF00400 | 0.710 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYD2 | Leptomonas seymouri | 51% | 100% |
A0A3R7KE78 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H711 | Leishmania donovani | 81% | 100% |
A4HXG1 | Leishmania infantum | 81% | 100% |
C9ZP39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AR56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QEA7 | Leishmania major | 82% | 98% |