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:0005634 | nucleus | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AR56
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006397 | mRNA processing | 7 | 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:0016071 | mRNA metabolic process | 6 | 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 |
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 | 10 |
GO:0004518 | nuclease activity | 4 | 7 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0004521 | RNA endonuclease activity | 5 | 7 |
GO:0004540 | RNA nuclease activity | 4 | 7 |
GO:0008419 | RNA lariat debranching enzyme activity | 7 | 7 |
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 | 7 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 7 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 601 | 605 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.341 |
CLV_PCSK_FUR_1 | 363 | 367 | PF00082 | 0.291 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.407 |
CLV_PCSK_PC7_1 | 73 | 79 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.551 |
CLV_Separin_Metazoa | 409 | 413 | PF03568 | 0.391 |
DEG_ODPH_VHL_1 | 458 | 471 | PF01847 | 0.428 |
DEG_SPOP_SBC_1 | 381 | 385 | PF00917 | 0.177 |
DEG_SPOP_SBC_1 | 545 | 549 | PF00917 | 0.630 |
DEG_SPOP_SBC_1 | 582 | 586 | PF00917 | 0.647 |
DOC_MAPK_gen_1 | 348 | 358 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 400 | 410 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 73 | 83 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 92 | 102 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 402 | 410 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.240 |
DOC_PP2B_LxvP_1 | 457 | 460 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.325 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.566 |
DOC_USP7_UBL2_3 | 280 | 284 | PF12436 | 0.356 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 513 | 519 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 536 | 540 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.421 |
LIG_APCC_ABBA_1 | 568 | 573 | PF00400 | 0.645 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.333 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.377 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 413 | 417 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 594 | 598 | PF00533 | 0.596 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.353 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.425 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.385 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.335 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.421 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.394 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.564 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.750 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.605 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.618 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.565 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.341 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.376 |
LIG_FHA_2 | 501 | 507 | PF00498 | 0.713 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.615 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.475 |
LIG_GBD_Chelix_1 | 3 | 11 | PF00786 | 0.572 |
LIG_LIR_Apic_2 | 16 | 22 | PF02991 | 0.587 |
LIG_LIR_Apic_2 | 183 | 189 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 190 | 194 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 340 | 350 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 357 | 364 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 87 | 94 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 87 | 91 | PF02991 | 0.312 |
LIG_Pex14_1 | 44 | 48 | PF04695 | 0.552 |
LIG_Pex14_2 | 279 | 283 | PF04695 | 0.471 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.463 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.399 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.261 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.420 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.399 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.664 |
LIG_SH3_1 | 191 | 197 | PF00018 | 0.386 |
LIG_SH3_2 | 487 | 492 | PF14604 | 0.659 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.727 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.386 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.420 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.454 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.580 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.671 |
LIG_SH3_4 | 280 | 287 | PF00018 | 0.356 |
LIG_SUMO_SIM_par_1 | 168 | 175 | PF11976 | 0.364 |
LIG_UBA3_1 | 7 | 12 | PF00899 | 0.636 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.360 |
LIG_WRPW_2 | 279 | 282 | PF00400 | 0.389 |
LIG_WW_3 | 195 | 199 | PF00397 | 0.493 |
LIG_WW_3 | 607 | 611 | PF00397 | 0.657 |
MOD_CDC14_SPxK_1 | 489 | 492 | PF00782 | 0.617 |
MOD_CDK_SPxK_1 | 486 | 492 | PF00069 | 0.613 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.541 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.457 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.562 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.588 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.365 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.360 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.654 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.674 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.720 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.594 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.518 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.274 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.684 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.666 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.479 |
MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.439 |
MOD_GlcNHglycan | 118 | 122 | PF01048 | 0.531 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.650 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.405 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.397 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.599 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.600 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.614 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.350 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.362 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.577 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.532 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.697 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.784 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.578 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.709 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.521 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.389 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.504 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.603 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.717 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.665 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.493 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.317 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.324 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.705 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.713 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.653 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.464 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.534 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.586 |
MOD_LATS_1 | 527 | 533 | PF00433 | 0.722 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.333 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.617 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.324 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.455 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.209 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.431 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.211 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.581 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.692 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.315 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.398 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.648 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.234 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.398 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.321 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.326 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.489 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.759 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.649 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.604 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.487 |
MOD_PKB_1 | 363 | 371 | PF00069 | 0.326 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.411 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.627 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.378 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.325 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.415 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.210 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.333 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.226 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.409 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.450 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.705 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.532 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.666 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.709 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.677 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.426 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.452 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.627 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.770 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.639 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.566 |
MOD_SUMO_rev_2 | 66 | 75 | PF00179 | 0.271 |
TRG_DiLeu_BaEn_1 | 144 | 149 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 296 | 301 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.210 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.176 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.256 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 400 | 403 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 528 | 531 | PF00400 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYD2 | Leptomonas seymouri | 52% | 100% |
A0A0S4ITU3 | Bodo saltans | 41% | 100% |
A0A3R7KE78 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H711 | Leishmania donovani | 92% | 100% |
A4H947 | Leishmania braziliensis | 82% | 100% |
A4HXG1 | Leishmania infantum | 92% | 100% |
C9ZP39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
Q4QEA7 | Leishmania major | 92% | 99% |