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 | 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: A4HXG1
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:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
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: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 | 591 | 595 | PF00656 | 0.688 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.737 |
CLV_PCSK_FUR_1 | 363 | 367 | PF00082 | 0.368 |
CLV_PCSK_FUR_1 | 390 | 394 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.522 |
CLV_PCSK_PC7_1 | 73 | 79 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.552 |
CLV_Separin_Metazoa | 399 | 403 | PF03568 | 0.409 |
DEG_ODPH_VHL_1 | 448 | 461 | PF01847 | 0.545 |
DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.683 |
DEG_SPOP_SBC_1 | 535 | 539 | PF00917 | 0.694 |
DEG_SPOP_SBC_1 | 572 | 576 | PF00917 | 0.716 |
DOC_CYCLIN_yCln2_LP_2 | 292 | 298 | PF00134 | 0.395 |
DOC_MAPK_gen_1 | 348 | 358 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 390 | 400 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 77 | 83 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 92 | 102 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 392 | 400 | PF00069 | 0.382 |
DOC_PP2B_LxvP_1 | 447 | 450 | PF13499 | 0.469 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.359 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.538 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.658 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.709 |
DOC_USP7_UBL2_3 | 280 | 284 | PF12436 | 0.425 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 402 | 408 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 503 | 509 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 526 | 531 | PF00244 | 0.731 |
LIG_APCC_ABBA_1 | 558 | 563 | PF00400 | 0.764 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.555 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.384 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.368 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 403 | 407 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 584 | 588 | PF00533 | 0.720 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.340 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.525 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.340 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.320 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.397 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.390 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.569 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.731 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.707 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.399 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.715 |
LIG_FHA_2 | 589 | 595 | PF00498 | 0.709 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.481 |
LIG_GBD_Chelix_1 | 3 | 11 | PF00786 | 0.677 |
LIG_IBAR_NPY_1 | 294 | 296 | PF08397 | 0.410 |
LIG_LIR_Apic_2 | 16 | 22 | PF02991 | 0.652 |
LIG_LIR_Apic_2 | 183 | 189 | PF02991 | 0.407 |
LIG_LIR_Apic_2 | 190 | 194 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 340 | 350 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 357 | 364 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 394 | 403 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 87 | 94 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 87 | 91 | PF02991 | 0.351 |
LIG_Pex14_1 | 44 | 48 | PF04695 | 0.521 |
LIG_Pex14_2 | 279 | 283 | PF04695 | 0.488 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.483 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.432 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.432 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.766 |
LIG_SH3_1 | 191 | 197 | PF00018 | 0.400 |
LIG_SH3_2 | 477 | 482 | PF14604 | 0.768 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.718 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.398 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.533 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.459 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.593 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.723 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.620 |
LIG_SH3_4 | 280 | 287 | PF00018 | 0.420 |
LIG_SUMO_SIM_par_1 | 168 | 174 | PF11976 | 0.389 |
LIG_UBA3_1 | 7 | 12 | PF00899 | 0.647 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.388 |
LIG_WRPW_2 | 279 | 282 | PF00400 | 0.424 |
LIG_WW_3 | 195 | 199 | PF00397 | 0.506 |
LIG_WW_3 | 597 | 601 | PF00397 | 0.765 |
MOD_CDC14_SPxK_1 | 479 | 482 | PF00782 | 0.686 |
MOD_CDK_SPxK_1 | 476 | 482 | PF00069 | 0.685 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.402 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.622 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.557 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.626 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.554 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.666 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.735 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.697 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.614 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.612 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.742 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.498 |
MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.460 |
MOD_GlcNHglycan | 118 | 122 | PF01048 | 0.520 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.660 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.394 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.424 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.578 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.613 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.571 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.632 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.562 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.555 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.495 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.685 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.726 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.537 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.689 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.544 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.375 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.491 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.594 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.617 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.680 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.513 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.518 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.387 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.655 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.710 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.671 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.749 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.611 |
MOD_LATS_1 | 517 | 523 | PF00433 | 0.726 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.563 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.366 |
MOD_N-GLC_1 | 503 | 508 | PF02516 | 0.739 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.324 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.478 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.686 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.437 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.222 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.559 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.703 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.353 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.497 |
MOD_PIKK_1 | 544 | 550 | PF00454 | 0.755 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.666 |
MOD_PK_1 | 526 | 532 | PF00069 | 0.541 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.514 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.340 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.584 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.716 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.782 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.509 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.570 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.429 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.366 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.678 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.460 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.350 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.425 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.366 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.394 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.479 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.706 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.742 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.709 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.606 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.366 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.493 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.659 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.758 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.746 |
TRG_DiLeu_BaEn_1 | 144 | 149 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 296 | 301 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.201 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.142 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.768 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYD2 | Leptomonas seymouri | 52% | 100% |
A0A0S4ITU3 | Bodo saltans | 43% | 100% |
A0A3R7KE78 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H711 | Leishmania donovani | 100% | 100% |
A4H947 | Leishmania braziliensis | 81% | 100% |
C9ZP39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AR56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QEA7 | Leishmania major | 94% | 100% |
Q5ZLM2 | Gallus gallus | 34% | 100% |