Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
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. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 17 |
GO:0032991 | protein-containing complex | 1 | 17 |
GO:0043226 | organelle | 2 | 17 |
GO:0043228 | non-membrane-bounded organelle | 3 | 17 |
GO:0043229 | intracellular organelle | 3 | 17 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
GO:1990904 | ribonucleoprotein complex | 2 | 17 |
GO:0000974 | Prp19 complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:0097361 | CIA complex | 3 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
Related structures:
AlphaFold database: A0A3S5H5M7
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 3 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 3 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 3 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006397 | mRNA processing | 7 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0008380 | RNA splicing | 7 | 3 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016071 | mRNA metabolic process | 6 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:0006790 | sulfur compound metabolic process | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 526 | 530 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.836 |
CLV_PCSK_PC7_1 | 238 | 244 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 657 | 661 | PF00082 | 0.436 |
DEG_SCF_FBW7_1 | 278 | 285 | PF00400 | 0.474 |
DEG_SPOP_SBC_1 | 448 | 452 | PF00917 | 0.573 |
DOC_ANK_TNKS_1 | 356 | 363 | PF00023 | 0.581 |
DOC_CKS1_1 | 279 | 284 | PF01111 | 0.484 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 126 | 133 | PF00069 | 0.634 |
DOC_MAPK_gen_1 | 23 | 33 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 295 | 305 | PF00069 | 0.574 |
DOC_MAPK_HePTP_8 | 255 | 267 | PF00069 | 0.690 |
DOC_MAPK_HePTP_8 | 293 | 305 | PF00069 | 0.629 |
DOC_MAPK_MEF2A_6 | 24 | 33 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 258 | 267 | PF00069 | 0.696 |
DOC_MAPK_MEF2A_6 | 296 | 305 | PF00069 | 0.638 |
DOC_PP1_RVXF_1 | 3 | 9 | PF00149 | 0.473 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.883 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.629 |
DOC_USP7_UBL2_3 | 291 | 295 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 296 | 300 | PF12436 | 0.457 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.508 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.609 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 447 | 457 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 514 | 519 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 595 | 600 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 631 | 638 | PF00244 | 0.384 |
LIG_APCC_ABBA_1 | 320 | 325 | PF00400 | 0.563 |
LIG_APCC_ABBA_1 | 62 | 67 | PF00400 | 0.624 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.521 |
LIG_BIR_III_4 | 184 | 188 | PF00653 | 0.600 |
LIG_BRCT_BRCA1_1 | 521 | 525 | PF00533 | 0.517 |
LIG_deltaCOP1_diTrp_1 | 624 | 630 | PF00928 | 0.507 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.666 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.626 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.660 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.667 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.642 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.512 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.615 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.518 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.378 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.403 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.550 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.536 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.631 |
LIG_GBD_Chelix_1 | 320 | 328 | PF00786 | 0.504 |
LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 285 | 293 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 563 | 569 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 580 | 591 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 624 | 629 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 563 | 568 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.446 |
LIG_NRP_CendR_1 | 673 | 675 | PF00754 | 0.444 |
LIG_Pex14_1 | 565 | 569 | PF04695 | 0.507 |
LIG_Pex14_2 | 521 | 525 | PF04695 | 0.507 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.517 |
LIG_SH2_GRB2like | 374 | 377 | PF00017 | 0.580 |
LIG_SH2_PTP2 | 119 | 122 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 583 | 587 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 617 | 620 | PF00017 | 0.507 |
LIG_SH3_1 | 238 | 244 | PF00018 | 0.594 |
LIG_SH3_2 | 342 | 347 | PF14604 | 0.600 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.430 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.697 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.587 |
LIG_SUMO_SIM_par_1 | 38 | 45 | PF11976 | 0.399 |
LIG_TRAF2_1 | 135 | 138 | PF00917 | 0.490 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.584 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.633 |
LIG_UBA3_1 | 28 | 34 | PF00899 | 0.445 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.531 |
LIG_WRC_WIRS_1 | 43 | 48 | PF05994 | 0.607 |
MOD_CDK_SPK_2 | 397 | 402 | PF00069 | 0.573 |
MOD_CDK_SPK_2 | 439 | 444 | PF00069 | 0.517 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.558 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.570 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.515 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.618 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.546 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.581 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.657 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.576 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.548 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.464 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.482 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.640 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.788 |
MOD_Cter_Amidation | 124 | 127 | PF01082 | 0.515 |
MOD_Cter_Amidation | 297 | 300 | PF01082 | 0.527 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.556 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.691 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.705 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.631 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.299 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.336 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.347 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.363 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.675 |
MOD_GlcNHglycan | 85 | 89 | PF01048 | 0.767 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.766 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.649 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.588 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.405 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.492 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.504 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.455 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.632 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.535 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.588 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.532 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.452 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.526 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.501 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.635 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.670 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.594 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.569 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.419 |
MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.314 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.666 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.538 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.570 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.597 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.818 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.785 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.638 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.560 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.660 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.540 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.598 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.638 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.363 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.580 |
MOD_NEK2_2 | 495 | 500 | PF00069 | 0.505 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.561 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.629 |
MOD_PK_1 | 623 | 629 | PF00069 | 0.573 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.708 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.675 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.781 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.384 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.480 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.558 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.514 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.507 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.546 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.547 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.526 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.659 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.459 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.529 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.408 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.443 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.523 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.486 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.481 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.327 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.498 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.530 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.540 |
MOD_SUMO_rev_2 | 239 | 244 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 288 | 297 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 325 | 335 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 652 | 659 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 661 | 667 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 67 | 76 | PF00179 | 0.563 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_1 | 553 | 558 | PF01217 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.645 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.612 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 672 | 675 | PF00400 | 0.519 |
TRG_NES_CRM1_1 | 27 | 39 | PF08389 | 0.485 |
TRG_NES_CRM1_1 | 318 | 331 | PF08389 | 0.561 |
TRG_NLS_MonoExtN_4 | 332 | 337 | PF00514 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBF5 | Leptomonas seymouri | 67% | 98% |
A0A0S4JTE0 | Bodo saltans | 42% | 89% |
A0A0S4KJ87 | Bodo saltans | 25% | 100% |
A0A1X0NK47 | Trypanosomatidae | 50% | 96% |
A0A3R7K7N9 | Trypanosoma rangeli | 49% | 97% |
A0A3S7XBP3 | Leishmania donovani | 26% | 100% |
A4H4H1 | Leishmania braziliensis | 67% | 99% |
A4HPZ9 | Leishmania braziliensis | 25% | 100% |
A4HSP6 | Leishmania infantum | 99% | 100% |
A4IDR0 | Leishmania infantum | 26% | 100% |
C9ZT89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 97% |
D4AM37 | Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) | 24% | 100% |
D4D8P3 | Trichophyton verrucosum (strain HKI 0517) | 24% | 100% |
E9AKN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q0T1 | Leishmania major | 26% | 100% |
Q4QJ76 | Leishmania major | 89% | 100% |
V5BDR9 | Trypanosoma cruzi | 51% | 98% |