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. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 24 |
GO:0032991 | protein-containing complex | 1 | 24 |
GO:0043226 | organelle | 2 | 24 |
GO:0043228 | non-membrane-bounded organelle | 3 | 24 |
GO:0043229 | intracellular organelle | 3 | 24 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 24 |
GO:0110165 | cellular anatomical entity | 1 | 24 |
GO:1990904 | ribonucleoprotein complex | 2 | 24 |
GO:0005730 | nucleolus | 5 | 6 |
GO:0097361 | CIA complex | 3 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
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 |
Related structures:
AlphaFold database: A4H4H1
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 4 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 4 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 4 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 4 |
GO:0006396 | RNA processing | 6 | 4 |
GO:0006397 | mRNA processing | 7 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0008380 | RNA splicing | 7 | 4 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 4 |
GO:0016071 | mRNA metabolic process | 6 | 4 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0046483 | heterocycle metabolic process | 3 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090304 | nucleic acid metabolic process | 4 | 4 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 4 |
GO:0006790 | sulfur compound metabolic process | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 1 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.748 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.376 |
DEG_SPOP_SBC_1 | 438 | 442 | PF00917 | 0.508 |
DOC_MAPK_gen_1 | 123 | 130 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 23 | 33 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 248 | 257 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 285 | 293 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 3 | 10 | PF00069 | 0.427 |
DOC_MAPK_HePTP_8 | 283 | 295 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 24 | 33 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 248 | 257 | PF00069 | 0.610 |
DOC_MAPK_MEF2A_6 | 286 | 295 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 3 | 10 | PF00069 | 0.433 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.634 |
DOC_USP7_MATH_2 | 151 | 157 | PF00917 | 0.406 |
DOC_USP7_UBL2_3 | 168 | 172 | PF12436 | 0.467 |
DOC_USP7_UBL2_3 | 174 | 178 | PF12436 | 0.565 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.439 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.541 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 347 | 356 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 437 | 447 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 585 | 590 | PF00244 | 0.563 |
LIG_APCC_ABBA_1 | 310 | 315 | PF00400 | 0.385 |
LIG_APCC_ABBA_1 | 62 | 67 | PF00400 | 0.551 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.462 |
LIG_BRCT_BRCA1_1 | 427 | 431 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 511 | 515 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.414 |
LIG_deltaCOP1_diTrp_1 | 614 | 620 | PF00928 | 0.449 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.602 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.492 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.563 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.491 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.583 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.471 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.507 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.614 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.612 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.333 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.489 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.374 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.346 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.460 |
LIG_Integrin_RGD_1 | 392 | 394 | PF01839 | 0.233 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 553 | 559 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 570 | 581 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 612 | 619 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.405 |
LIG_Pex14_1 | 555 | 559 | PF04695 | 0.449 |
LIG_Pex14_1 | 660 | 664 | PF04695 | 0.263 |
LIG_Pex14_2 | 511 | 515 | PF04695 | 0.449 |
LIG_PTB_Apo_2 | 308 | 315 | PF02174 | 0.337 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 364 | 367 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.550 |
LIG_SH2_STAT3 | 352 | 355 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.449 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.568 |
LIG_SH3_5 | 475 | 479 | PF00018 | 0.410 |
LIG_SUMO_SIM_par_1 | 138 | 145 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 299 | 308 | PF11976 | 0.501 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.519 |
LIG_TYR_ITIM | 114 | 119 | PF00017 | 0.559 |
LIG_UBA3_1 | 28 | 34 | PF00899 | 0.384 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.464 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 43 | 48 | PF05994 | 0.535 |
LIG_WRC_WIRS_1 | 458 | 463 | PF05994 | 0.406 |
MOD_CDC14_SPxK_1 | 240 | 243 | PF00782 | 0.541 |
MOD_CDK_SPK_2 | 387 | 392 | PF00069 | 0.508 |
MOD_CDK_SPK_2 | 429 | 434 | PF00069 | 0.457 |
MOD_CDK_SPxK_1 | 237 | 243 | PF00069 | 0.544 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.456 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.509 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.467 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.498 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.406 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.484 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.557 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.472 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.843 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.686 |
MOD_Cter_Amidation | 121 | 124 | PF01082 | 0.435 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.482 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.444 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.567 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.645 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.641 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.510 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.536 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.399 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.280 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.295 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.287 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.476 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.332 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.688 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.678 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.491 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.605 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.620 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.438 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.423 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.448 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.386 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.570 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.479 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.502 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.441 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.548 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.543 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.477 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.589 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.587 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.491 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.757 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.519 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.372 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.389 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.456 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.537 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.607 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.604 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.309 |
MOD_NEK2_2 | 142 | 147 | PF00069 | 0.509 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.406 |
MOD_NEK2_2 | 485 | 490 | PF00069 | 0.447 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.396 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.599 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.510 |
MOD_PK_1 | 11 | 17 | PF00069 | 0.399 |
MOD_PK_1 | 613 | 619 | PF00069 | 0.508 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.592 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.355 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.355 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.469 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.483 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.499 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.563 |
MOD_Plk_1 | 613 | 619 | PF00069 | 0.496 |
MOD_Plk_2-3 | 153 | 159 | PF00069 | 0.591 |
MOD_Plk_2-3 | 278 | 284 | PF00069 | 0.438 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.660 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.591 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.497 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.406 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.482 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.460 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.597 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.397 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.296 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.802 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.521 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.481 |
MOD_SUMO_for_1 | 322 | 325 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 278 | 287 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 537 | 547 | PF00179 | 0.252 |
MOD_SUMO_rev_2 | 602 | 608 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 63 | 71 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 651 | 657 | PF00179 | 0.364 |
MOD_SUMO_rev_2 | 97 | 102 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.429 |
TRG_NES_CRM1_1 | 27 | 39 | PF08389 | 0.415 |
TRG_NLS_MonoExtN_4 | 168 | 175 | PF00514 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBF5 | Leptomonas seymouri | 63% | 96% |
A0A0S4JTE0 | Bodo saltans | 42% | 88% |
A0A0S4KJ87 | Bodo saltans | 24% | 100% |
A0A1X0NK47 | Trypanosomatidae | 47% | 95% |
A0A3Q8IGC4 | Leishmania donovani | 27% | 100% |
A0A3R7K7N9 | Trypanosoma rangeli | 46% | 95% |
A0A3S5H5M7 | Leishmania donovani | 67% | 99% |
A0A3S7XBP3 | Leishmania donovani | 27% | 100% |
A4HDT7 | Leishmania braziliensis | 27% | 100% |
A4HL42 | Leishmania braziliensis | 25% | 100% |
A4HPZ9 | Leishmania braziliensis | 26% | 100% |
A4HSP6 | Leishmania infantum | 67% | 99% |
A4I135 | Leishmania infantum | 27% | 100% |
A4IDR0 | Leishmania infantum | 27% | 100% |
C9ZT89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 95% |
E9AKN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 99% |
E9ATR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P53699 | Candida albicans | 23% | 97% |
Q4Q0T1 | Leishmania major | 27% | 100% |
Q4QAA4 | Leishmania major | 27% | 100% |
Q4QJ76 | Leishmania major | 65% | 100% |
V5BDR9 | Trypanosoma cruzi | 47% | 97% |