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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 15 |
GO:0032991 | protein-containing complex | 1 | 15 |
GO:0043226 | organelle | 2 | 15 |
GO:0043228 | non-membrane-bounded organelle | 3 | 15 |
GO:0043229 | intracellular organelle | 3 | 15 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:1990904 | ribonucleoprotein complex | 2 | 15 |
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:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0005730 | nucleolus | 5 | 5 |
Related structures:
AlphaFold database: E9B4L5
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 | 3 |
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 | 3 |
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:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 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 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 701 | 703 | PF00675 | 0.444 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.492 |
CLV_PCSK_PC7_1 | 436 | 442 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 444 | 452 | PF00400 | 0.476 |
DEG_SCF_FBW7_1 | 455 | 462 | PF00400 | 0.523 |
DEG_SPOP_SBC_1 | 185 | 189 | PF00917 | 0.518 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.463 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 648 | 656 | PF00134 | 0.438 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.325 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.348 |
DOC_PP1_RVXF_1 | 413 | 419 | PF00149 | 0.560 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.507 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.543 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.441 |
DOC_USP7_MATH_2 | 522 | 528 | PF00917 | 0.520 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.519 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 706 | 711 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 107 | 115 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 294 | 300 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 426 | 430 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 507 | 513 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 643 | 649 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 701 | 705 | PF00244 | 0.452 |
LIG_AP2alpha_2 | 13 | 15 | PF02296 | 0.443 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.546 |
LIG_BIR_III_4 | 264 | 268 | PF00653 | 0.463 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 522 | 526 | PF00533 | 0.524 |
LIG_CSL_BTD_1 | 101 | 104 | PF09270 | 0.664 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.687 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.447 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.472 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.534 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.443 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.634 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.579 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.606 |
LIG_HCF-1_HBM_1 | 146 | 149 | PF13415 | 0.277 |
LIG_LIR_Apic_2 | 286 | 290 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 212 | 219 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 633 | 644 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 182 | 186 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.481 |
LIG_MLH1_MIPbox_1 | 211 | 215 | PF16413 | 0.463 |
LIG_MYND_1 | 37 | 41 | PF01753 | 0.463 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.376 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.366 |
LIG_Rb_pABgroove_1 | 236 | 244 | PF01858 | 0.372 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.269 |
LIG_SH2_CRK | 636 | 640 | PF00017 | 0.457 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 688 | 692 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.493 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.433 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.481 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.447 |
LIG_TRAF2_1 | 620 | 623 | PF00917 | 0.474 |
LIG_WRC_WIRS_1 | 180 | 185 | PF05994 | 0.402 |
MOD_CDC14_SPxK_1 | 512 | 515 | PF00782 | 0.606 |
MOD_CDK_SPK_2 | 410 | 415 | PF00069 | 0.506 |
MOD_CDK_SPK_2 | 455 | 460 | PF00069 | 0.576 |
MOD_CDK_SPK_2 | 81 | 86 | PF00069 | 0.463 |
MOD_CDK_SPxK_1 | 509 | 515 | PF00069 | 0.603 |
MOD_CDK_SPxxK_3 | 408 | 415 | PF00069 | 0.558 |
MOD_CDK_SPxxK_3 | 509 | 516 | PF00069 | 0.606 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.502 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.486 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.744 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.565 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.544 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.688 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.493 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.582 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.653 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.609 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.578 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.605 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.547 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.265 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.374 |
MOD_GlcNHglycan | 243 | 247 | PF01048 | 0.336 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.288 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.278 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.587 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.500 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.618 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.290 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.404 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.640 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.603 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.543 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.280 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.532 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.525 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.596 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.286 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.477 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.461 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.491 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.539 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.470 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.569 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.534 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.606 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.593 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.541 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.495 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.602 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.607 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.570 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.568 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.609 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.569 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.272 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.588 |
MOD_N-GLC_1 | 597 | 602 | PF02516 | 0.542 |
MOD_N-GLC_2 | 124 | 126 | PF02516 | 0.473 |
MOD_N-GLC_2 | 473 | 475 | PF02516 | 0.602 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.553 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.429 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.498 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.345 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.477 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.337 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.401 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.595 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.460 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.421 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.527 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.674 |
MOD_PIKK_1 | 642 | 648 | PF00454 | 0.424 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.547 |
MOD_PKA_1 | 294 | 300 | PF00069 | 0.482 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.513 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.456 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.382 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.493 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.603 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.552 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.653 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.424 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.449 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.396 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.543 |
MOD_Plk_1 | 493 | 499 | PF00069 | 0.564 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.602 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.584 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.485 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.470 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.472 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.488 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.541 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.619 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.512 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.577 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.631 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.583 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.573 |
MOD_ProDKin_1 | 706 | 712 | PF00069 | 0.499 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.483 |
MOD_SUMO_rev_2 | 330 | 340 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 529 | 538 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 689 | 698 | PF00179 | 0.444 |
TRG_DiLeu_BaEn_1 | 625 | 630 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGC4 | Leishmania donovani | 24% | 100% |
A0A3Q8IKN8 | Leishmania donovani | 91% | 100% |
A0A3R7NL29 | Trypanosoma rangeli | 34% | 97% |
A0A3S7XBP3 | Leishmania donovani | 23% | 100% |
A4HAG2 | Leishmania braziliensis | 76% | 100% |
A4HDT7 | Leishmania braziliensis | 24% | 100% |
A4I135 | Leishmania infantum | 24% | 100% |
A4I9L7 | Leishmania infantum | 90% | 100% |
A4IDR0 | Leishmania infantum | 23% | 100% |
E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q0T1 | Leishmania major | 23% | 100% |
Q4Q3G1 | Leishmania major | 89% | 100% |
Q4QAA4 | Leishmania major | 24% | 100% |