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:0005815 | microtubule organizing center | 2 | 2 |
GO:0005840 | ribosome | 5 | 15 |
GO:0032991 | protein-containing complex | 1 | 15 |
GO:0036064 | ciliary basal body | 3 | 2 |
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:0005730 | nucleolus | 5 | 5 |
Related structures:
AlphaFold database: Q4Q3G1
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 2 |
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 |
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:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 608 | 612 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.772 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 696 | 698 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.683 |
DEG_SPOP_SBC_1 | 185 | 189 | PF00917 | 0.527 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.463 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 648 | 656 | PF00134 | 0.436 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.431 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.530 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.573 |
DOC_PP4_MxPP_1 | 410 | 413 | PF00568 | 0.520 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 107 | 115 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 294 | 300 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 389 | 397 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 426 | 430 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 476 | 482 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 507 | 513 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 643 | 649 | PF00244 | 0.650 |
LIG_AP2alpha_2 | 13 | 15 | PF02296 | 0.449 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.536 |
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 | 0.456 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.522 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.522 |
LIG_CSL_BTD_1 | 101 | 104 | PF09270 | 0.542 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.676 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.459 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.449 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.506 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.558 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.468 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.607 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.601 |
LIG_LIR_Gen_1 | 212 | 219 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 633 | 644 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 182 | 186 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.492 |
LIG_MLH1_MIPbox_1 | 211 | 215 | PF16413 | 0.463 |
LIG_MYND_1 | 37 | 41 | PF01753 | 0.463 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.435 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.375 |
LIG_Rb_pABgroove_1 | 236 | 244 | PF01858 | 0.379 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.287 |
LIG_SH2_CRK | 636 | 640 | PF00017 | 0.450 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 688 | 692 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 667 | 670 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.543 |
LIG_SH3_2 | 11 | 16 | PF14604 | 0.453 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.463 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.535 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.479 |
LIG_TRAF2_1 | 620 | 623 | PF00917 | 0.461 |
LIG_WRC_WIRS_1 | 180 | 185 | PF05994 | 0.415 |
MOD_CDC14_SPxK_1 | 512 | 515 | PF00782 | 0.601 |
MOD_CDK_SPK_2 | 81 | 86 | PF00069 | 0.297 |
MOD_CDK_SPxK_1 | 509 | 515 | PF00069 | 0.596 |
MOD_CDK_SPxxK_3 | 408 | 415 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 509 | 516 | PF00069 | 0.701 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.380 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.369 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.564 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.715 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.749 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.672 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.582 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.532 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.708 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.621 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.803 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.601 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.332 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.331 |
MOD_GlcNHglycan | 243 | 247 | PF01048 | 0.340 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.365 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.345 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.439 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.663 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.351 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.467 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.671 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.671 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.634 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.325 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.543 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.612 |
MOD_GlcNHglycan | 611 | 615 | PF01048 | 0.530 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.773 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.344 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.477 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.314 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.384 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.578 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.328 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.281 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.456 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.648 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.638 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.603 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.711 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.761 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.618 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.603 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.454 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.487 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.213 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.715 |
MOD_N-GLC_2 | 124 | 126 | PF02516 | 0.599 |
MOD_N-GLC_2 | 473 | 475 | PF02516 | 0.595 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.633 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.472 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.628 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.495 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.469 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.363 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.588 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.415 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.315 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.322 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.542 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.713 |
MOD_PIKK_1 | 642 | 648 | PF00454 | 0.421 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.352 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.620 |
MOD_PKA_1 | 294 | 300 | PF00069 | 0.683 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.525 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.488 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.499 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.503 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.688 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.536 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.575 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.632 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.649 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.471 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.427 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.380 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.529 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.641 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.606 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.380 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.562 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.360 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.434 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.630 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.621 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.669 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.658 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.545 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.340 |
MOD_SUMO_rev_2 | 330 | 340 | PF00179 | 0.312 |
MOD_SUMO_rev_2 | 529 | 538 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 689 | 698 | PF00179 | 0.433 |
TRG_DiLeu_BaEn_1 | 625 | 630 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.734 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBY0 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IGC4 | Leishmania donovani | 24% | 100% |
A0A3Q8IKN8 | Leishmania donovani | 93% | 100% |
A0A3R7NL29 | Trypanosoma rangeli | 33% | 97% |
A4HAG2 | Leishmania braziliensis | 76% | 99% |
A4HDT7 | Leishmania braziliensis | 24% | 100% |
A4I135 | Leishmania infantum | 24% | 100% |
A4I9L7 | Leishmania infantum | 93% | 100% |
D0A1X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
E9ATR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B4L5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QAA4 | Leishmania major | 24% | 100% |