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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IUQ4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 234 | 240 | PF00089 | 0.537 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.587 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.508 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.529 |
DEG_APCC_DBOX_1 | 430 | 438 | PF00400 | 0.590 |
DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.767 |
DOC_ANK_TNKS_1 | 420 | 427 | PF00023 | 0.583 |
DOC_CKS1_1 | 64 | 69 | PF01111 | 0.573 |
DOC_CYCLIN_yCln2_LP_2 | 64 | 70 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 421 | 429 | PF00069 | 0.646 |
DOC_MAPK_gen_1 | 450 | 460 | PF00069 | 0.653 |
DOC_MAPK_MEF2A_6 | 230 | 238 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 421 | 429 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.695 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.583 |
DOC_MAPK_NFAT4_5 | 422 | 430 | PF00069 | 0.542 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.510 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 250 | 255 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 369 | 377 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 475 | 484 | PF00244 | 0.457 |
LIG_APCC_ABBA_1 | 458 | 463 | PF00400 | 0.717 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.680 |
LIG_BIR_III_2 | 328 | 332 | PF00653 | 0.707 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.631 |
LIG_CSL_BTD_1 | 540 | 543 | PF09270 | 0.437 |
LIG_EH1_1 | 43 | 51 | PF00400 | 0.579 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.491 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.487 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.477 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.415 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.511 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.439 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.476 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.573 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.669 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.445 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.656 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.773 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.650 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.573 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.483 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.654 |
LIG_HCF-1_HBM_1 | 246 | 249 | PF13415 | 0.580 |
LIG_MLH1_MIPbox_1 | 458 | 462 | PF16413 | 0.631 |
LIG_MYND_1 | 303 | 307 | PF01753 | 0.594 |
LIG_Pex14_2 | 384 | 388 | PF04695 | 0.562 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.725 |
LIG_SH2_GRB2like | 183 | 186 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.687 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.547 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.489 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.764 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.686 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.693 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.428 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.562 |
LIG_UBA3_1 | 49 | 56 | PF00899 | 0.481 |
LIG_WW_2 | 303 | 306 | PF00397 | 0.593 |
LIG_WW_3 | 363 | 367 | PF00397 | 0.740 |
LIG_WW_3 | 472 | 476 | PF00397 | 0.653 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.700 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.470 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.687 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.650 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.514 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.658 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.692 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.559 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.427 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.514 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.748 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.582 |
MOD_Cter_Amidation | 419 | 422 | PF01082 | 0.730 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.520 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.571 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.290 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.442 |
MOD_GlcNHglycan | 3 | 7 | PF01048 | 0.635 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.689 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.659 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.422 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.562 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.410 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.715 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.470 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.408 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.662 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.563 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.608 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.495 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.466 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.370 |
MOD_LATS_1 | 312 | 318 | PF00433 | 0.727 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.728 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.515 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.382 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.524 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.573 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.770 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.484 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.562 |
MOD_NEK2_2 | 534 | 539 | PF00069 | 0.410 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.583 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.630 |
MOD_PK_1 | 314 | 320 | PF00069 | 0.620 |
MOD_PKA_1 | 475 | 481 | PF00069 | 0.493 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.649 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.482 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.546 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.584 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.519 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.698 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.506 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.628 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.393 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.437 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.512 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.565 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.530 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.697 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.799 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.488 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.567 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.704 |
TRG_DiLeu_BaEn_1 | 479 | 484 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.680 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 474 | 476 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 71 | 76 | PF00026 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6E9 | Leptomonas seymouri | 68% | 96% |
A0A0S4JQH6 | Bodo saltans | 34% | 100% |
A0A1X0P9Q5 | Trypanosomatidae | 42% | 100% |
A0A3R7L5W7 | Trypanosoma rangeli | 40% | 100% |
A4HAY5 | Leishmania braziliensis | 85% | 99% |
A4IA44 | Leishmania infantum | 99% | 100% |
C9ZM56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B558 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
Q4Q2S7 | Leishmania major | 93% | 99% |
V5BKS0 | Trypanosoma cruzi | 44% | 100% |