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: E9B558
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.553 |
CLV_MEL_PAP_1 | 232 | 238 | PF00089 | 0.537 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.583 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.530 |
DEG_APCC_DBOX_1 | 424 | 432 | PF00400 | 0.594 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.766 |
DOC_CKS1_1 | 64 | 69 | PF01111 | 0.566 |
DOC_CYCLIN_yCln2_LP_2 | 64 | 70 | PF00134 | 0.542 |
DOC_MAPK_gen_1 | 226 | 234 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 415 | 423 | PF00069 | 0.672 |
DOC_MAPK_gen_1 | 444 | 454 | PF00069 | 0.661 |
DOC_MAPK_MEF2A_6 | 228 | 236 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 447 | 456 | PF00069 | 0.684 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.579 |
DOC_PP4_FxxP_1 | 518 | 521 | PF00568 | 0.348 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 226 | 234 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 363 | 371 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 373 | 379 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 469 | 478 | PF00244 | 0.506 |
LIG_APCC_ABBA_1 | 452 | 457 | PF00400 | 0.679 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.682 |
LIG_BIR_III_2 | 322 | 326 | PF00653 | 0.726 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.584 |
LIG_CSL_BTD_1 | 534 | 537 | PF09270 | 0.442 |
LIG_EH1_1 | 43 | 51 | PF00400 | 0.576 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.488 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.432 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.330 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.405 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.722 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.518 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.445 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.477 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.573 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.629 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.449 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.475 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.685 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.825 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.622 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.569 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.539 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.628 |
LIG_HCF-1_HBM_1 | 244 | 247 | PF13415 | 0.577 |
LIG_MLH1_MIPbox_1 | 452 | 456 | PF16413 | 0.584 |
LIG_Pex14_2 | 378 | 382 | PF04695 | 0.566 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.721 |
LIG_SH2_GRB2like | 181 | 184 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.585 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.683 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.581 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.489 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.760 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.674 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.693 |
LIG_SUMO_SIM_par_1 | 268 | 274 | PF11976 | 0.453 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.449 |
LIG_UBA3_1 | 49 | 56 | PF00899 | 0.476 |
LIG_WW_3 | 357 | 361 | PF00397 | 0.729 |
LIG_WW_3 | 466 | 470 | PF00397 | 0.697 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.572 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.695 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.476 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.710 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.512 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.652 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.650 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.690 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.449 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.430 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.537 |
MOD_Cter_Amidation | 413 | 416 | PF01082 | 0.732 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.523 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.475 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.335 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.446 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.695 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.638 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.444 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.530 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.406 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.592 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.712 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.327 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.409 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.623 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.726 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.693 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.496 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.609 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.468 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.366 |
MOD_LATS_1 | 306 | 312 | PF00433 | 0.738 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.595 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.402 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.405 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.511 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.579 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.768 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.495 |
MOD_NEK2_2 | 181 | 186 | PF00069 | 0.449 |
MOD_NEK2_2 | 528 | 533 | PF00069 | 0.410 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.584 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.631 |
MOD_PK_1 | 308 | 314 | PF00069 | 0.636 |
MOD_PKA_1 | 469 | 475 | PF00069 | 0.557 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.631 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.535 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.542 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.388 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.511 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.648 |
MOD_Plk_1 | 450 | 456 | PF00069 | 0.617 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.394 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.460 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.518 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.592 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.582 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.653 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.795 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.756 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.711 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.505 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.567 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.701 |
TRG_DiLeu_BaEn_1 | 473 | 478 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.703 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 469 | 473 | PF00026 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 71 | 76 | PF00026 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6E9 | Leptomonas seymouri | 67% | 95% |
A0A0S4JQH6 | Bodo saltans | 35% | 100% |
A0A1X0P9Q5 | Trypanosomatidae | 42% | 100% |
A0A3Q8IUQ4 | Leishmania donovani | 93% | 99% |
A0A3R7L5W7 | Trypanosoma rangeli | 42% | 100% |
A4HAY5 | Leishmania braziliensis | 85% | 100% |
A4IA44 | Leishmania infantum | 93% | 99% |
C9ZM56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
Q4Q2S7 | Leishmania major | 94% | 99% |
V5BKS0 | Trypanosoma cruzi | 45% | 100% |