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:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X3Z9
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003747 | translation release factor activity | 5 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0008079 | translation termination factor activity | 4 | 3 |
GO:0008135 | translation factor activity, RNA binding | 3 | 3 |
GO:0045182 | translation regulator activity | 1 | 3 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.470 |
CLV_PCSK_FUR_1 | 194 | 198 | PF00082 | 0.527 |
CLV_PCSK_FUR_1 | 89 | 93 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.612 |
CLV_PCSK_PC7_1 | 194 | 200 | PF00082 | 0.505 |
CLV_PCSK_PC7_1 | 33 | 39 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.497 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.437 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.662 |
DOC_MAPK_gen_1 | 100 | 109 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 154 | 163 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 165 | 176 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 218 | 228 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 438 | 447 | PF00069 | 0.751 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.494 |
DOC_MAPK_HePTP_8 | 151 | 163 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 169 | 176 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 383 | 391 | PF00069 | 0.523 |
DOC_MAPK_NFAT4_5 | 169 | 177 | PF00069 | 0.428 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 137 | 147 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 200 | 206 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 328 | 338 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 380 | 390 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 45 | 55 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 9 | 13 | PF00244 | 0.626 |
LIG_Actin_WH2_2 | 330 | 345 | PF00022 | 0.522 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 9 | 13 | PF00533 | 0.755 |
LIG_BRCT_BRCA1_2 | 105 | 111 | PF00533 | 0.506 |
LIG_CSL_BTD_1 | 266 | 269 | PF09270 | 0.523 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.423 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.452 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.672 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.716 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.570 |
LIG_LIR_Apic_2 | 102 | 108 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.436 |
LIG_Pex14_1 | 386 | 390 | PF04695 | 0.487 |
LIG_Pex14_2 | 158 | 162 | PF04695 | 0.430 |
LIG_Pex14_2 | 334 | 338 | PF04695 | 0.377 |
LIG_REV1ctd_RIR_1 | 112 | 120 | PF16727 | 0.431 |
LIG_REV1ctd_RIR_1 | 406 | 415 | PF16727 | 0.435 |
LIG_RPA_C_Fungi | 160 | 172 | PF08784 | 0.473 |
LIG_RPA_C_Insects | 160 | 175 | PF08784 | 0.513 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.500 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 105 | 109 | PF00017 | 0.535 |
LIG_SH2_SRC | 303 | 306 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.368 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.648 |
LIG_SUMO_SIM_anti_2 | 77 | 83 | PF11976 | 0.426 |
LIG_TYR_ITSM | 100 | 107 | PF00017 | 0.600 |
LIG_UBA3_1 | 81 | 90 | PF00899 | 0.568 |
MOD_CDK_SPxxK_3 | 396 | 403 | PF00069 | 0.464 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.722 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.688 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.575 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.498 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.571 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.473 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.568 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.555 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.565 |
MOD_GlcNHglycan | 412 | 416 | PF01048 | 0.344 |
MOD_GlcNHglycan | 417 | 421 | PF01048 | 0.461 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.718 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.608 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.400 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.586 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.548 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.754 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.721 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.700 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.645 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.590 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.568 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.615 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.369 |
MOD_NEK2_2 | 8 | 13 | PF00069 | 0.711 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.589 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.577 |
MOD_PK_1 | 103 | 109 | PF00069 | 0.568 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.568 |
MOD_PKA_1 | 439 | 445 | PF00069 | 0.546 |
MOD_PKA_1 | 59 | 65 | PF00069 | 0.609 |
MOD_PKA_1 | 91 | 97 | PF00069 | 0.652 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.568 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.571 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.467 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.688 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.591 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.565 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.476 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.591 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.419 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.541 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.722 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.567 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.456 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.721 |
MOD_SUMO_for_1 | 409 | 412 | PF00179 | 0.535 |
MOD_SUMO_rev_2 | 106 | 114 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 117 | 125 | PF00179 | 0.376 |
MOD_SUMO_rev_2 | 62 | 69 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.686 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 327 | 329 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.661 |
TRG_NLS_MonoCore_2 | 88 | 93 | PF00514 | 0.598 |
TRG_NLS_MonoExtC_3 | 89 | 95 | PF00514 | 0.622 |
TRG_NLS_MonoExtN_4 | 88 | 94 | PF00514 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ29 | Leptomonas seymouri | 61% | 98% |
A0A0S4JPR1 | Bodo saltans | 33% | 84% |
A0A1X0P2E4 | Trypanosomatidae | 39% | 97% |
A0A3R7MQL4 | Trypanosoma rangeli | 45% | 95% |
A4HIU0 | Leishmania braziliensis | 80% | 100% |
A4I645 | Leishmania infantum | 100% | 100% |
C9ZRG6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 97% |
E9B1C8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q6T4 | Leishmania major | 93% | 100% |
V5BX14 | Trypanosoma cruzi | 41% | 94% |