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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
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 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4H4H3
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 16 |
GO:0003723 | RNA binding | 4 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0003729 | mRNA binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.389 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.413 |
DEG_APCC_DBOX_1 | 194 | 202 | PF00400 | 0.371 |
DEG_APCC_DBOX_1 | 268 | 276 | PF00400 | 0.414 |
DEG_MDM2_SWIB_1 | 364 | 371 | PF02201 | 0.335 |
DEG_SCF_FBW7_2 | 241 | 247 | PF00400 | 0.391 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.716 |
DOC_CKS1_1 | 241 | 246 | PF01111 | 0.391 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.610 |
DOC_CYCLIN_yCln2_LP_2 | 56 | 62 | PF00134 | 0.667 |
DOC_MAPK_gen_1 | 193 | 201 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 393 | 402 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 193 | 201 | PF00069 | 0.472 |
DOC_PP2B_LxvP_1 | 60 | 63 | PF13499 | 0.484 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.658 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.671 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.391 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.757 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 139 | 146 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 321 | 331 | PF00244 | 0.410 |
LIG_Actin_WH2_2 | 336 | 351 | PF00022 | 0.209 |
LIG_APCC_ABBA_1 | 249 | 254 | PF00400 | 0.455 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.633 |
LIG_BIR_III_2 | 20 | 24 | PF00653 | 0.686 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.763 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.746 |
LIG_EH1_1 | 341 | 349 | PF00400 | 0.354 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.702 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.687 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.404 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.546 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.641 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.747 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.756 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.383 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.623 |
LIG_GBD_Chelix_1 | 384 | 392 | PF00786 | 0.391 |
LIG_IBAR_NPY_1 | 104 | 106 | PF08397 | 0.536 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.657 |
LIG_LIR_Apic_2 | 313 | 317 | PF02991 | 0.448 |
LIG_LIR_Apic_2 | 462 | 468 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 130 | 138 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 175 | 186 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 352 | 361 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 414 | 418 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 432 | 436 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.651 |
LIG_PCNA_yPIPBox_3 | 389 | 401 | PF02747 | 0.435 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.403 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.499 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.448 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.506 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 132 | 136 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 314 | 318 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 43 | 47 | PF00017 | 0.683 |
LIG_SH2_NCK_1 | 437 | 441 | PF00017 | 0.445 |
LIG_SH2_PTP2 | 252 | 255 | PF00017 | 0.470 |
LIG_SH2_PTP2 | 354 | 357 | PF00017 | 0.511 |
LIG_SH2_SRC | 252 | 255 | PF00017 | 0.428 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.649 |
LIG_SH2_STAT3 | 116 | 119 | PF00017 | 0.653 |
LIG_SH2_STAT3 | 342 | 345 | PF00017 | 0.336 |
LIG_SH2_STAT3 | 418 | 421 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.448 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.511 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.765 |
LIG_SH3_4 | 316 | 323 | PF00018 | 0.391 |
LIG_SUMO_SIM_par_1 | 286 | 294 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.272 |
LIG_SUMO_SIM_par_1 | 79 | 85 | PF11976 | 0.511 |
LIG_TYR_ITIM | 435 | 440 | PF00017 | 0.440 |
LIG_UBA3_1 | 308 | 316 | PF00899 | 0.391 |
LIG_UBA3_1 | 330 | 336 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 361 | 366 | PF05994 | 0.516 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.624 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.595 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.648 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.711 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.552 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.693 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.631 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.558 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.673 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.724 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.770 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.597 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.383 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.698 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.605 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.439 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.591 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.448 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.462 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.634 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.602 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.680 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.573 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.610 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.624 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.644 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.716 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.479 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.443 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.639 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.708 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.666 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.675 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.490 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.349 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.503 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.458 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.473 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.323 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.397 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.485 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.422 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.693 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.730 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.422 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.341 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.695 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.698 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.541 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.791 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.273 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.507 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.503 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.691 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.607 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.643 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.449 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.453 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.409 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.691 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.710 |
TRG_DiLeu_BaLyEn_6 | 326 | 331 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 439 | 444 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.617 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.419 |
TRG_NES_CRM1_1 | 215 | 227 | PF08389 | 0.295 |
TRG_NES_CRM1_1 | 345 | 359 | PF08389 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSE0 | Leptomonas seymouri | 62% | 100% |
A0A0N1ILR0 | Leptomonas seymouri | 33% | 73% |
A0A0S4J2F9 | Bodo saltans | 46% | 100% |
A0A1X0NJM4 | Trypanosomatidae | 47% | 100% |
A0A3S5IQY1 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WPA1 | Leishmania donovani | 86% | 100% |
A4HSP8 | Leishmania infantum | 86% | 100% |
C9ZT94 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E8NHJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AKN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q4QCQ8 | Leishmania major | 33% | 100% |
Q4QJ74 | Leishmania major | 85% | 100% |
V5B968 | Trypanosoma cruzi | 48% | 100% |