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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E8NHJ3
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 19 |
GO:0003723 | RNA binding | 4 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
GO:0003729 | mRNA binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 420 | 424 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.629 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.409 |
CLV_Separin_Metazoa | 154 | 158 | PF03568 | 0.368 |
DEG_APCC_DBOX_1 | 101 | 109 | PF00400 | 0.397 |
DEG_APCC_DBOX_1 | 156 | 164 | PF00400 | 0.368 |
DEG_APCC_DBOX_1 | 227 | 235 | PF00400 | 0.479 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.498 |
DOC_CYCLIN_RxL_1 | 224 | 233 | PF00134 | 0.413 |
DOC_MAPK_FxFP_2 | 399 | 402 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 53 | 61 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 53 | 61 | PF00069 | 0.493 |
DOC_PP4_FxxP_1 | 399 | 402 | PF00568 | 0.757 |
DOC_PP4_FxxP_1 | 445 | 448 | PF00568 | 0.581 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.740 |
DOC_USP7_UBL2_3 | 286 | 290 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 11 | 18 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 185 | 193 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 36 | 46 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 407 | 415 | PF00244 | 0.568 |
LIG_Actin_WH2_1 | 227 | 244 | PF00022 | 0.414 |
LIG_Actin_WH2_1 | 39 | 57 | PF00022 | 0.430 |
LIG_Actin_WH2_2 | 40 | 57 | PF00022 | 0.428 |
LIG_EH1_1 | 251 | 259 | PF00400 | 0.431 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.494 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.711 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.379 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.571 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.402 |
LIG_LIR_Apic_2 | 397 | 402 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.415 |
LIG_PDZ_Class_2 | 448 | 453 | PF00595 | 0.508 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.646 |
LIG_SH2_STAT3 | 174 | 177 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.791 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.419 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.434 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.737 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.727 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.704 |
LIG_SUMO_SIM_par_1 | 256 | 262 | PF11976 | 0.226 |
LIG_UBA3_1 | 200 | 207 | PF00899 | 0.371 |
MOD_CDK_SPxxK_3 | 21 | 28 | PF00069 | 0.467 |
MOD_CDK_SPxxK_3 | 428 | 435 | PF00069 | 0.669 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.355 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.426 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.518 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.508 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.427 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.407 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.735 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.408 |
MOD_GlcNHglycan | 115 | 119 | PF01048 | 0.555 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.588 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.526 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.694 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.751 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.761 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.382 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.648 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.704 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.523 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.388 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.397 |
MOD_N-GLC_2 | 93 | 95 | PF02516 | 0.409 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.375 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.373 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.399 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.388 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.384 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.463 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.533 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.751 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.393 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.496 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.490 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.448 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.612 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.566 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.429 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.240 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.313 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.446 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.400 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.467 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.534 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.792 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.613 |
MOD_SUMO_for_1 | 285 | 288 | PF00179 | 0.466 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 273 | 276 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.441 |
TRG_NES_CRM1_1 | 158 | 169 | PF08389 | 0.368 |
TRG_NES_CRM1_1 | 49 | 60 | PF08389 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 227 | 232 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILR0 | Leptomonas seymouri | 60% | 69% |
A0A1X0NJM4 | Trypanosomatidae | 39% | 100% |
A0A1X0P8D8 | Trypanosomatidae | 22% | 79% |
A0A3Q8IA47 | Leishmania donovani | 94% | 77% |
A0A3R7NFN9 | Trypanosoma rangeli | 52% | 84% |
A0A3R7NHA6 | Trypanosoma rangeli | 26% | 79% |
A0A3S5IQY1 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WW64 | Leishmania donovani | 96% | 83% |
A4HYX9 | Leishmania infantum | 94% | 77% |
A4HYY0 | Leishmania infantum | 96% | 83% |
C9ZII7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 67% |
D0A2G7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 79% |
E9AIJ1 | Leishmania braziliensis | 83% | 100% |
E9ASC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 82% |
E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
Q4QCQ8 | Leishmania major | 74% | 96% |
Q4QCQ9 | Leishmania major | 92% | 100% |