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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AIJ1
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 | 18 |
GO:0003723 | RNA binding | 4 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
GO:0003729 | mRNA binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.416 |
CLV_Separin_Metazoa | 163 | 167 | PF03568 | 0.382 |
DEG_APCC_DBOX_1 | 110 | 118 | PF00400 | 0.409 |
DEG_APCC_DBOX_1 | 165 | 173 | PF00400 | 0.382 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.483 |
DEG_APCC_DBOX_1 | 375 | 383 | PF00400 | 0.521 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.380 |
DOC_CYCLIN_RxL_1 | 233 | 242 | PF00134 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 328 | 334 | PF00134 | 0.562 |
DOC_MAPK_FxFP_2 | 412 | 415 | PF00069 | 0.542 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.632 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.775 |
DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.643 |
DOC_USP7_UBL2_3 | 295 | 299 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 194 | 202 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 20 | 27 | PF00244 | 0.540 |
LIG_Actin_WH2_1 | 236 | 253 | PF00022 | 0.428 |
LIG_Actin_WH2_1 | 48 | 66 | PF00022 | 0.438 |
LIG_Actin_WH2_2 | 49 | 66 | PF00022 | 0.437 |
LIG_AP2alpha_2 | 178 | 180 | PF02296 | 0.290 |
LIG_BIR_III_4 | 69 | 73 | PF00653 | 0.195 |
LIG_CaM_IQ_9 | 287 | 303 | PF13499 | 0.455 |
LIG_EH1_1 | 260 | 268 | PF00400 | 0.434 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.373 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.565 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.437 |
LIG_LIR_Apic_2 | 410 | 415 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 410 | 414 | PF02991 | 0.454 |
LIG_PDZ_Class_2 | 462 | 467 | PF00595 | 0.514 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.650 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 183 | 186 | PF00017 | 0.347 |
LIG_SH2_STAT3 | 397 | 400 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.757 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.791 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.455 |
LIG_SH3_2 | 355 | 360 | PF14604 | 0.520 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.546 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.566 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.729 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.724 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.819 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.536 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.689 |
LIG_UBA3_1 | 209 | 216 | PF00899 | 0.371 |
MOD_CDK_SPxxK_3 | 30 | 37 | PF00069 | 0.458 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.665 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.481 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.377 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.521 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.394 |
MOD_GlcNHglycan | 124 | 128 | PF01048 | 0.542 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.522 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.696 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.403 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.752 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.388 |
MOD_N-GLC_2 | 102 | 104 | PF02516 | 0.391 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.411 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.404 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.527 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.392 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.419 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.396 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.685 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.583 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.519 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.477 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.438 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.511 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.670 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.435 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.559 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.404 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.458 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.663 |
MOD_SUMO_for_1 | 294 | 297 | PF00179 | 0.496 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.451 |
TRG_NES_CRM1_1 | 167 | 178 | PF08389 | 0.382 |
TRG_NES_CRM1_1 | 57 | 69 | PF08389 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 236 | 241 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 449 | 453 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P473 | Leptomonas seymouri | 23% | 84% |
A0A0N1ILR0 | Leptomonas seymouri | 56% | 71% |
A0A3Q8IA47 | Leishmania donovani | 85% | 79% |
A0A3R7NFN9 | Trypanosoma rangeli | 52% | 86% |
A0A3R7NHA6 | Trypanosoma rangeli | 24% | 82% |
A0A3S7WW64 | Leishmania donovani | 91% | 86% |
A4HNL0 | Leishmania braziliensis | 24% | 85% |
A4HYX9 | Leishmania infantum | 85% | 79% |
A4HYY0 | Leishmania infantum | 92% | 86% |
C9ZII7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 69% |
E8NHJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9ASC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 84% |
E9AUS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QCQ8 | Leishmania major | 90% | 100% |
Q4QCQ9 | Leishmania major | 82% | 100% |
V5B1W9 | Trypanosoma cruzi | 24% | 83% |