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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0005840 | ribosome | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005847 | mRNA cleavage and polyadenylation specificity factor complex | 4 | 1 |
GO:0005849 | mRNA cleavage factor complex | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HHZ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016071 | mRNA metabolic process | 6 | 12 |
GO:0031123 | RNA 3'-end processing | 7 | 12 |
GO:0031124 | mRNA 3'-end processing | 8 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.694 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.694 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.499 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.475 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.338 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.717 |
DOC_ANK_TNKS_1 | 327 | 334 | PF00023 | 0.517 |
DOC_CKS1_1 | 133 | 138 | PF01111 | 0.474 |
DOC_MAPK_gen_1 | 188 | 194 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 180 | 187 | PF00149 | 0.317 |
DOC_PP1_RVXF_1 | 221 | 228 | PF00149 | 0.317 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.311 |
DOC_PP1_RVXF_1 | 62 | 69 | PF00149 | 0.514 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.627 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.316 |
DOC_USP7_UBL2_3 | 421 | 425 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.322 |
LIG_14-3-3_CanoR_1 | 148 | 158 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 43 | 51 | PF00244 | 0.677 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.732 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.511 |
LIG_CSL_BTD_1 | 433 | 436 | PF09270 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 224 | 234 | PF00928 | 0.335 |
LIG_eIF4E_1 | 96 | 102 | PF01652 | 0.531 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.208 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.445 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.496 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.418 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.674 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.431 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.308 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.539 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.492 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.444 |
LIG_LIR_Apic_2 | 67 | 71 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 207 | 215 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.354 |
LIG_PCNA_yPIPBox_3 | 74 | 83 | PF02747 | 0.453 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.337 |
LIG_Pex14_2 | 26 | 30 | PF04695 | 0.547 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.698 |
LIG_PTB_Apo_2 | 205 | 212 | PF02174 | 0.488 |
LIG_SH2_CRK | 288 | 292 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.509 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.454 |
LIG_SH3_2 | 38 | 43 | PF14604 | 0.682 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.676 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.436 |
LIG_TYR_ITIM | 389 | 394 | PF00017 | 0.383 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.611 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.344 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.324 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.540 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.395 |
MOD_Cter_Amidation | 145 | 148 | PF01082 | 0.332 |
MOD_Cter_Amidation | 186 | 189 | PF01082 | 0.509 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.446 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.656 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.291 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.335 |
MOD_GlcNHglycan | 25 | 29 | PF01048 | 0.712 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.280 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.290 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.335 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.290 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.404 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.355 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.220 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.547 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.434 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.296 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.332 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.292 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.465 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.316 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.252 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.337 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.280 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.322 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.252 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.346 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.532 |
MOD_PKA_1 | 358 | 364 | PF00069 | 0.513 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.398 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.532 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.513 |
MOD_PKB_1 | 42 | 50 | PF00069 | 0.701 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.348 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.325 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.357 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.484 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.482 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.314 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.560 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.328 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.379 |
MOD_SUMO_rev_2 | 165 | 173 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 226 | 234 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 269 | 273 | PF00179 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 58 | 63 | PF00026 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHN2 | Leptomonas seymouri | 23% | 92% |
A0A0N1PBX5 | Leptomonas seymouri | 88% | 100% |
A0A0S4JFE0 | Bodo saltans | 54% | 100% |
A0A0S4JRK0 | Bodo saltans | 23% | 83% |
A0A0S4KJ87 | Bodo saltans | 23% | 80% |
A0A1X0NVZ7 | Trypanosomatidae | 23% | 92% |
A0A1X0P2X5 | Trypanosomatidae | 63% | 100% |
A0A3Q8IE21 | Leishmania donovani | 92% | 98% |
A0A3Q8IGC4 | Leishmania donovani | 25% | 92% |
A0A3R7N6M9 | Trypanosoma rangeli | 23% | 92% |
A0A3R7NRU0 | Trypanosoma rangeli | 63% | 100% |
A4HDT7 | Leishmania braziliensis | 24% | 92% |
A4I135 | Leishmania infantum | 25% | 92% |
A4I569 | Leishmania infantum | 93% | 100% |
B5X212 | Salmo salar | 24% | 100% |
B5X9P2 | Salmo salar | 22% | 100% |
C9ZQJ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
C9ZW72 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 78% |
E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 92% |
E9B0G6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
O76071 | Homo sapiens | 22% | 100% |
P0CS46 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 26% | 67% |
P0CS47 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 26% | 67% |
P42841 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q28DW0 | Xenopus tropicalis | 22% | 100% |
Q2TZG4 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 30% | 79% |
Q4I7X1 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 27% | 78% |
Q4Q7R7 | Leishmania major | 93% | 100% |
Q4QAA4 | Leishmania major | 25% | 92% |
Q4X1Y0 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 29% | 94% |
Q58D20 | Bos taurus | 24% | 99% |
Q59WJ4 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 88% |
Q5AZX0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 84% |
Q5DFU0 | Schistosoma japonicum | 23% | 100% |
Q5M7T1 | Rattus norvegicus | 23% | 100% |
Q5RFF8 | Pongo abelii | 23% | 99% |
Q6BVZ3 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 28% | 95% |
Q6CGP9 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 90% |
Q6CP71 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 30% | 100% |
Q6FJS0 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 29% | 100% |
Q6NLV4 | Arabidopsis thaliana | 32% | 74% |
Q75AV4 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 28% | 100% |
Q75C26 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 24% | 100% |
Q7RY68 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 73% |
Q7T0P4 | Xenopus laevis | 23% | 100% |
Q8VEJ4 | Mus musculus | 24% | 99% |
Q9NVX2 | Homo sapiens | 24% | 99% |
Q9UTN4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 94% |
V5DD51 | Trypanosoma cruzi | 62% | 100% |