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. | yes | yes: 10 |
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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4I2M1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 9 |
GO:0004519 | endonuclease activity | 5 | 9 |
GO:0004521 | RNA endonuclease activity | 5 | 9 |
GO:0004525 | ribonuclease III activity | 6 | 9 |
GO:0004540 | RNA nuclease activity | 4 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 9 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 9 |
GO:0032296 | double-stranded RNA-specific ribonuclease activity | 5 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.418 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.467 |
DEG_APCC_DBOX_1 | 112 | 120 | PF00400 | 0.523 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.575 |
DEG_APCC_DBOX_1 | 64 | 72 | PF00400 | 0.447 |
DOC_CYCLIN_RxL_1 | 15 | 24 | PF00134 | 0.587 |
DOC_MAPK_gen_1 | 59 | 70 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 72 | 78 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 63 | 70 | PF00069 | 0.544 |
DOC_MAPK_NFAT4_5 | 63 | 71 | PF00069 | 0.530 |
DOC_PP2B_LxvP_1 | 201 | 204 | PF13499 | 0.509 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.631 |
DOC_PP4_FxxP_1 | 319 | 322 | PF00568 | 0.609 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.744 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.737 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 15 | 19 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 169 | 179 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 272 | 280 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 89 | 97 | PF00244 | 0.533 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.642 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.642 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.642 |
LIG_EH1_1 | 147 | 155 | PF00400 | 0.579 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.455 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.537 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.516 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.668 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.680 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.450 |
LIG_LIR_Apic_2 | 308 | 312 | PF02991 | 0.679 |
LIG_LIR_Gen_1 | 224 | 235 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.439 |
LIG_NRBOX | 17 | 23 | PF00104 | 0.542 |
LIG_NRBOX | 77 | 83 | PF00104 | 0.388 |
LIG_PCNA_yPIPBox_3 | 72 | 82 | PF02747 | 0.426 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.663 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 227 | 231 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.577 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.746 |
LIG_SH3_1 | 118 | 124 | PF00018 | 0.539 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.539 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.478 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.496 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.516 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.649 |
LIG_SUMO_SIM_anti_2 | 205 | 211 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.679 |
LIG_TYR_ITIM | 225 | 230 | PF00017 | 0.415 |
LIG_WRC_WIRS_1 | 306 | 311 | PF05994 | 0.676 |
MOD_CDK_SPK_2 | 252 | 257 | PF00069 | 0.750 |
MOD_CDK_SPxxK_3 | 162 | 169 | PF00069 | 0.679 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.593 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.554 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.568 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.647 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.482 |
MOD_DYRK1A_RPxSP_1 | 162 | 166 | PF00069 | 0.708 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.710 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.666 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.547 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.518 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.656 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.635 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.694 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.498 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.453 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.579 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.453 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.452 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.525 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.522 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.526 |
MOD_OFUCOSY | 299 | 305 | PF10250 | 0.528 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.632 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.641 |
MOD_PKA_1 | 59 | 65 | PF00069 | 0.540 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.495 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.614 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.655 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.710 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.482 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.737 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.746 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.576 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.441 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.665 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.633 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.684 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.506 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.758 |
MOD_SUMO_rev_2 | 231 | 240 | PF00179 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.410 |
TRG_NES_CRM1_1 | 231 | 244 | PF08389 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 19 | 24 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6V9 | Leptomonas seymouri | 58% | 86% |
A0A1X0P3V7 | Trypanosomatidae | 51% | 96% |
A0A1X0P4R2 | Trypanosomatidae | 23% | 91% |
A0A3Q8ID52 | Leishmania donovani | 99% | 100% |
A0A3R7MNH0 | Trypanosoma rangeli | 52% | 95% |
A4HFF2 | Leishmania braziliensis | 89% | 100% |
D0A5N3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 97% |
E9AD11 | Leishmania major | 97% | 100% |
E9AYT6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |