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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IAX5
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 1 |
GO:0001510 | RNA methylation | 4 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031167 | rRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000179 | rRNA (adenine-N6,N6-)-dimethyltransferase activity | 6 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008170 | N-methyltransferase activity | 5 | 11 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008649 | rRNA methyltransferase activity | 5 | 11 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 11 |
GO:0016433 | rRNA (adenine) methyltransferase activity | 6 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 106 | 112 | PF00089 | 0.194 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.537 |
CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.249 |
DEG_ODPH_VHL_1 | 308 | 321 | PF01847 | 0.453 |
DOC_ANK_TNKS_1 | 225 | 232 | PF00023 | 0.551 |
DOC_ANK_TNKS_1 | 27 | 34 | PF00023 | 0.392 |
DOC_ANK_TNKS_1 | 342 | 349 | PF00023 | 0.535 |
DOC_CKS1_1 | 72 | 77 | PF01111 | 0.497 |
DOC_CYCLIN_RxL_1 | 88 | 95 | PF00134 | 0.440 |
DOC_MAPK_MEF2A_6 | 52 | 59 | PF00069 | 0.440 |
DOC_MAPK_NFAT4_5 | 52 | 60 | PF00069 | 0.440 |
DOC_PP1_RVXF_1 | 178 | 184 | PF00149 | 0.600 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.694 |
DOC_USP7_UBL2_3 | 35 | 39 | PF12436 | 0.375 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 172 | 181 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 318 | 322 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 382 | 387 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.440 |
LIG_Actin_WH2_2 | 128 | 144 | PF00022 | 0.475 |
LIG_Actin_WH2_2 | 368 | 384 | PF00022 | 0.492 |
LIG_APCC_ABBA_1 | 110 | 115 | PF00400 | 0.535 |
LIG_BIR_III_4 | 191 | 195 | PF00653 | 0.593 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.440 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.556 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.450 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.458 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.470 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.445 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.598 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.425 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.440 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.440 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.440 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.535 |
LIG_LIR_Gen_1 | 122 | 133 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.440 |
LIG_PTB_Apo_2 | 261 | 268 | PF02174 | 0.440 |
LIG_REV1ctd_RIR_1 | 324 | 334 | PF16727 | 0.492 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.504 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.649 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 401 | 404 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.535 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.603 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.553 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.434 |
LIG_SUMO_SIM_anti_2 | 136 | 143 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 317 | 323 | PF11976 | 0.440 |
LIG_SUMO_SIM_anti_2 | 416 | 421 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 349 | 354 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 413 | 418 | PF11976 | 0.453 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.656 |
LIG_TRAF2_2 | 217 | 222 | PF00917 | 0.547 |
LIG_UBA3_1 | 54 | 58 | PF00899 | 0.440 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.497 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.394 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.699 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.789 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.440 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.665 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.458 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.440 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.470 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.471 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.458 |
MOD_DYRK1A_RPxSP_1 | 155 | 159 | PF00069 | 0.537 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.543 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.684 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.688 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.584 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.659 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.688 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.586 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.440 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.525 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.440 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.456 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.585 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.527 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.477 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.568 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.522 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.470 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.350 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.440 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.752 |
MOD_PIKK_1 | 279 | 285 | PF00454 | 0.535 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.365 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.414 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.635 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.770 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.440 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.440 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.440 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.448 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.535 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.446 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.512 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.470 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.440 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.535 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.394 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.576 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.680 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.690 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.578 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.514 |
MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.440 |
MOD_SUMO_for_1 | 29 | 32 | PF00179 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.567 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.443 |
TRG_NES_CRM1_1 | 397 | 409 | PF08389 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXZ3 | Leptomonas seymouri | 78% | 86% |
A0A1X0NJH8 | Trypanosomatidae | 56% | 87% |
A0A3R7NNC2 | Trypanosoma rangeli | 58% | 96% |
A0A3S7X8W9 | Leishmania donovani | 100% | 100% |
A4HMA9 | Leishmania braziliensis | 88% | 100% |
D0A280 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 99% |
E9AEQ2 | Leishmania major | 94% | 100% |
E9B5V7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BN79 | Trypanosoma cruzi | 61% | 97% |