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: 11 |
NetGPI | no | yes: 0, no: 11 |
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: A4HMA9
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 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008649 | rRNA methyltransferase activity | 5 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016433 | rRNA (adenine) methyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 449 | 453 | PF00656 | 0.522 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.507 |
CLV_PCSK_FUR_1 | 212 | 216 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.243 |
CLV_Separin_Metazoa | 141 | 145 | PF03568 | 0.274 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.474 |
DEG_ODPH_VHL_1 | 310 | 323 | PF01847 | 0.460 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.616 |
DOC_ANK_TNKS_1 | 29 | 36 | PF00023 | 0.421 |
DOC_ANK_TNKS_1 | 344 | 351 | PF00023 | 0.538 |
DOC_CKS1_1 | 74 | 79 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 90 | 97 | PF00134 | 0.436 |
DOC_MAPK_MEF2A_6 | 54 | 61 | PF00069 | 0.436 |
DOC_MAPK_NFAT4_5 | 54 | 62 | PF00069 | 0.436 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.400 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.519 |
LIG_14-3-3_CanoR_1 | 30 | 36 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 320 | 324 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 384 | 389 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 426 | 431 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 71 | 77 | PF00244 | 0.446 |
LIG_Actin_WH2_2 | 130 | 146 | PF00022 | 0.470 |
LIG_Actin_WH2_2 | 370 | 386 | PF00022 | 0.488 |
LIG_APCC_ABBA_1 | 112 | 117 | PF00400 | 0.538 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.446 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.558 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.444 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.464 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.465 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.440 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.436 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.436 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.446 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.639 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.504 |
LIG_LIR_Gen_1 | 315 | 324 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 429 | 437 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.295 |
LIG_PDZ_Class_1 | 464 | 469 | PF00595 | 0.488 |
LIG_PTB_Apo_2 | 121 | 128 | PF02174 | 0.547 |
LIG_PTB_Apo_2 | 241 | 248 | PF02174 | 0.553 |
LIG_PTB_Apo_2 | 263 | 270 | PF02174 | 0.436 |
LIG_REV1ctd_RIR_1 | 326 | 336 | PF16727 | 0.538 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.537 |
LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 51 | 55 | PF00017 | 0.446 |
LIG_SH2_STAT3 | 122 | 125 | PF00017 | 0.487 |
LIG_SH2_STAT3 | 403 | 406 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.538 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.606 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.607 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.480 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.547 |
LIG_SUMO_SIM_anti_2 | 138 | 145 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 418 | 423 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 351 | 356 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 415 | 420 | PF11976 | 0.460 |
LIG_TRAF2_2 | 442 | 447 | PF00917 | 0.589 |
LIG_UBA3_1 | 56 | 60 | PF00899 | 0.436 |
MOD_CDK_SPxK_1 | 73 | 79 | PF00069 | 0.503 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.748 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.436 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.634 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.465 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.436 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.468 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.453 |
MOD_DYRK1A_RPxSP_1 | 157 | 161 | PF00069 | 0.600 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.572 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.682 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.614 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.661 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.589 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.651 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.436 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.530 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.479 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.446 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.463 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.320 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.493 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.573 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.483 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.564 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.506 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.465 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.345 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.436 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.755 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.457 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.449 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.442 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.446 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.460 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.436 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.520 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.510 |
MOD_Plk_2-3 | 446 | 452 | PF00069 | 0.521 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.441 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.507 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.464 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.448 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.469 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.538 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.699 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.703 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.519 |
MOD_SUMO_for_1 | 259 | 262 | PF00179 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.660 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.520 |
TRG_NES_CRM1_1 | 399 | 411 | PF08389 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 209 | 213 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.252 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXZ3 | Leptomonas seymouri | 78% | 87% |
A0A0S4IZP9 | Bodo saltans | 48% | 88% |
A0A1X0NJH8 | Trypanosomatidae | 54% | 88% |
A0A3R7NNC2 | Trypanosoma rangeli | 60% | 98% |
A0A3S7X8W9 | Leishmania donovani | 88% | 100% |
A4IAX5 | Leishmania infantum | 88% | 100% |
D0A280 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AEQ2 | Leishmania major | 88% | 100% |
E9B5V7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BN79 | Trypanosoma cruzi | 61% | 98% |