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: E9B5V7
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_NRD_NRD_1 | 155 | 157 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.478 |
CLV_PCSK_FUR_1 | 211 | 215 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.219 |
DEG_ODPH_VHL_1 | 309 | 322 | PF01847 | 0.436 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.604 |
DOC_ANK_TNKS_1 | 28 | 35 | PF00023 | 0.384 |
DOC_ANK_TNKS_1 | 343 | 350 | PF00023 | 0.514 |
DOC_CKS1_1 | 73 | 78 | PF01111 | 0.478 |
DOC_CYCLIN_RxL_1 | 89 | 96 | PF00134 | 0.411 |
DOC_MAPK_MEF2A_6 | 53 | 60 | PF00069 | 0.411 |
DOC_MAPK_NFAT4_5 | 53 | 61 | PF00069 | 0.411 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.368 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 214 | 220 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 319 | 323 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 383 | 388 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 70 | 76 | PF00244 | 0.422 |
LIG_Actin_WH2_2 | 369 | 385 | PF00022 | 0.463 |
LIG_APCC_ABBA_1 | 111 | 116 | PF00400 | 0.514 |
LIG_BIR_III_4 | 192 | 196 | PF00653 | 0.586 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.422 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.533 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.419 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.440 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.441 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.415 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.405 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.411 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.411 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.422 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.480 |
LIG_LIR_Gen_1 | 314 | 323 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.411 |
LIG_PTB_Apo_2 | 120 | 127 | PF02174 | 0.523 |
LIG_PTB_Apo_2 | 140 | 147 | PF02174 | 0.222 |
LIG_PTB_Apo_2 | 240 | 247 | PF02174 | 0.538 |
LIG_PTB_Apo_2 | 262 | 269 | PF02174 | 0.411 |
LIG_REV1ctd_RIR_1 | 325 | 335 | PF16727 | 0.514 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.496 |
LIG_SH2_GRB2like | 121 | 124 | PF00017 | 0.496 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.687 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 402 | 405 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.514 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.600 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.508 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.432 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 137 | 144 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 318 | 324 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 417 | 422 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 350 | 355 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 414 | 419 | PF11976 | 0.436 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.667 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.493 |
LIG_TRAF2_2 | 441 | 446 | PF00917 | 0.548 |
LIG_UBA3_1 | 55 | 59 | PF00899 | 0.411 |
MOD_CDK_SPxK_1 | 72 | 78 | PF00069 | 0.478 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.772 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.411 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.634 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.441 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.411 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.451 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.444 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.429 |
MOD_DYRK1A_RPxSP_1 | 156 | 160 | PF00069 | 0.553 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.545 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.657 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.655 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.573 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.651 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.592 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.725 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.411 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.505 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.422 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.439 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.296 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.463 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.552 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.459 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.539 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.482 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.441 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.321 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.411 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.514 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.338 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.420 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.621 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.418 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.422 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.411 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.496 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.486 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.417 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.483 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.440 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.424 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.514 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.652 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.684 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.680 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.529 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.495 |
MOD_SUMO_for_1 | 258 | 261 | PF00179 | 0.411 |
MOD_SUMO_for_1 | 30 | 33 | PF00179 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.602 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.442 |
TRG_NES_CRM1_1 | 398 | 410 | PF08389 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.228 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXZ3 | Leptomonas seymouri | 79% | 86% |
A0A0S4IZP9 | Bodo saltans | 46% | 87% |
A0A1X0NJH8 | Trypanosomatidae | 56% | 87% |
A0A3R7NNC2 | Trypanosoma rangeli | 58% | 97% |
A0A3S7X8W9 | Leishmania donovani | 93% | 100% |
A4HMA9 | Leishmania braziliensis | 88% | 100% |
A4IAX5 | Leishmania infantum | 92% | 100% |
D0A280 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 99% |
E9AEQ2 | Leishmania major | 94% | 100% |
Q121Q5 | Polaromonas sp. (strain JS666 / ATCC BAA-500) | 24% | 100% |
V5BN79 | Trypanosoma cruzi | 61% | 97% |