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:0000315 | organellar large ribosomal subunit | 5 | 1 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 1 |
GO:0015934 | large ribosomal subunit | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0044391 | ribosomal subunit | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8ID92
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 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:0000154 | rRNA modification | 6 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031167 | rRNA methylation | 5 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
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:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.733 |
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.723 |
CLV_MEL_PAP_1 | 65 | 71 | PF00089 | 0.494 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.426 |
CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.401 |
DEG_SPOP_SBC_1 | 104 | 108 | PF00917 | 0.527 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.737 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.612 |
DOC_CYCLIN_RxL_1 | 374 | 383 | PF00134 | 0.488 |
DOC_MAPK_gen_1 | 322 | 329 | PF00069 | 0.455 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.460 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.609 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.732 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.666 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 299 | 309 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.529 |
LIG_BIR_III_4 | 145 | 149 | PF00653 | 0.494 |
LIG_BIR_III_4 | 354 | 358 | PF00653 | 0.691 |
LIG_CtBP_PxDLS_1 | 265 | 269 | PF00389 | 0.527 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.483 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.388 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.417 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.687 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.521 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.554 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.465 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.472 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.498 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.487 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.748 |
LIG_LIR_Apic_2 | 235 | 239 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.396 |
LIG_Pex14_1 | 387 | 391 | PF04695 | 0.450 |
LIG_Rb_LxCxE_1 | 193 | 206 | PF01857 | 0.535 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.481 |
LIG_SH2_SRC | 237 | 240 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.467 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.449 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.703 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.688 |
LIG_SUMO_SIM_par_1 | 264 | 270 | PF11976 | 0.527 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.571 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.550 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.512 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.455 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.713 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.678 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.469 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.494 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.474 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.508 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.539 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.762 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.618 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.549 |
MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.323 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.671 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.414 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.308 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.611 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.480 |
MOD_GlcNHglycan | 354 | 358 | PF01048 | 0.691 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.479 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.460 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.543 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.716 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.650 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.492 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.436 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.607 |
MOD_NEK2_2 | 290 | 295 | PF00069 | 0.497 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.460 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.503 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.559 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.638 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.462 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.434 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.531 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.398 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.475 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.641 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.476 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.510 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.484 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.460 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.687 |
MOD_SUMO_rev_2 | 396 | 404 | PF00179 | 0.577 |
TRG_DiLeu_BaEn_1 | 85 | 90 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 374 | 379 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.252 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.249 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.249 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK00 | Leptomonas seymouri | 67% | 100% |
A0A0S4J448 | Bodo saltans | 41% | 100% |
A0A1X0NJV9 | Trypanosomatidae | 29% | 73% |
A0A1X0NRJ9 | Trypanosomatidae | 40% | 100% |
A0A3R7K4S3 | Trypanosoma rangeli | 47% | 100% |
A4HKN4 | Leishmania braziliensis | 80% | 100% |
A4I865 | Leishmania infantum | 100% | 100% |
D0AAD3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B323 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q0P5D8 | Bos taurus | 30% | 100% |
Q0V8R7 | Bos taurus | 28% | 100% |
Q4KMK0 | Danio rerio | 32% | 100% |
Q4Q532 | Leishmania major | 92% | 100% |
Q5M7E3 | Xenopus laevis | 30% | 100% |
Q66KI9 | Xenopus tropicalis | 29% | 100% |
Q8CCT7 | Mus musculus | 31% | 100% |
Q96CB9 | Homo sapiens | 27% | 100% |
Q9CZ57 | Mus musculus | 29% | 100% |
V5B8C1 | Trypanosoma cruzi | 44% | 100% |