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 | 2 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 2 |
GO:0015934 | large ribosomal subunit | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0044391 | ribosomal subunit | 3 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q532
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 2 |
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
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:0016072 | rRNA metabolic process | 7 | 2 |
GO:0031167 | rRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 12 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
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 |
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 | 0.491 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.733 |
CLV_MEL_PAP_1 | 65 | 71 | PF00089 | 0.496 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.479 |
CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.420 |
DEG_SPOP_SBC_1 | 405 | 409 | PF00917 | 0.744 |
DOC_CKS1_1 | 364 | 369 | PF01111 | 0.548 |
DOC_CYCLIN_RxL_1 | 375 | 384 | PF00134 | 0.490 |
DOC_MAPK_gen_1 | 322 | 329 | PF00069 | 0.456 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.462 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.511 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.742 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.507 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.656 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 299 | 309 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.525 |
LIG_BIR_III_4 | 145 | 149 | PF00653 | 0.494 |
LIG_BIR_III_4 | 355 | 359 | PF00653 | 0.686 |
LIG_CtBP_PxDLS_1 | 265 | 269 | PF00389 | 0.528 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.548 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.678 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.494 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.503 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.354 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.601 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.509 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.555 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.491 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.479 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.516 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.479 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.749 |
LIG_LIR_Apic_2 | 235 | 239 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.397 |
LIG_Pex14_1 | 388 | 392 | PF04695 | 0.454 |
LIG_Rb_LxCxE_1 | 193 | 206 | PF01857 | 0.536 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.484 |
LIG_SH2_SRC | 237 | 240 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.477 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.450 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.716 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.647 |
LIG_SUMO_SIM_par_1 | 264 | 270 | PF11976 | 0.528 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.575 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.551 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.517 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.461 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.707 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.675 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.463 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.495 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.475 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.528 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.532 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.755 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.605 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.546 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.410 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.301 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.754 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.480 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.450 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.543 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.350 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.708 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.667 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.503 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.437 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.612 |
MOD_NEK2_2 | 290 | 295 | PF00069 | 0.482 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.461 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.506 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.476 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.560 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.454 |
MOD_PKB_1 | 9 | 17 | PF00069 | 0.707 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.454 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.435 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.536 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.429 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.479 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.589 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.486 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.511 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.485 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.461 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.626 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 114 | 120 | PF00179 | 0.515 |
MOD_SUMO_rev_2 | 397 | 405 | PF00179 | 0.579 |
TRG_DiLeu_BaEn_1 | 85 | 90 | PF01217 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 375 | 380 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.253 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.250 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.250 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 378 | 383 | PF00026 | 0.421 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK00 | Leptomonas seymouri | 67% | 100% |
A0A0S4J448 | Bodo saltans | 40% | 100% |
A0A1X0NJV9 | Trypanosomatidae | 29% | 73% |
A0A1X0NRJ9 | Trypanosomatidae | 41% | 100% |
A0A3Q8ID92 | Leishmania donovani | 92% | 100% |
A0A3R7K4S3 | Trypanosoma rangeli | 47% | 100% |
A4HKN4 | Leishmania braziliensis | 80% | 98% |
A4I865 | Leishmania infantum | 92% | 100% |
D0AAD3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B323 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q0P5D8 | Bos taurus | 29% | 100% |
Q0V8R7 | Bos taurus | 31% | 100% |
Q4KMK0 | Danio rerio | 31% | 100% |
Q5M7E3 | Xenopus laevis | 29% | 100% |
Q66KI9 | Xenopus tropicalis | 29% | 100% |
Q8CCT7 | Mus musculus | 29% | 100% |
Q96CB9 | Homo sapiens | 26% | 100% |
Q9CZ57 | Mus musculus | 26% | 100% |
V5B8C1 | Trypanosoma cruzi | 43% | 100% |