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: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: A4HYR3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.576 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.480 |
DOC_CKS1_1 | 156 | 161 | PF01111 | 0.561 |
DOC_CKS1_1 | 291 | 296 | PF01111 | 0.495 |
DOC_CYCLIN_RxL_1 | 206 | 216 | PF00134 | 0.389 |
DOC_CYCLIN_RxL_1 | 368 | 376 | PF00134 | 0.346 |
DOC_CYCLIN_yCln2_LP_2 | 254 | 260 | PF00134 | 0.509 |
DOC_MAPK_DCC_7 | 177 | 187 | PF00069 | 0.496 |
DOC_MAPK_HePTP_8 | 390 | 402 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 393 | 402 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.704 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.525 |
DOC_PP4_FxxP_1 | 179 | 182 | PF00568 | 0.509 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.424 |
LIG_14-3-3_CanoR_1 | 169 | 179 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 246 | 254 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 320 | 325 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 377 | 382 | PF00244 | 0.425 |
LIG_FAT_LD_1 | 187 | 195 | PF03623 | 0.334 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.640 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.611 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.390 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.457 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.211 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.452 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.399 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.344 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.371 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.390 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.602 |
LIG_LIR_Gen_1 | 216 | 222 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 314 | 324 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 329 | 337 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.373 |
LIG_NRBOX | 262 | 268 | PF00104 | 0.420 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.383 |
LIG_NRBOX | 365 | 371 | PF00104 | 0.344 |
LIG_NRBOX | 72 | 78 | PF00104 | 0.468 |
LIG_PCNA_yPIPBox_3 | 360 | 374 | PF02747 | 0.367 |
LIG_Pex3_1 | 370 | 381 | PF04882 | 0.472 |
LIG_PTB_Apo_2 | 93 | 100 | PF02174 | 0.435 |
LIG_PTB_Phospho_1 | 93 | 99 | PF10480 | 0.428 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 117 | 121 | PF00017 | 0.435 |
LIG_SH2_SRC | 29 | 32 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.318 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.211 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 99 | 103 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 172 | 175 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.207 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.394 |
LIG_SH3_1 | 392 | 398 | PF00018 | 0.524 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.665 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.378 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.508 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.531 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.524 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.523 |
LIG_SUMO_SIM_anti_2 | 111 | 118 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 192 | 198 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 277 | 284 | PF11976 | 0.291 |
LIG_SUMO_SIM_anti_2 | 332 | 337 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 183 | 188 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 192 | 198 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 301 | 307 | PF11976 | 0.357 |
LIG_TRFH_1 | 218 | 222 | PF08558 | 0.469 |
LIG_TYR_ITSM | 226 | 233 | PF00017 | 0.474 |
LIG_UBA3_1 | 262 | 268 | PF00899 | 0.420 |
LIG_UBA3_1 | 333 | 340 | PF00899 | 0.465 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.476 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.457 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.446 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.487 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.347 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.407 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.673 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.390 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.485 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.413 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.492 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.516 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.459 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.420 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.352 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.403 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.366 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.553 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.420 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.449 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.354 |
MOD_NEK2_2 | 311 | 316 | PF00069 | 0.360 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.457 |
MOD_PK_1 | 320 | 326 | PF00069 | 0.449 |
MOD_PKA_1 | 345 | 351 | PF00069 | 0.488 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.336 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.455 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.522 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.421 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.350 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.568 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.524 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.448 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.455 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.547 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.331 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.467 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.360 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.379 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.608 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.379 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.484 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.427 |
TRG_DiLeu_BaEn_1 | 111 | 116 | PF01217 | 0.472 |
TRG_DiLeu_BaEn_1 | 278 | 283 | PF01217 | 0.292 |
TRG_DiLeu_BaEn_1 | 329 | 334 | PF01217 | 0.363 |
TRG_DiLeu_BaEn_2 | 88 | 94 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 207 | 212 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.257 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.362 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 210 | 214 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7Z9 | Leptomonas seymouri | 76% | 74% |
A0A1X0NWF6 | Trypanosomatidae | 54% | 76% |
A0A3Q8IBN5 | Leishmania donovani | 100% | 74% |
A0A3R7K7U1 | Trypanosoma rangeli | 54% | 79% |
C9ZI67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 77% |
E9AIA5 | Leishmania braziliensis | 91% | 100% |
E9AUJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QCZ2 | Leishmania major | 97% | 100% |
V5BQU6 | Trypanosoma cruzi | 56% | 81% |