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:0000428 | DNA-directed RNA polymerase complex | 4 | 11 |
GO:0005666 | RNA polymerase III complex | 4 | 11 |
GO:0030880 | RNA polymerase complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0055029 | nuclear DNA-directed RNA polymerase complex | 3 | 11 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 11 |
GO:0140513 | nuclear protein-containing complex | 2 | 11 |
GO:0140535 | intracellular protein-containing complex | 2 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:1990234 | transferase complex | 3 | 11 |
Related structures:
AlphaFold database: A4HHE3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006351 | DNA-templated transcription | 7 | 11 |
GO:0006383 | transcription by RNA polymerase III | 8 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0032774 | RNA biosynthetic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:0097659 | nucleic acid-templated transcription | 6 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003899 | DNA-directed 5'-3' RNA polymerase activity | 6 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0034062 | 5'-3' RNA polymerase activity | 5 | 1 |
GO:0097747 | RNA polymerase activity | 4 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.454 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.355 |
CLV_PCSK_FUR_1 | 131 | 135 | PF00082 | 0.335 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.441 |
CLV_PCSK_FUR_1 | 55 | 59 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.441 |
CLV_PCSK_PC7_1 | 53 | 59 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.354 |
DEG_MDM2_SWIB_1 | 162 | 170 | PF02201 | 0.447 |
DEG_SCF_FBW7_1 | 348 | 355 | PF00400 | 0.227 |
DEG_SPOP_SBC_1 | 251 | 255 | PF00917 | 0.448 |
DOC_CKS1_1 | 205 | 210 | PF01111 | 0.227 |
DOC_CKS1_1 | 293 | 298 | PF01111 | 0.480 |
DOC_CYCLIN_RxL_1 | 29 | 39 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 389 | 395 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 29 | 36 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 333 | 342 | PF00069 | 0.383 |
DOC_MAPK_HePTP_8 | 259 | 271 | PF00069 | 0.227 |
DOC_MAPK_HePTP_8 | 54 | 70 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 262 | 271 | PF00069 | 0.227 |
DOC_MAPK_MEF2A_6 | 335 | 344 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 10 | 17 | PF00149 | 0.227 |
DOC_PP1_RVXF_1 | 176 | 183 | PF00149 | 0.447 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.465 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.447 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.227 |
LIG_14-3-3_CanoR_1 | 103 | 113 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 134 | 139 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 172 | 180 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 320 | 329 | PF00244 | 0.321 |
LIG_Actin_WH2_2 | 41 | 59 | PF00022 | 0.335 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.587 |
LIG_Clathr_ClatBox_1 | 138 | 142 | PF01394 | 0.335 |
LIG_deltaCOP1_diTrp_1 | 164 | 173 | PF00928 | 0.447 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.474 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.412 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.341 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.272 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.255 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.443 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.428 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.383 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.447 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.432 |
LIG_GBD_Chelix_1 | 70 | 78 | PF00786 | 0.447 |
LIG_LIR_Gen_1 | 181 | 189 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 405 | 415 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 64 | 74 | PF02991 | 0.359 |
LIG_LIR_LC3C_4 | 207 | 212 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.359 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.442 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.227 |
LIG_SH2_PTP2 | 67 | 70 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.319 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.368 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.411 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.266 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.378 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.192 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.335 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.355 |
LIG_SUMO_SIM_anti_2 | 76 | 83 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.335 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.237 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.227 |
LIG_TYR_ITIM | 25 | 30 | PF00017 | 0.447 |
LIG_WRC_WIRS_1 | 179 | 184 | PF05994 | 0.480 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.227 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.422 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.397 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.224 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.480 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.330 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.344 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.292 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.402 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.454 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.482 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.370 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.418 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.349 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.314 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.370 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.370 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.274 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.488 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.233 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.447 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.335 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.335 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.480 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.322 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.403 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.339 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.233 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.394 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.437 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.415 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.442 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.317 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.393 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.447 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.408 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.250 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.335 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.348 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.480 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.413 |
MOD_NEK2_2 | 426 | 431 | PF00069 | 0.482 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.480 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.424 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.398 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.480 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.447 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.322 |
MOD_PKB_1 | 318 | 326 | PF00069 | 0.442 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.480 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.441 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.287 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.402 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.304 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.480 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.447 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.428 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.364 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.444 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.438 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.227 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.335 |
MOD_SUMO_for_1 | 30 | 33 | PF00179 | 0.447 |
TRG_DiLeu_BaEn_1 | 76 | 81 | PF01217 | 0.335 |
TRG_DiLeu_BaEn_2 | 168 | 174 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 418 | 423 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.364 |
TRG_NES_CRM1_1 | 268 | 279 | PF08389 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILC6 | Leptomonas seymouri | 65% | 100% |
A0A1X0NZS8 | Trypanosomatidae | 42% | 100% |
A0A3Q8IBH1 | Leishmania donovani | 86% | 100% |
A0A3R7NQJ5 | Trypanosoma rangeli | 40% | 100% |
A4I4I9 | Leishmania infantum | 87% | 100% |
C9ZL77 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9ADZ0 | Leishmania major | 86% | 100% |
E9ALU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5B1R1 | Trypanosoma cruzi | 39% | 100% |