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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: Q4QAW9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006370 | 7-methylguanosine mRNA capping | 8 | 13 |
GO:0006396 | RNA processing | 6 | 13 |
GO:0006397 | mRNA processing | 7 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009452 | 7-methylguanosine RNA capping | 8 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016070 | RNA metabolic process | 5 | 13 |
GO:0016071 | mRNA metabolic process | 6 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0036260 | RNA capping | 7 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003746 | translation elongation factor activity | 4 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004483 | mRNA (nucleoside-2'-O-)-methyltransferase activity | 6 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0008135 | translation factor activity, RNA binding | 3 | 13 |
GO:0008168 | methyltransferase activity | 4 | 13 |
GO:0008171 | O-methyltransferase activity | 5 | 13 |
GO:0008173 | RNA methyltransferase activity | 4 | 13 |
GO:0008174 | mRNA methyltransferase activity | 5 | 13 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 13 |
GO:0045182 | translation regulator activity | 1 | 13 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 216 | 220 | PF00656 | 0.395 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.141 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.458 |
CLV_PCSK_FUR_1 | 132 | 136 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 244 | 246 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.696 |
CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.437 |
CLV_PCSK_PC7_1 | 402 | 408 | PF00082 | 0.375 |
CLV_PCSK_PC7_1 | 412 | 418 | PF00082 | 0.616 |
CLV_PCSK_PC7_1 | 422 | 428 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.331 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.539 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.336 |
DOC_CYCLIN_yCln2_LP_2 | 312 | 318 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.425 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.204 |
DOC_MAPK_MEF2A_6 | 230 | 239 | PF00069 | 0.330 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.450 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.323 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.560 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.557 |
DOC_WD40_RPTOR_TOS_1 | 179 | 184 | PF00400 | 0.439 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 132 | 138 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 253 | 259 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 326 | 331 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.432 |
LIG_14-3-3_CterR_2 | 433 | 438 | PF00244 | 0.514 |
LIG_CaM_NSCaTE_8 | 327 | 334 | PF13499 | 0.386 |
LIG_deltaCOP1_diTrp_1 | 176 | 179 | PF00928 | 0.427 |
LIG_eIF4E_1 | 37 | 43 | PF01652 | 0.348 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.348 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.292 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.336 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.418 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.468 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.452 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.396 |
LIG_KLC1_Yacidic_2 | 214 | 219 | PF13176 | 0.472 |
LIG_LIR_Apic_2 | 24 | 30 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 391 | 400 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 93 | 102 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 93 | 97 | PF02991 | 0.367 |
LIG_PCNA_TLS_4 | 280 | 287 | PF02747 | 0.488 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.493 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.519 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.492 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.404 |
LIG_SH2_GRB2like | 18 | 21 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.546 |
LIG_SH2_SRC | 217 | 220 | PF00017 | 0.446 |
LIG_SH2_STAT3 | 205 | 208 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.487 |
LIG_SH3_1 | 189 | 195 | PF00018 | 0.336 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.584 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.336 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.346 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.313 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.416 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.277 |
LIG_SUMO_SIM_par_1 | 115 | 123 | PF11976 | 0.355 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.472 |
LIG_TRFH_1 | 86 | 90 | PF08558 | 0.418 |
LIG_TYR_ITIM | 340 | 345 | PF00017 | 0.538 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.509 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.450 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.445 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.214 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.394 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.336 |
MOD_Cter_Amidation | 420 | 423 | PF01082 | 0.734 |
MOD_Cter_Amidation | 429 | 432 | PF01082 | 0.776 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.323 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.473 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.415 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.464 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.371 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.262 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.377 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.432 |
MOD_LATS_1 | 324 | 330 | PF00433 | 0.474 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.643 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.438 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.396 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.448 |
MOD_NEK2_2 | 254 | 259 | PF00069 | 0.417 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.472 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.719 |
MOD_PKA_1 | 59 | 65 | PF00069 | 0.316 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.376 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.434 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.472 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.485 |
MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.472 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.450 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.394 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.495 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.394 |
TRG_DiLeu_BaEn_4 | 213 | 219 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 277 | 282 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.537 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.771 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.453 |
TRG_NLS_Bipartite_1 | 40 | 62 | PF00514 | 0.421 |
TRG_NLS_Bipartite_1 | 416 | 435 | PF00514 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.398 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HV56 | Leptomonas seymouri | 68% | 100% |
A0A0S4J219 | Bodo saltans | 49% | 100% |
A0A1X0NIX1 | Trypanosomatidae | 50% | 100% |
A0A3S7WY48 | Leishmania donovani | 91% | 100% |
A0A422P442 | Trypanosoma rangeli | 52% | 100% |
A4HD69 | Leishmania braziliensis | 82% | 100% |
C9ZZ04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 86% |
D0A6Y2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AH23 | Leishmania infantum | 92% | 100% |
E9AWK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BRC4 | Trypanosoma cruzi | 51% | 100% |