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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B6D4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.790 |
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.439 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.750 |
CLV_PCSK_FUR_1 | 361 | 365 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 141 | 143 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.204 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.233 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.488 |
CLV_PCSK_PC7_1 | 137 | 143 | PF00082 | 0.470 |
CLV_PCSK_PC7_1 | 360 | 366 | PF00082 | 0.570 |
CLV_PCSK_PC7_1 | 443 | 449 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.603 |
CLV_Separin_Metazoa | 91 | 95 | PF03568 | 0.604 |
DEG_SPOP_SBC_1 | 95 | 99 | PF00917 | 0.641 |
DOC_ANK_TNKS_1 | 381 | 388 | PF00023 | 0.545 |
DOC_ANK_TNKS_1 | 427 | 434 | PF00023 | 0.523 |
DOC_MAPK_gen_1 | 48 | 57 | PF00069 | 0.428 |
DOC_PP1_RVXF_1 | 432 | 438 | PF00149 | 0.601 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.390 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.578 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.510 |
DOC_USP7_UBL2_3 | 110 | 114 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.488 |
DOC_USP7_UBL2_3 | 219 | 223 | PF12436 | 0.495 |
DOC_USP7_UBL2_3 | 354 | 358 | PF12436 | 0.528 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.614 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.531 |
LIG_BIR_III_4 | 103 | 107 | PF00653 | 0.535 |
LIG_BIR_III_4 | 70 | 74 | PF00653 | 0.433 |
LIG_deltaCOP1_diTrp_1 | 283 | 290 | PF00928 | 0.402 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.465 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.245 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.399 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.556 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.588 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.337 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.415 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.449 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.443 |
LIG_Integrin_isoDGR_2 | 338 | 340 | PF01839 | 0.215 |
LIG_Integrin_RGD_1 | 333 | 335 | PF01839 | 0.249 |
LIG_LIR_Apic_2 | 398 | 403 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 227 | 235 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 284 | 295 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 394 | 403 | PF02991 | 0.693 |
LIG_LIR_LC3C_4 | 251 | 256 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.504 |
LIG_Pex14_2 | 118 | 122 | PF04695 | 0.629 |
LIG_PTB_Apo_2 | 273 | 280 | PF02174 | 0.402 |
LIG_PTB_Phospho_1 | 273 | 279 | PF10480 | 0.402 |
LIG_SH2_GRB2like | 397 | 400 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.402 |
LIG_SH3_2 | 442 | 447 | PF14604 | 0.571 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.554 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.570 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.561 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.473 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.402 |
LIG_UBA3_1 | 51 | 58 | PF00899 | 0.609 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.411 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.519 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.469 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.575 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.570 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.758 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.555 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.559 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.565 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.459 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.402 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.452 |
MOD_Cter_Amidation | 74 | 77 | PF01082 | 0.772 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.592 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.294 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.362 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.359 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.770 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.447 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.541 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.689 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.507 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.511 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.671 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.548 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.649 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.211 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.583 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.447 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.592 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.629 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.385 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.377 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.631 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.467 |
MOD_NEK2_2 | 268 | 273 | PF00069 | 0.324 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.467 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.613 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.502 |
MOD_PKA_1 | 41 | 47 | PF00069 | 0.464 |
MOD_PKA_1 | 447 | 453 | PF00069 | 0.517 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.402 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.535 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.517 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.721 |
MOD_PKB_1 | 138 | 146 | PF00069 | 0.604 |
MOD_PKB_1 | 378 | 386 | PF00069 | 0.571 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.326 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.517 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.325 |
MOD_SUMO_rev_2 | 119 | 127 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 217 | 225 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 292 | 301 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 306 | 315 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 350 | 356 | PF00179 | 0.636 |
MOD_SUMO_rev_2 | 376 | 381 | PF00179 | 0.662 |
MOD_SUMO_rev_2 | 426 | 435 | PF00179 | 0.542 |
MOD_SUMO_rev_2 | 54 | 60 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 62 | 71 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_2 | 268 | 274 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.577 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.598 |
TRG_NLS_Bipartite_1 | 363 | 383 | PF00514 | 0.644 |
TRG_NLS_MonoCore_2 | 400 | 405 | PF00514 | 0.679 |
TRG_NLS_MonoExtC_3 | 139 | 144 | PF00514 | 0.477 |
TRG_NLS_MonoExtC_3 | 400 | 406 | PF00514 | 0.594 |
TRG_NLS_MonoExtC_3 | 446 | 451 | PF00514 | 0.544 |
TRG_NLS_MonoExtN_4 | 137 | 144 | PF00514 | 0.537 |
TRG_NLS_MonoExtN_4 | 378 | 383 | PF00514 | 0.600 |
TRG_NLS_MonoExtN_4 | 445 | 452 | PF00514 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 212 | 217 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8R8 | Leptomonas seymouri | 72% | 100% |
A0A1X0P6L1 | Trypanosomatidae | 46% | 100% |
A0A3Q8IPK7 | Leishmania donovani | 92% | 100% |
A0A3R7LUT6 | Trypanosoma rangeli | 47% | 100% |
A4HMS6 | Leishmania braziliensis | 86% | 100% |
C9ZZA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AF78 | Leishmania major | 92% | 100% |
Q5M9F1 | Rattus norvegicus | 29% | 100% |
V5BNV3 | Trypanosoma cruzi | 48% | 100% |