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:0005737 | cytoplasm | 2 | 3 |
GO:0005739 | mitochondrion | 5 | 3 |
GO:0005743 | mitochondrial inner membrane | 5 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0019866 | organelle inner membrane | 4 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0031966 | mitochondrial membrane | 4 | 12 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9ADU9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0006811 | monoatomic ion transport | 4 | 3 |
GO:0006812 | monoatomic cation transport | 5 | 3 |
GO:0006816 | calcium ion transport | 7 | 3 |
GO:0006851 | mitochondrial calcium ion transmembrane transport | 4 | 3 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 2 |
GO:0009987 | cellular process | 1 | 3 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0030001 | metal ion transport | 6 | 3 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 3 |
GO:0042592 | homeostatic process | 3 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 2 |
GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 3 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0070588 | calcium ion transmembrane transport | 6 | 3 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 3 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 3 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 3 |
GO:0098771 | inorganic ion homeostasis | 6 | 2 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 3 |
GO:0005432 | calcium:sodium antiporter activity | 7 | 3 |
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 3 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
GO:0015081 | sodium ion transmembrane transporter activity | 6 | 3 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 3 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 3 |
GO:0015297 | antiporter activity | 5 | 3 |
GO:0015298 | obsolete solute:monoatomic cation antiporter activity | 5 | 3 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
GO:0015368 | calcium:monoatomic cation antiporter activity | 7 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 3 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 3 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 12 |
GO:0043022 | ribosome binding | 4 | 12 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0044877 | protein-containing complex binding | 2 | 12 |
GO:0046872 | metal ion binding | 4 | 3 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 3 |
GO:0140828 | metal cation:monoatomic cation antiporter activity | 6 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.381 |
CLV_C14_Caspase3-7 | 377 | 381 | PF00656 | 0.567 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.501 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 235 | 241 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.287 |
DEG_APCC_DBOX_1 | 324 | 332 | PF00400 | 0.393 |
DEG_APCC_DBOX_1 | 338 | 346 | PF00400 | 0.390 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.645 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.616 |
DOC_AGCK_PIF_2 | 442 | 447 | PF00069 | 0.467 |
DOC_CYCLIN_RxL_1 | 79 | 89 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.344 |
DOC_MAPK_gen_1 | 31 | 42 | PF00069 | 0.648 |
DOC_MAPK_gen_1 | 314 | 322 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 325 | 331 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 69 | 77 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 79 | 85 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 201 | 210 | PF00069 | 0.322 |
DOC_PP1_RVXF_1 | 53 | 59 | PF00149 | 0.554 |
DOC_PP1_RVXF_1 | 60 | 66 | PF00149 | 0.527 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.344 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.308 |
DOC_PP4_FxxP_1 | 200 | 203 | PF00568 | 0.381 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.431 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.711 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.668 |
DOC_USP7_UBL2_3 | 364 | 368 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 407 | 411 | PF12436 | 0.474 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.381 |
LIG_14-3-3_CanoR_1 | 274 | 282 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 33 | 50 | PF00022 | 0.661 |
LIG_Actin_WH2_2 | 56 | 74 | PF00022 | 0.562 |
LIG_APCC_ABBA_1 | 103 | 108 | PF00400 | 0.344 |
LIG_APCC_ABBAyCdc20_2 | 133 | 139 | PF00400 | 0.362 |
LIG_BRCT_BRCA1_1 | 438 | 442 | PF00533 | 0.358 |
LIG_Clathr_ClatBox_1 | 250 | 254 | PF01394 | 0.301 |
LIG_eIF4E_1 | 51 | 57 | PF01652 | 0.542 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.720 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.255 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.343 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.750 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.288 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.487 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.214 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.433 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.378 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.579 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.487 |
LIG_LIR_Apic_2 | 198 | 203 | PF02991 | 0.337 |
LIG_LIR_Apic_2 | 302 | 308 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 287 | 293 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 297 | 308 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 439 | 449 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.328 |
LIG_MYND_1 | 119 | 123 | PF01753 | 0.276 |
LIG_NRP_CendR_1 | 500 | 501 | PF00754 | 0.808 |
LIG_PCNA_PIPBox_1 | 389 | 398 | PF02747 | 0.389 |
LIG_PCNA_yPIPBox_3 | 389 | 403 | PF02747 | 0.392 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.554 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.318 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.534 |
LIG_SH2_STAT3 | 67 | 70 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.372 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.362 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.505 |
LIG_Sin3_3 | 107 | 114 | PF02671 | 0.363 |
LIG_TRAF2_1 | 478 | 481 | PF00917 | 0.623 |
LIG_TRAF2_1 | 487 | 490 | PF00917 | 0.588 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.276 |
LIG_TYR_ITIM | 42 | 47 | PF00017 | 0.642 |
LIG_UBA3_1 | 404 | 412 | PF00899 | 0.388 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.287 |
MOD_CDK_SPxxK_3 | 227 | 234 | PF00069 | 0.381 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.704 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.496 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.544 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.559 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.276 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.440 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.499 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.590 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.487 |
MOD_Cter_Amidation | 498 | 501 | PF01082 | 0.799 |
MOD_DYRK1A_RPxSP_1 | 227 | 231 | PF00069 | 0.381 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.531 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.545 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.724 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.642 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.270 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.705 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.300 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.368 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.380 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.470 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.495 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.402 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.381 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.261 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.557 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.545 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.648 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.290 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.330 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.628 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.281 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.351 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.558 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.487 |
MOD_NEK2_2 | 140 | 145 | PF00069 | 0.301 |
MOD_NEK2_2 | 278 | 283 | PF00069 | 0.340 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.277 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.734 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.628 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.374 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.287 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.383 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.473 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.325 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.411 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.336 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.555 |
MOD_Plk_2-3 | 489 | 495 | PF00069 | 0.608 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.678 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.311 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.276 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.473 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.377 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.381 |
MOD_SUMO_rev_2 | 485 | 493 | PF00179 | 0.591 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 79 | 84 | PF01217 | 0.501 |
TRG_DiLeu_LyEn_5 | 246 | 251 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.702 |
TRG_NLS_MonoExtC_3 | 409 | 414 | PF00514 | 0.523 |
TRG_NLS_MonoExtN_4 | 407 | 414 | PF00514 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 411 | 415 | PF00026 | 0.729 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD73 | Leptomonas seymouri | 85% | 99% |
A0A0S4JFV9 | Bodo saltans | 52% | 100% |
A0A1X0NZY3 | Trypanosomatidae | 62% | 100% |
A0A3S5IR30 | Trypanosoma rangeli | 65% | 100% |
A0A3S7X2D5 | Leishmania donovani | 99% | 100% |
A4HHA3 | Leishmania braziliensis | 94% | 99% |
A4I4E9 | Leishmania infantum | 99% | 100% |
C9ZLK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9ALY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
V5DI32 | Trypanosoma cruzi | 64% | 100% |