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: 5 |
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:0005773 | vacuole | 5 | 13 |
GO:0016020 | membrane | 2 | 13 |
GO:0043226 | organelle | 2 | 13 |
GO:0043227 | membrane-bounded organelle | 3 | 13 |
GO:0043229 | intracellular organelle | 3 | 13 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: Q4QBZ3
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
GO:0006885 | regulation of pH | 8 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
GO:0030004 | obsolete cellular monovalent inorganic cation homeostasis | 6 | 2 |
GO:0030641 | regulation of cellular pH | 7 | 2 |
GO:0042592 | homeostatic process | 3 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
GO:0051453 | regulation of intracellular pH | 8 | 2 |
GO:0055067 | obsolete monovalent inorganic cation homeostasis | 7 | 2 |
GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.313 |
CLV_C14_Caspase3-7 | 586 | 590 | PF00656 | 0.520 |
CLV_MEL_PAP_1 | 129 | 135 | PF00089 | 0.292 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.378 |
CLV_PCSK_FUR_1 | 54 | 58 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 56 | 58 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.331 |
DEG_APCC_DBOX_1 | 426 | 434 | PF00400 | 0.420 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.683 |
DOC_CKS1_1 | 235 | 240 | PF01111 | 0.403 |
DOC_CYCLIN_yCln2_LP_2 | 390 | 396 | PF00134 | 0.325 |
DOC_MAPK_gen_1 | 466 | 474 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 605 | 612 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 358 | 366 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 427 | 435 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 466 | 474 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 72 | 79 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 310 | 317 | PF00149 | 0.518 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.325 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.361 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.318 |
DOC_USP7_UBL2_3 | 462 | 466 | PF12436 | 0.254 |
DOC_USP7_UBL2_3 | 551 | 555 | PF12436 | 0.683 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.249 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.455 |
LIG_Actin_WH2_2 | 622 | 639 | PF00022 | 0.406 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.285 |
LIG_deltaCOP1_diTrp_1 | 399 | 407 | PF00928 | 0.272 |
LIG_eIF4E_1 | 102 | 108 | PF01652 | 0.292 |
LIG_eIF4E_1 | 419 | 425 | PF01652 | 0.290 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.577 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.302 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.325 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.363 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.521 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.618 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.406 |
LIG_GBD_Chelix_1 | 169 | 177 | PF00786 | 0.361 |
LIG_LIR_Apic_2 | 154 | 158 | PF02991 | 0.361 |
LIG_LIR_Apic_2 | 395 | 400 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.168 |
LIG_LIR_Gen_1 | 74 | 83 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.168 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.340 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.418 |
LIG_Pex14_1 | 113 | 117 | PF04695 | 0.310 |
LIG_Pex14_1 | 402 | 406 | PF04695 | 0.325 |
LIG_Pex14_1 | 78 | 82 | PF04695 | 0.361 |
LIG_Pex14_2 | 117 | 121 | PF04695 | 0.381 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.408 |
LIG_Pex14_2 | 82 | 86 | PF04695 | 0.346 |
LIG_PTB_Apo_2 | 490 | 497 | PF02174 | 0.274 |
LIG_PTB_Apo_2 | 70 | 77 | PF02174 | 0.525 |
LIG_PTB_Apo_2 | 82 | 89 | PF02174 | 0.203 |
LIG_PTB_Phospho_1 | 490 | 496 | PF10480 | 0.290 |
LIG_PTB_Phospho_1 | 82 | 88 | PF10480 | 0.271 |
LIG_Rb_LxCxE_1 | 268 | 288 | PF01857 | 0.454 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.186 |
LIG_SH2_CRK | 616 | 620 | PF00017 | 0.286 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.274 |
LIG_SH2_GRB2like | 491 | 494 | PF00017 | 0.261 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.186 |
LIG_SH2_NCK_1 | 616 | 620 | PF00017 | 0.271 |
LIG_SH2_PTP2 | 437 | 440 | PF00017 | 0.310 |
LIG_SH2_PTP2 | 491 | 494 | PF00017 | 0.261 |
LIG_SH2_SRC | 491 | 494 | PF00017 | 0.261 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 386 | 390 | PF00017 | 0.274 |
LIG_SH2_STAT3 | 386 | 389 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.220 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.288 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.361 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.566 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.496 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 428 | 434 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 625 | 632 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 106 | 112 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 295 | 302 | PF11976 | 0.513 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.424 |
LIG_TRAF2_1 | 584 | 587 | PF00917 | 0.558 |
LIG_TYR_ITIM | 435 | 440 | PF00017 | 0.310 |
LIG_TYR_ITIM | 494 | 499 | PF00017 | 0.290 |
LIG_UBA3_1 | 248 | 256 | PF00899 | 0.308 |
LIG_WRC_WIRS_1 | 152 | 157 | PF05994 | 0.290 |
LIG_WRC_WIRS_1 | 189 | 194 | PF05994 | 0.403 |
MOD_CDC14_SPxK_1 | 253 | 256 | PF00782 | 0.361 |
MOD_CDK_SPK_2 | 250 | 255 | PF00069 | 0.308 |
MOD_CDK_SPxK_1 | 250 | 256 | PF00069 | 0.361 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.282 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.261 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.278 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.340 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.345 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.667 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.351 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.512 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.408 |
MOD_Cter_Amidation | 526 | 529 | PF01082 | 0.569 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.395 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.261 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.261 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.261 |
MOD_GlcNHglycan | 326 | 330 | PF01048 | 0.360 |
MOD_GlcNHglycan | 45 | 49 | PF01048 | 0.588 |
MOD_GlcNHglycan | 524 | 528 | PF01048 | 0.507 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.556 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.293 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.300 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.325 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.310 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.431 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.378 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.654 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.430 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.580 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.290 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.373 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.445 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.344 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.252 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.211 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.332 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.270 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.242 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.416 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.432 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.350 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.295 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.305 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.420 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.458 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.282 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.373 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.472 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.586 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.468 |
MOD_PIKK_1 | 581 | 587 | PF00454 | 0.292 |
MOD_PKA_1 | 500 | 506 | PF00069 | 0.374 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.294 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.261 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.378 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.366 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.445 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.350 |
MOD_Plk_2-3 | 295 | 301 | PF00069 | 0.340 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.300 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.313 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.278 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.151 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.256 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.298 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.153 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.369 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.155 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.280 |
MOD_Plk_4 | 631 | 637 | PF00069 | 0.423 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.375 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.404 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.249 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.379 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.373 |
MOD_SUMO_for_1 | 550 | 553 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 543 | 548 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_4 | 330 | 336 | PF01217 | 0.361 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.213 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.431 |
TRG_NLS_MonoExtC_3 | 536 | 542 | PF00514 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2N3 | Leptomonas seymouri | 50% | 88% |
A0A0S4IMH8 | Bodo saltans | 40% | 100% |
A0A1X0NL65 | Trypanosomatidae | 38% | 100% |
A0A1X0NM99 | Trypanosomatidae | 40% | 100% |
A0A3Q8IBB0 | Leishmania donovani | 92% | 100% |
A0A3R7MV96 | Trypanosoma rangeli | 40% | 100% |
A4HC54 | Leishmania braziliensis | 79% | 100% |
A4HT21 | Leishmania infantum | 91% | 100% |
C9ZTE5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AVI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q29611 | Canis lupus familiaris | 24% | 100% |
V5DU41 | Trypanosoma cruzi | 41% | 100% |