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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HFQ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 7 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 7 |
GO:0006882 | intracellular zinc ion homeostasis | 7 | 7 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019725 | cellular homeostasis | 2 | 7 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 7 |
GO:0042592 | homeostatic process | 3 | 7 |
GO:0046916 | obsolete intracellular transition metal ion homeostasis | 7 | 7 |
GO:0048878 | chemical homeostasis | 4 | 7 |
GO:0050801 | monoatomic ion homeostasis | 5 | 7 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 7 |
GO:0055069 | obsolete zinc ion homeostasis | 8 | 7 |
GO:0055076 | obsolete transition metal ion homeostasis | 8 | 7 |
GO:0055080 | monoatomic cation homeostasis | 6 | 7 |
GO:0055082 | intracellular chemical homeostasis | 3 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065008 | regulation of biological quality | 2 | 7 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 7 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 7 |
GO:0098771 | inorganic ion homeostasis | 6 | 7 |
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
GO:0030001 | metal ion transport | 6 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0000041 | transition metal ion transport | 7 | 1 |
GO:0006829 | zinc ion transport | 8 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0071577 | zinc ion transmembrane transport | 6 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 12 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 8 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 8 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 8 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 8 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.264 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.298 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.580 |
DOC_CYCLIN_RxL_1 | 319 | 330 | PF00134 | 0.520 |
DOC_CYCLIN_RxL_1 | 569 | 580 | PF00134 | 0.475 |
DOC_CYCLIN_RxL_1 | 588 | 596 | PF00134 | 0.507 |
DOC_MAPK_DCC_7 | 21 | 31 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 366 | 376 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 366 | 374 | PF00069 | 0.425 |
DOC_PP1_RVXF_1 | 320 | 327 | PF00149 | 0.607 |
DOC_PP1_RVXF_1 | 99 | 105 | PF00149 | 0.552 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.254 |
DOC_PP2B_LxvP_1 | 576 | 579 | PF13499 | 0.524 |
DOC_PP4_FxxP_1 | 463 | 466 | PF00568 | 0.265 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.329 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 583 | 592 | PF00244 | 0.477 |
LIG_APCC_ABBA_1 | 658 | 663 | PF00400 | 0.522 |
LIG_BIR_III_4 | 494 | 498 | PF00653 | 0.406 |
LIG_BRCT_BRCA1_1 | 397 | 401 | PF00533 | 0.251 |
LIG_CtBP_PxDLS_1 | 26 | 30 | PF00389 | 0.551 |
LIG_EH1_1 | 255 | 263 | PF00400 | 0.280 |
LIG_eIF4E_1 | 34 | 40 | PF01652 | 0.550 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.508 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.206 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.571 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.472 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.244 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.399 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.280 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.477 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.504 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.533 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.251 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.369 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.595 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.632 |
LIG_LIR_Gen_1 | 175 | 181 | PF02991 | 0.219 |
LIG_LIR_Gen_1 | 303 | 311 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 398 | 405 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 87 | 97 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 562 | 567 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.495 |
LIG_NRBOX | 193 | 199 | PF00104 | 0.212 |
LIG_NRBOX | 522 | 528 | PF00104 | 0.271 |
LIG_PCNA_yPIPBox_3 | 272 | 281 | PF02747 | 0.556 |
LIG_PCNA_yPIPBox_3 | 349 | 362 | PF02747 | 0.534 |
LIG_Pex14_1 | 85 | 89 | PF04695 | 0.271 |
LIG_REV1ctd_RIR_1 | 93 | 99 | PF16727 | 0.211 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.211 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.212 |
LIG_SH2_PTP2 | 454 | 457 | PF00017 | 0.271 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.549 |
LIG_SH2_SRC | 519 | 522 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.212 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.564 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.505 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.425 |
LIG_Sin3_3 | 556 | 563 | PF02671 | 0.280 |
LIG_SUMO_SIM_anti_2 | 175 | 184 | PF11976 | 0.212 |
LIG_SUMO_SIM_anti_2 | 249 | 255 | PF11976 | 0.265 |
LIG_SUMO_SIM_anti_2 | 28 | 33 | PF11976 | 0.548 |
LIG_SUMO_SIM_anti_2 | 306 | 313 | PF11976 | 0.310 |
LIG_SUMO_SIM_anti_2 | 36 | 42 | PF11976 | 0.547 |
LIG_SUMO_SIM_anti_2 | 377 | 382 | PF11976 | 0.243 |
LIG_SUMO_SIM_anti_2 | 529 | 537 | PF11976 | 0.271 |
LIG_SUMO_SIM_anti_2 | 555 | 562 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 175 | 184 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 356 | 363 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 36 | 42 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 377 | 384 | PF11976 | 0.212 |
LIG_SUMO_SIM_par_1 | 473 | 478 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 555 | 562 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 572 | 577 | PF11976 | 0.470 |
LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.305 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.550 |
LIG_UBA3_1 | 236 | 243 | PF00899 | 0.433 |
LIG_WRC_WIRS_1 | 277 | 282 | PF05994 | 0.406 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.271 |
LIG_WRC_WIRS_1 | 92 | 97 | PF05994 | 0.271 |
MOD_CDK_SPK_2 | 601 | 606 | PF00069 | 0.527 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.572 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.424 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.295 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.644 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.570 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.271 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.526 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.265 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.212 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.357 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.506 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.287 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.250 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.366 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.324 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.271 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.269 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.305 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.410 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.237 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.271 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.271 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.352 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.437 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.245 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.576 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.619 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.617 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.425 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.617 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.365 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.543 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.563 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.271 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.565 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.593 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.357 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.552 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.336 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.308 |
MOD_N-GLC_1 | 627 | 632 | PF02516 | 0.367 |
MOD_N-GLC_1 | 654 | 659 | PF02516 | 0.312 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.573 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.273 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.605 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.340 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.294 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.578 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.294 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.596 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.274 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.565 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.274 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.294 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.279 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.286 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.477 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.544 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.461 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.466 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.262 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.447 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.376 |
MOD_NEK2_2 | 91 | 96 | PF00069 | 0.212 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.555 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.558 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.614 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.390 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.572 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.206 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.618 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.600 |
MOD_Plk_1 | 615 | 621 | PF00069 | 0.496 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.508 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.298 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.321 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.550 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.435 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.359 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.594 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.583 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.329 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.367 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.295 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.290 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.508 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.248 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.271 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.570 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.508 |
MOD_SUMO_rev_2 | 363 | 371 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 421 | 428 | PF00179 | 0.448 |
TRG_DiLeu_BaEn_1 | 115 | 120 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_1 | 247 | 252 | PF01217 | 0.382 |
TRG_DiLeu_BaEn_1 | 306 | 311 | PF01217 | 0.271 |
TRG_DiLeu_BaEn_1 | 470 | 475 | PF01217 | 0.248 |
TRG_DiLeu_BaEn_2 | 366 | 372 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 562 | 567 | PF01217 | 0.271 |
TRG_DiLeu_LyEn_5 | 115 | 120 | PF01217 | 0.559 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.211 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.271 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 591 | 595 | PF00026 | 0.269 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB11 | Leptomonas seymouri | 55% | 100% |
A0A3Q8IDA3 | Leishmania donovani | 78% | 100% |
A0A3Q8IGB8 | Leishmania donovani | 23% | 100% |
A4HJM3 | Leishmania braziliensis | 24% | 100% |
A4I2S7 | Leishmania infantum | 77% | 100% |
A4I745 | Leishmania infantum | 24% | 100% |
E9ADA5 | Leishmania major | 79% | 100% |
E9AZ30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9B239 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q622 | Leishmania major | 24% | 100% |