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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9ADA5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
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 | 7 |
GO:0019725 | cellular homeostasis | 2 | 7 |
GO:0030001 | metal ion transport | 6 | 2 |
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:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 7 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 7 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 7 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 7 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 7 |
GO:0022857 | transmembrane transporter activity | 2 | 7 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 7 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 7 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.311 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.336 |
DEG_SCF_FBW7_2 | 557 | 564 | PF00400 | 0.477 |
DOC_CYCLIN_RxL_1 | 267 | 277 | PF00134 | 0.551 |
DOC_CYCLIN_RxL_1 | 517 | 525 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 299 | 308 | PF00069 | 0.649 |
DOC_MAPK_gen_1 | 313 | 323 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 299 | 308 | PF00069 | 0.618 |
DOC_MAPK_MEF2A_6 | 313 | 321 | PF00069 | 0.407 |
DOC_MAPK_NFAT4_5 | 316 | 324 | PF00069 | 0.190 |
DOC_PP1_RVXF_1 | 268 | 275 | PF00149 | 0.591 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.262 |
DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.511 |
DOC_PP4_FxxP_1 | 410 | 413 | PF00568 | 0.281 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.319 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.648 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 66 | 75 | PF00244 | 0.404 |
LIG_Actin_WH2_2 | 278 | 296 | PF00022 | 0.557 |
LIG_APCC_ABBA_1 | 606 | 611 | PF00400 | 0.542 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.190 |
LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.228 |
LIG_EH1_1 | 203 | 211 | PF00400 | 0.307 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.240 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.434 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.218 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.271 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.230 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.437 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.551 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.333 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.657 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.574 |
LIG_LIR_Gen_1 | 252 | 259 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 28 | 38 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 345 | 352 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 417 | 427 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 544 | 555 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 252 | 256 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 544 | 550 | PF02991 | 0.432 |
LIG_NRBOX | 470 | 476 | PF00104 | 0.271 |
LIG_Pex14_1 | 32 | 36 | PF04695 | 0.271 |
LIG_PTB_Apo_2 | 600 | 607 | PF02174 | 0.520 |
LIG_SH2_PTP2 | 401 | 404 | PF00017 | 0.271 |
LIG_SH2_SRC | 467 | 470 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 529 | 533 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.224 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.571 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.490 |
LIG_Sin3_3 | 504 | 511 | PF02671 | 0.307 |
LIG_SUMO_SIM_anti_2 | 197 | 203 | PF11976 | 0.281 |
LIG_SUMO_SIM_anti_2 | 254 | 261 | PF11976 | 0.333 |
LIG_SUMO_SIM_anti_2 | 34 | 41 | PF11976 | 0.268 |
LIG_SUMO_SIM_anti_2 | 477 | 484 | PF11976 | 0.271 |
LIG_SUMO_SIM_anti_2 | 503 | 510 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 125 | 132 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 304 | 310 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 420 | 425 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 503 | 510 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 520 | 525 | PF11976 | 0.481 |
LIG_UBA3_1 | 184 | 191 | PF00899 | 0.521 |
LIG_Vh1_VBS_1 | 148 | 166 | PF01044 | 0.294 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.271 |
LIG_WRC_WIRS_1 | 39 | 44 | PF05994 | 0.271 |
LIG_WW_3 | 560 | 564 | PF00397 | 0.485 |
MOD_CDK_SPK_2 | 549 | 554 | PF00069 | 0.540 |
MOD_CDK_SPK_2 | 57 | 62 | PF00069 | 0.615 |
MOD_CDK_SPxK_1 | 557 | 563 | PF00069 | 0.479 |
MOD_CDK_SPxxK_3 | 57 | 64 | PF00069 | 0.610 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.281 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.615 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.271 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.487 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.424 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.237 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.280 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.323 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.619 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.333 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.436 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.249 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.270 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.271 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.271 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.355 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.372 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.318 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.247 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.665 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.617 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.436 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.296 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.578 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.486 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.373 |
MOD_N-GLC_1 | 531 | 536 | PF02516 | 0.286 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.388 |
MOD_N-GLC_1 | 602 | 607 | PF02516 | 0.302 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.444 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.259 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.273 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.349 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.354 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.726 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.163 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.370 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.333 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.589 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.271 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.240 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.471 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.160 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.437 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.271 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.437 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.510 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.538 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.274 |
MOD_OFUCOSY | 119 | 124 | PF10250 | 0.294 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.594 |
MOD_PKA_1 | 585 | 591 | PF00069 | 0.528 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.731 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.390 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.533 |
MOD_PKB_1 | 107 | 115 | PF00069 | 0.598 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.482 |
MOD_Plk_1 | 602 | 608 | PF00069 | 0.498 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.397 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.321 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.480 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.237 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.200 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.531 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.333 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.224 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.271 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.256 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.271 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.537 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.498 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.573 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.494 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.492 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.611 |
MOD_SUMO_rev_2 | 283 | 292 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 310 | 318 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 368 | 375 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_1 | 195 | 200 | PF01217 | 0.381 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.293 |
TRG_DiLeu_BaEn_1 | 417 | 422 | PF01217 | 0.237 |
TRG_DiLeu_BaEn_2 | 313 | 319 | PF01217 | 0.437 |
TRG_DiLeu_BaEn_3 | 300 | 306 | PF01217 | 0.590 |
TRG_DiLeu_BaLyEn_6 | 510 | 515 | PF01217 | 0.271 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.596 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.271 |
TRG_NLS_MonoExtC_3 | 583 | 589 | PF00514 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB11 | Leptomonas seymouri | 58% | 100% |
A0A3Q8IDA3 | Leishmania donovani | 90% | 100% |
A4HFQ2 | Leishmania braziliensis | 79% | 92% |
A4I2S7 | Leishmania infantum | 90% | 100% |
E9AZ30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q28CE7 | Xenopus tropicalis | 31% | 79% |