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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
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 |
Related structures:
AlphaFold database: E9AZ30
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 | 7 |
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 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0030001 | metal ion transport | 6 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 8 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 7 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 8 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 8 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 7 |
GO:0022857 | transmembrane transporter activity | 2 | 8 |
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 | 272 | 276 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.322 |
CLV_PCSK_FUR_1 | 106 | 110 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.328 |
DEG_SCF_FBW7_2 | 556 | 563 | PF00400 | 0.496 |
DOC_CYCLIN_RxL_1 | 266 | 277 | PF00134 | 0.521 |
DOC_CYCLIN_RxL_1 | 45 | 52 | PF00134 | 0.552 |
DOC_CYCLIN_RxL_1 | 516 | 524 | PF00134 | 0.469 |
DOC_MAPK_gen_1 | 312 | 322 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 61 | 69 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 312 | 320 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 267 | 274 | PF00149 | 0.489 |
DOC_PP2B_LxvP_1 | 523 | 526 | PF13499 | 0.527 |
DOC_PP4_FxxP_1 | 409 | 412 | PF00568 | 0.266 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.320 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 137 | 141 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 65 | 70 | PF00244 | 0.402 |
LIG_APCC_ABBA_1 | 605 | 610 | PF00400 | 0.523 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.197 |
LIG_BRCT_BRCA1_1 | 343 | 347 | PF00533 | 0.250 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.680 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.471 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.219 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.250 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.228 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.281 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.340 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.353 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.471 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.499 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.532 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.299 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.627 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.582 |
LIG_LIR_Gen_1 | 251 | 258 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 34 | 44 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 344 | 351 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 416 | 426 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 5 | 14 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 509 | 514 | PF02991 | 0.289 |
LIG_NRBOX | 469 | 475 | PF00104 | 0.271 |
LIG_Pex14_1 | 32 | 36 | PF04695 | 0.271 |
LIG_Pex14_2 | 3 | 7 | PF04695 | 0.201 |
LIG_PTB_Apo_2 | 599 | 606 | PF02174 | 0.512 |
LIG_SH2_PTP2 | 400 | 403 | PF00017 | 0.271 |
LIG_SH2_SRC | 466 | 469 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 532 | 536 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.564 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.197 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.505 |
LIG_SUMO_SIM_anti_2 | 196 | 202 | PF11976 | 0.266 |
LIG_SUMO_SIM_anti_2 | 253 | 260 | PF11976 | 0.310 |
LIG_SUMO_SIM_anti_2 | 323 | 328 | PF11976 | 0.238 |
LIG_SUMO_SIM_anti_2 | 476 | 483 | PF11976 | 0.271 |
LIG_SUMO_SIM_anti_2 | 502 | 509 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 124 | 131 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 303 | 309 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 419 | 424 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 502 | 509 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 519 | 524 | PF11976 | 0.463 |
LIG_Vh1_VBS_1 | 147 | 165 | PF01044 | 0.274 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.271 |
LIG_WRC_WIRS_1 | 39 | 44 | PF05994 | 0.271 |
LIG_WW_3 | 559 | 563 | PF00397 | 0.503 |
MOD_CDK_SPK_2 | 548 | 553 | PF00069 | 0.532 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.611 |
MOD_CDK_SPxK_1 | 556 | 562 | PF00069 | 0.496 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.606 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.565 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.422 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.296 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.266 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.648 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.253 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.271 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.506 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.458 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.244 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.271 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.271 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.386 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.271 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.623 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.311 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.275 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.271 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.271 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.357 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.425 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.250 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.653 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.589 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.654 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.239 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.491 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.271 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.569 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.582 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.611 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.311 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.372 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.308 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.262 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.277 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.342 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.299 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.571 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.382 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.299 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.573 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.605 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.275 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.275 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.299 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.279 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.601 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.282 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.471 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.544 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.454 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.276 |
MOD_OFUCOSY | 118 | 123 | PF10250 | 0.274 |
MOD_PK_1 | 65 | 71 | PF00069 | 0.201 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.587 |
MOD_PKA_1 | 584 | 590 | PF00069 | 0.520 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.625 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.337 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.397 |
MOD_PKB_1 | 106 | 114 | PF00069 | 0.604 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.503 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.618 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.496 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.504 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.563 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.303 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.359 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.323 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.390 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.397 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.433 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.362 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.246 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.561 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.396 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.341 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.336 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.271 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.281 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.285 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.528 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.504 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.649 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.509 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.506 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.624 |
MOD_SUMO_rev_2 | 309 | 317 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 367 | 374 | PF00179 | 0.446 |
TRG_DiLeu_BaEn_1 | 194 | 199 | PF01217 | 0.392 |
TRG_DiLeu_BaEn_1 | 253 | 258 | PF01217 | 0.271 |
TRG_DiLeu_BaEn_1 | 416 | 421 | PF01217 | 0.246 |
TRG_DiLeu_BaEn_2 | 312 | 318 | PF01217 | 0.446 |
TRG_DiLeu_BaEn_3 | 299 | 305 | PF01217 | 0.593 |
TRG_DiLeu_BaLyEn_6 | 509 | 514 | PF01217 | 0.271 |
TRG_DiLeu_BaLyEn_6 | 62 | 67 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.271 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.606 |
TRG_NES_CRM1_1 | 599 | 610 | PF08389 | 0.459 |
TRG_NLS_MonoExtC_3 | 582 | 588 | PF00514 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB11 | Leptomonas seymouri | 59% | 100% |
A0A3Q8IDA3 | Leishmania donovani | 91% | 100% |
A4HFQ2 | Leishmania braziliensis | 78% | 100% |
A4HJM3 | Leishmania braziliensis | 25% | 100% |
A4I2S7 | Leishmania infantum | 90% | 100% |
E9ADA5 | Leishmania major | 89% | 100% |