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:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HFS0
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006656 | phosphatidylcholine biosynthetic process | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0008654 | phospholipid biosynthetic process | 5 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046337 | phosphatidylethanolamine metabolic process | 6 | 1 |
GO:0046470 | phosphatidylcholine metabolic process | 4 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004103 | choline kinase activity | 5 | 5 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 5 |
GO:0004305 | ethanolamine kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.340 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.203 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.203 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.203 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.354 |
DOC_AGCK_PIF_2 | 319 | 324 | PF00069 | 0.395 |
DOC_CKS1_1 | 108 | 113 | PF01111 | 0.692 |
DOC_CYCLIN_RxL_1 | 587 | 599 | PF00134 | 0.322 |
DOC_MAPK_gen_1 | 481 | 491 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 627 | 636 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 627 | 636 | PF00069 | 0.272 |
DOC_PP1_RVXF_1 | 485 | 492 | PF00149 | 0.459 |
DOC_PP1_RVXF_1 | 568 | 575 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.402 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.658 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.388 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.532 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.276 |
LIG_14-3-3_CanoR_1 | 443 | 453 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 587 | 595 | PF00244 | 0.244 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.435 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.378 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.412 |
LIG_CtBP_PxDLS_1 | 68 | 72 | PF00389 | 0.529 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.507 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.718 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.286 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.390 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.419 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.456 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.514 |
LIG_LIR_Apic_2 | 326 | 332 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 330 | 340 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 415 | 422 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 604 | 613 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.317 |
LIG_LYPXL_yS_3 | 180 | 183 | PF13949 | 0.630 |
LIG_MYND_1 | 13 | 17 | PF01753 | 0.334 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.452 |
LIG_NRBOX | 590 | 596 | PF00104 | 0.375 |
LIG_PTB_Apo_2 | 266 | 273 | PF02174 | 0.405 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.337 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.395 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.407 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.502 |
LIG_SH2_SRC | 409 | 412 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.348 |
LIG_SH3_1 | 251 | 257 | PF00018 | 0.394 |
LIG_SH3_2 | 125 | 130 | PF14604 | 0.536 |
LIG_SH3_2 | 77 | 82 | PF14604 | 0.550 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.678 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.696 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.653 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.606 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.518 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.665 |
LIG_SUMO_SIM_anti_2 | 581 | 586 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 593 | 599 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.530 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.301 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.518 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.341 |
LIG_TYR_ITIM | 320 | 325 | PF00017 | 0.329 |
LIG_UBA3_1 | 410 | 416 | PF00899 | 0.502 |
MOD_CDK_SPxxK_3 | 338 | 345 | PF00069 | 0.271 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.520 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.724 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.703 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.540 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.479 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.352 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.656 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.594 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.635 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.303 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.541 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.330 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.449 |
MOD_CMANNOS | 603 | 606 | PF00535 | 0.310 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.632 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.417 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.361 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.259 |
MOD_GlcNHglycan | 509 | 513 | PF01048 | 0.203 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.384 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.466 |
MOD_GlcNHglycan | 637 | 641 | PF01048 | 0.362 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.667 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.703 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.707 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.642 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.670 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.639 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.436 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.583 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.480 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.504 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.444 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.531 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.537 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.499 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.346 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.681 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.340 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.560 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.502 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.499 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.575 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.467 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.289 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.355 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.529 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.577 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.667 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.546 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.256 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.690 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.599 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.497 |
MOD_PKA_1 | 434 | 440 | PF00069 | 0.468 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.523 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.438 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.352 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.340 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.487 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.383 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.547 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.508 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.256 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.499 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.349 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.297 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.525 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.449 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.336 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.591 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.406 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.502 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.502 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.373 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.725 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.586 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.269 |
TRG_DiLeu_BaEn_1 | 239 | 244 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_1 | 406 | 411 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C8 | Leptomonas seymouri | 55% | 100% |
A0A1X0P4H9 | Trypanosomatidae | 46% | 100% |
A0A3Q8IPY5 | Leishmania donovani | 74% | 100% |
A4I2U4 | Leishmania infantum | 74% | 100% |
E9ADC3 | Leishmania major | 73% | 100% |
E9AZ47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |