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:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IPY5
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
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 | 7 |
GO:0004103 | choline kinase activity | 5 | 5 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
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 | 0.576 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.274 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.292 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.681 |
DOC_AGCK_PIF_2 | 319 | 324 | PF00069 | 0.576 |
DOC_CDC14_PxL_1 | 507 | 515 | PF14671 | 0.476 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.778 |
DOC_CYCLIN_RxL_1 | 48 | 56 | PF00134 | 0.394 |
DOC_CYCLIN_RxL_1 | 584 | 596 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 481 | 491 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 485 | 492 | PF00149 | 0.492 |
DOC_PP1_RVXF_1 | 565 | 572 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.719 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.700 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.622 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.553 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.540 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 443 | 453 | PF00244 | 0.576 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.425 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.492 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.742 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.595 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.691 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.746 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.346 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.494 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.488 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.710 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.530 |
LIG_LIR_Apic_2 | 122 | 126 | PF02991 | 0.699 |
LIG_LIR_Apic_2 | 326 | 332 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 330 | 341 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 415 | 422 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 557 | 566 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 601 | 610 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 557 | 563 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 601 | 606 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.317 |
LIG_LYPXL_yS_3 | 180 | 183 | PF13949 | 0.630 |
LIG_LYPXL_yS_3 | 510 | 513 | PF13949 | 0.476 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.534 |
LIG_NRBOX | 587 | 593 | PF00104 | 0.370 |
LIG_PCNA_yPIPBox_3 | 16 | 24 | PF02747 | 0.432 |
LIG_PDZ_Class_3 | 634 | 639 | PF00595 | 0.568 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.494 |
LIG_PTAP_UEV_1 | 253 | 258 | PF05743 | 0.527 |
LIG_PTB_Apo_2 | 266 | 273 | PF02174 | 0.455 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.492 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.531 |
LIG_SH2_CRK | 620 | 624 | PF00017 | 0.292 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.492 |
LIG_SH2_SRC | 313 | 316 | PF00017 | 0.476 |
LIG_SH2_SRC | 324 | 327 | PF00017 | 0.476 |
LIG_SH2_SRC | 409 | 412 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 106 | 109 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.390 |
LIG_SH3_1 | 191 | 197 | PF00018 | 0.629 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.683 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.705 |
LIG_SUMO_SIM_par_1 | 590 | 596 | PF11976 | 0.356 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.619 |
LIG_TYR_ITIM | 178 | 183 | PF00017 | 0.582 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.492 |
LIG_TYR_ITIM | 320 | 325 | PF00017 | 0.492 |
LIG_TYR_ITIM | 618 | 623 | PF00017 | 0.297 |
LIG_UBA3_1 | 410 | 416 | PF00899 | 0.492 |
LIG_UBA3_1 | 452 | 460 | PF00899 | 0.476 |
LIG_WRC_WIRS_1 | 163 | 168 | PF05994 | 0.712 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.755 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.766 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.568 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.623 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.492 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.576 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.576 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.675 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.345 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.713 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.631 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.712 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.620 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.423 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.478 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.547 |
MOD_CMANNOS | 600 | 603 | PF00535 | 0.350 |
MOD_DYRK1A_RPxSP_1 | 247 | 251 | PF00069 | 0.675 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.768 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.553 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.478 |
MOD_GlcNHglycan | 277 | 283 | PF01048 | 0.295 |
MOD_GlcNHglycan | 335 | 339 | PF01048 | 0.251 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.423 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.376 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.292 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.353 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.556 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.767 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.765 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.665 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.738 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.546 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.619 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.685 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.438 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.511 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.498 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.519 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.492 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.648 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.731 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.548 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.626 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.771 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.679 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.492 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.500 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.492 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.489 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.555 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.445 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.434 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.733 |
MOD_OFUCOSY | 67 | 73 | PF10250 | 0.665 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.732 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.680 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.505 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.530 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.788 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.502 |
MOD_PKA_1 | 434 | 440 | PF00069 | 0.519 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.619 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.511 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.492 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.492 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.492 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.551 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.576 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.530 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.686 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.373 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.345 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.492 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.592 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.409 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.492 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.659 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.672 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.630 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.629 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.585 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.585 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.692 |
TRG_DiLeu_BaEn_1 | 406 | 411 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 628 | 631 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C8 | Leptomonas seymouri | 59% | 100% |
A4HFS0 | Leishmania braziliensis | 74% | 100% |
A4I2U4 | Leishmania infantum | 100% | 100% |
E9ADC3 | Leishmania major | 92% | 100% |
E9AZ47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |