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 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ADC3
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006644 | phospholipid metabolic process | 4 | 2 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 2 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 2 |
GO:0006656 | phosphatidylcholine biosynthetic process | 5 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0008654 | phospholipid biosynthetic process | 5 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 2 |
GO:0046337 | phosphatidylethanolamine metabolic process | 6 | 2 |
GO:0046470 | phosphatidylcholine metabolic process | 4 | 2 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090407 | organophosphate biosynthetic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004103 | choline kinase activity | 5 | 5 |
GO:0004305 | ethanolamine kinase activity | 5 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.326 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.539 |
DEG_SPOP_SBC_1 | 552 | 556 | PF00917 | 0.460 |
DOC_AGCK_PIF_2 | 319 | 324 | PF00069 | 0.479 |
DOC_CDC14_PxL_1 | 507 | 515 | PF14671 | 0.440 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.656 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.521 |
DOC_CYCLIN_RxL_1 | 587 | 599 | PF00134 | 0.321 |
DOC_MAPK_gen_1 | 481 | 491 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 485 | 492 | PF00149 | 0.452 |
DOC_PP1_RVXF_1 | 568 | 575 | PF00149 | 0.364 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.615 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.452 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.612 |
DOC_PP4_FxxP_1 | 200 | 203 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.428 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.468 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.420 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 131 | 139 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 230 | 237 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 443 | 453 | PF00244 | 0.479 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.363 |
LIG_BIR_III_2 | 140 | 144 | PF00653 | 0.537 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.452 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.694 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.681 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.711 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.331 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.474 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.449 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.601 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.457 |
LIG_LIR_Apic_2 | 122 | 126 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 198 | 203 | PF02991 | 0.494 |
LIG_LIR_Apic_2 | 326 | 332 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 149 | 158 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 330 | 341 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 415 | 422 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 436 | 445 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 604 | 613 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 626 | 631 | PF02991 | 0.322 |
LIG_LYPXL_yS_3 | 510 | 513 | PF13949 | 0.440 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.415 |
LIG_NRBOX | 590 | 596 | PF00104 | 0.315 |
LIG_PCNA_yPIPBox_3 | 16 | 24 | PF02747 | 0.335 |
LIG_PDZ_Class_3 | 637 | 642 | PF00595 | 0.464 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.401 |
LIG_PTAP_UEV_1 | 253 | 258 | PF05743 | 0.455 |
LIG_PTB_Apo_2 | 266 | 273 | PF02174 | 0.394 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.452 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.581 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.452 |
LIG_SH2_SRC | 313 | 316 | PF00017 | 0.440 |
LIG_SH2_SRC | 324 | 327 | PF00017 | 0.440 |
LIG_SH2_SRC | 409 | 412 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.343 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.611 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.579 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.635 |
LIG_SUMO_SIM_par_1 | 382 | 387 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 593 | 599 | PF11976 | 0.300 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.593 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.452 |
LIG_TYR_ITIM | 320 | 325 | PF00017 | 0.452 |
LIG_UBA3_1 | 410 | 416 | PF00899 | 0.452 |
LIG_UBA3_1 | 452 | 460 | PF00899 | 0.440 |
LIG_WRC_WIRS_1 | 163 | 168 | PF05994 | 0.602 |
LIG_WRC_WIRS_1 | 527 | 532 | PF05994 | 0.267 |
MOD_CDK_SPxK_1 | 77 | 83 | PF00069 | 0.551 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.553 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.612 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.607 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.560 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.462 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.479 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.479 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.545 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.289 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.649 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.557 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.601 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.538 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.411 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.441 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.507 |
MOD_CMANNOS | 603 | 606 | PF00535 | 0.296 |
MOD_DYRK1A_RPxSP_1 | 247 | 251 | PF00069 | 0.586 |
MOD_DYRK1A_RPxSP_1 | 77 | 81 | PF00069 | 0.543 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.701 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.505 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.422 |
MOD_GlcNHglycan | 277 | 283 | PF01048 | 0.400 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.279 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.252 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.428 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.726 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.629 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.585 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.668 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.519 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.587 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.545 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.689 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.333 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.438 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.458 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.452 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.497 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.668 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.501 |
MOD_N-GLC_2 | 170 | 172 | PF02516 | 0.536 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.633 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.662 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.452 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.459 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.326 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.452 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.455 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.514 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.315 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.683 |
MOD_OFUCOSY | 67 | 73 | PF10250 | 0.578 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.632 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.569 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.452 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.457 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.638 |
MOD_PKA_1 | 130 | 136 | PF00069 | 0.542 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.441 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.542 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.540 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.563 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.532 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.441 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.452 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.452 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.452 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.467 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.479 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.457 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.583 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.317 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.347 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.494 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.323 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.563 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.396 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.452 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.325 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.617 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.573 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.606 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.564 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.490 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.634 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.536 |
TRG_DiLeu_BaEn_1 | 406 | 411 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.370 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.359 |
TRG_NLS_MonoExtN_4 | 81 | 87 | PF00514 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C8 | Leptomonas seymouri | 58% | 100% |
A0A3Q8IPY5 | Leishmania donovani | 92% | 100% |
A4HFS0 | Leishmania braziliensis | 73% | 100% |
A4I2U4 | Leishmania infantum | 92% | 100% |
E9AZ47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |