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: E9AZ47
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:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0004103 | choline kinase activity | 5 | 4 |
GO:0004305 | ethanolamine kinase activity | 5 | 1 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 550 | 554 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 257 | 259 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 430 | 432 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.229 |
DOC_AGCK_PIF_2 | 315 | 320 | PF00069 | 0.529 |
DOC_CDC14_PxL_1 | 503 | 511 | PF14671 | 0.460 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.729 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.573 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.537 |
DOC_CYCLIN_RxL_1 | 583 | 595 | PF00134 | 0.356 |
DOC_MAPK_gen_1 | 477 | 487 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.365 |
DOC_PP1_RVXF_1 | 481 | 488 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 564 | 571 | PF00149 | 0.390 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.663 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.475 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.671 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.482 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.400 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.482 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 226 | 233 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 439 | 449 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.541 |
LIG_APCC_ABBA_1 | 268 | 273 | PF00400 | 0.393 |
LIG_BIR_III_2 | 140 | 144 | PF00653 | 0.593 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.520 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.475 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.734 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.648 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.697 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.319 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.480 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.485 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.538 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.640 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.495 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.461 |
LIG_LIR_Apic_2 | 122 | 126 | PF02991 | 0.670 |
LIG_LIR_Apic_2 | 64 | 70 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 322 | 333 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 411 | 418 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 600 | 609 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 505 | 509 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 600 | 605 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.315 |
LIG_LYPXL_yS_3 | 176 | 179 | PF13949 | 0.613 |
LIG_LYPXL_yS_3 | 506 | 509 | PF13949 | 0.460 |
LIG_NRBOX | 586 | 592 | PF00104 | 0.348 |
LIG_PCNA_yPIPBox_3 | 16 | 24 | PF02747 | 0.395 |
LIG_PDZ_Class_3 | 633 | 638 | PF00595 | 0.518 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.450 |
LIG_PTB_Apo_2 | 262 | 269 | PF02174 | 0.424 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.475 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.501 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 497 | 501 | PF00017 | 0.492 |
LIG_SH2_SRC | 309 | 312 | PF00017 | 0.460 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 513 | 517 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.374 |
LIG_SH3_1 | 190 | 196 | PF00018 | 0.587 |
LIG_SH3_2 | 78 | 83 | PF14604 | 0.586 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.693 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.614 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.599 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.616 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.581 |
LIG_SUMO_SIM_par_1 | 589 | 595 | PF11976 | 0.333 |
LIG_TYR_ITIM | 299 | 304 | PF00017 | 0.475 |
LIG_TYR_ITIM | 316 | 321 | PF00017 | 0.475 |
LIG_UBA3_1 | 406 | 412 | PF00899 | 0.475 |
LIG_UBA3_1 | 448 | 456 | PF00899 | 0.460 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.657 |
MOD_CDK_SPxK_1 | 77 | 83 | PF00069 | 0.583 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.583 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.597 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.662 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.475 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.529 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.529 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.405 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.627 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.321 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.717 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.549 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.639 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.395 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.493 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.528 |
MOD_CMANNOS | 599 | 602 | PF00535 | 0.326 |
MOD_DYRK1A_RPxSP_1 | 243 | 247 | PF00069 | 0.607 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.659 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.550 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.441 |
MOD_GlcNHglycan | 273 | 279 | PF01048 | 0.424 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.396 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.329 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.275 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.341 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.483 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.800 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.686 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.621 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.723 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.614 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.656 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.584 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.680 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.504 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.456 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.481 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.486 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.475 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.582 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.737 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.570 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.548 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.732 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.647 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.503 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.475 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.478 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.486 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.539 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.440 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.692 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.475 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.499 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.712 |
MOD_PKA_1 | 257 | 263 | PF00069 | 0.458 |
MOD_PKA_1 | 430 | 436 | PF00069 | 0.486 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.547 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.585 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.614 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.549 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.458 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.496 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.475 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.475 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.510 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.529 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.411 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.495 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.502 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.522 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.359 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.312 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.482 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.456 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.596 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.440 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.475 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.607 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.653 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.663 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.605 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.544 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.550 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.678 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.561 |
MOD_SUMO_rev_2 | 92 | 102 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_1 | 402 | 407 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 627 | 630 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 530 | 532 | PF00400 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C8 | Leptomonas seymouri | 57% | 100% |
A0A3Q8IPY5 | Leishmania donovani | 87% | 100% |
A4HFS0 | Leishmania braziliensis | 72% | 100% |
A4I2U4 | Leishmania infantum | 87% | 100% |
E9ADC3 | Leishmania major | 87% | 100% |