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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HB77
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0007165 | signal transduction | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0035556 | intracellular signal transduction | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0048015 | phosphatidylinositol-mediated signaling | 5 | 11 |
GO:0048017 | inositol lipid-mediated signaling | 4 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0006629 | lipid metabolic process | 3 | 4 |
GO:0006644 | phospholipid metabolic process | 4 | 4 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 4 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 4 |
GO:0008610 | lipid biosynthetic process | 4 | 4 |
GO:0008654 | phospholipid biosynthetic process | 5 | 4 |
GO:0009058 | biosynthetic process | 2 | 4 |
GO:0019637 | organophosphate metabolic process | 3 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044249 | cellular biosynthetic process | 3 | 4 |
GO:0044255 | cellular lipid metabolic process | 3 | 4 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 4 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 4 |
GO:0046486 | glycerolipid metabolic process | 4 | 4 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 4 |
GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090407 | organophosphate biosynthetic process | 4 | 4 |
GO:1901576 | organic substance biosynthetic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004430 | 1-phosphatidylinositol 4-kinase activity | 6 | 8 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 8 |
GO:0052742 | phosphatidylinositol kinase activity | 5 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.764 |
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.399 |
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.306 |
CLV_C14_Caspase3-7 | 590 | 594 | PF00656 | 0.381 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.529 |
CLV_PCSK_FUR_1 | 596 | 600 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.229 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 197 | 205 | PF00400 | 0.461 |
DOC_CKS1_1 | 545 | 550 | PF01111 | 0.361 |
DOC_CYCLIN_RxL_1 | 519 | 527 | PF00134 | 0.200 |
DOC_CYCLIN_RxL_1 | 582 | 593 | PF00134 | 0.254 |
DOC_CYCLIN_RxL_1 | 8 | 18 | PF00134 | 0.492 |
DOC_CYCLIN_yClb1_LxF_4 | 181 | 187 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 284 | 290 | PF00134 | 0.353 |
DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 462 | 471 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 533 | 542 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 158 | 166 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 361 | 369 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 473 | 482 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 81 | 89 | PF00069 | 0.362 |
DOC_PP1_RVXF_1 | 20 | 26 | PF00149 | 0.281 |
DOC_PP1_RVXF_1 | 86 | 92 | PF00149 | 0.347 |
DOC_PP2B_LxvP_1 | 268 | 271 | PF13499 | 0.310 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.312 |
DOC_SPAK_OSR1_1 | 274 | 278 | PF12202 | 0.541 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.406 |
DOC_USP7_MATH_2 | 145 | 151 | PF00917 | 0.461 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.354 |
LIG_14-3-3_CanoR_1 | 13 | 17 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 171 | 180 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.434 |
LIG_Actin_WH2_2 | 313 | 330 | PF00022 | 0.282 |
LIG_AP_GAE_1 | 146 | 152 | PF02883 | 0.452 |
LIG_APCC_ABBA_1 | 164 | 169 | PF00400 | 0.391 |
LIG_APCC_ABBAyCdc20_2 | 163 | 169 | PF00400 | 0.388 |
LIG_BIR_III_2 | 311 | 315 | PF00653 | 0.585 |
LIG_BRCT_BRCA1_1 | 496 | 500 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 514 | 518 | PF00533 | 0.308 |
LIG_Clathr_ClatBox_1 | 477 | 481 | PF01394 | 0.308 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.582 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.306 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.718 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.425 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.383 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.380 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.415 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.345 |
LIG_LIR_Gen_1 | 146 | 157 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 481 | 490 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 597 | 606 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 82 | 92 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.711 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 481 | 487 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 515 | 521 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.446 |
LIG_PCNA_yPIPBox_3 | 198 | 212 | PF02747 | 0.287 |
LIG_PCNA_yPIPBox_3 | 346 | 355 | PF02747 | 0.471 |
LIG_PCNA_yPIPBox_3 | 68 | 81 | PF02747 | 0.454 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.308 |
LIG_Pex14_2 | 482 | 486 | PF04695 | 0.380 |
LIG_Rb_pABgroove_1 | 35 | 43 | PF01858 | 0.510 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.341 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.327 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 452 | 456 | PF00017 | 0.313 |
LIG_SH2_PTP2 | 84 | 87 | PF00017 | 0.219 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 423 | 427 | PF00017 | 0.200 |
LIG_SH2_STAP1 | 526 | 530 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.460 |
LIG_SH2_STAT3 | 371 | 374 | PF00017 | 0.322 |
LIG_SH2_STAT3 | 457 | 460 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.436 |
LIG_SH3_2 | 287 | 292 | PF14604 | 0.396 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.510 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.314 |
LIG_SH3_CIN85_PxpxPR_1 | 287 | 292 | PF14604 | 0.396 |
LIG_SUMO_SIM_anti_2 | 505 | 511 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 537 | 544 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 399 | 409 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 537 | 544 | PF11976 | 0.282 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.411 |
LIG_TRAF2_1 | 47 | 50 | PF00917 | 0.414 |
LIG_TYR_ITIM | 248 | 253 | PF00017 | 0.452 |
LIG_TYR_ITIM | 524 | 529 | PF00017 | 0.419 |
LIG_UBA3_1 | 454 | 462 | PF00899 | 0.362 |
LIG_WRC_WIRS_1 | 96 | 101 | PF05994 | 0.587 |
LIG_WW_3 | 289 | 293 | PF00397 | 0.431 |
MOD_CDK_SPK_2 | 544 | 549 | PF00069 | 0.246 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.679 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.649 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.488 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.370 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.277 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.377 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.502 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.431 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.715 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.460 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.373 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.313 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.677 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.424 |
MOD_Cter_Amidation | 191 | 194 | PF01082 | 0.295 |
MOD_DYRK1A_RPxSP_1 | 292 | 296 | PF00069 | 0.475 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.741 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.565 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.304 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.479 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.666 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.676 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.420 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.495 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.289 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.524 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.474 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.513 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.488 |
MOD_LATS_1 | 113 | 119 | PF00433 | 0.459 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.389 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.492 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.537 |
MOD_N-GLC_2 | 346 | 348 | PF02516 | 0.258 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.403 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.458 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.312 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.327 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.334 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.413 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.612 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.452 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.353 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.526 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.308 |
MOD_PKA_1 | 414 | 420 | PF00069 | 0.492 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.462 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.442 |
MOD_PKB_1 | 276 | 284 | PF00069 | 0.429 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.564 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.475 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.420 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.261 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.419 |
MOD_Plk_2-3 | 147 | 153 | PF00069 | 0.552 |
MOD_Plk_2-3 | 256 | 262 | PF00069 | 0.421 |
MOD_Plk_2-3 | 406 | 412 | PF00069 | 0.380 |
MOD_Plk_2-3 | 573 | 579 | PF00069 | 0.417 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.595 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.355 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.419 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.632 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.382 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.355 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.167 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.463 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.345 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.720 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.467 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.514 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.308 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.358 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.219 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.484 |
TRG_NES_CRM1_1 | 50 | 64 | PF08389 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 14 | 18 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 522 | 527 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2J4 | Leptomonas seymouri | 71% | 97% |
A0A0S4JIN0 | Bodo saltans | 47% | 100% |
A0A1X0PA54 | Trypanosomatidae | 54% | 100% |
A0A3S7X8H7 | Leishmania donovani | 87% | 100% |
A0A422N5M8 | Trypanosoma rangeli | 51% | 100% |
A4IAC5 | Leishmania infantum | 87% | 100% |
A4IID4 | Xenopus tropicalis | 28% | 76% |
C9ZLW7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9B5E8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q2I5 | Leishmania major | 85% | 100% |
Q6GN16 | Xenopus laevis | 28% | 76% |