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 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
Related structures:
AlphaFold database: E9ALN1
Term | Name | Level | Count |
---|---|---|---|
GO:0019220 | regulation of phosphate metabolic process | 6 | 7 |
GO:0019222 | regulation of metabolic process | 3 | 7 |
GO:0031323 | regulation of cellular metabolic process | 4 | 7 |
GO:0035303 | regulation of dephosphorylation | 7 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0030865 | cortical cytoskeleton organization | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 6 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.833 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.709 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.577 |
DEG_SPOP_SBC_1 | 152 | 156 | PF00917 | 0.495 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.649 |
DOC_CKS1_1 | 524 | 529 | PF01111 | 0.467 |
DOC_CYCLIN_RxL_1 | 373 | 383 | PF00134 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.761 |
DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 93 | 101 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 374 | 381 | PF00149 | 0.440 |
DOC_PP1_RVXF_1 | 491 | 498 | PF00149 | 0.442 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.653 |
DOC_PP2B_LxvP_1 | 194 | 197 | PF13499 | 0.759 |
DOC_PP2B_LxvP_1 | 546 | 549 | PF13499 | 0.504 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.375 |
DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.518 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.833 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 123 | 129 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 391 | 396 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 86 | 95 | PF00244 | 0.527 |
LIG_Actin_RPEL_3 | 570 | 589 | PF02755 | 0.453 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.790 |
LIG_BIR_III_4 | 220 | 224 | PF00653 | 0.745 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.619 |
LIG_deltaCOP1_diTrp_1 | 39 | 46 | PF00928 | 0.707 |
LIG_eIF4E_1 | 428 | 434 | PF01652 | 0.580 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.653 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.837 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.376 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.460 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.497 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.586 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.605 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.484 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.583 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.684 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.631 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.615 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.571 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.542 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.466 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 402 | 410 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 557 | 565 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 593 | 597 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.521 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.512 |
LIG_NRP_CendR_1 | 600 | 603 | PF00754 | 0.583 |
LIG_PALB2_WD40_1 | 414 | 422 | PF16756 | 0.584 |
LIG_PCNA_yPIPBox_3 | 269 | 281 | PF02747 | 0.741 |
LIG_PTB_Apo_2 | 276 | 283 | PF02174 | 0.724 |
LIG_PTB_Apo_2 | 528 | 535 | PF02174 | 0.466 |
LIG_PTB_Phospho_1 | 276 | 282 | PF10480 | 0.725 |
LIG_REV1ctd_RIR_1 | 531 | 539 | PF16727 | 0.462 |
LIG_SH2_GRB2like | 597 | 600 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.613 |
LIG_SH2_STAT3 | 242 | 245 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.551 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.740 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.622 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.482 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.476 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.475 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.653 |
LIG_SUMO_SIM_par_1 | 496 | 502 | PF11976 | 0.434 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.617 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.565 |
LIG_WRC_WIRS_1 | 19 | 24 | PF05994 | 0.644 |
LIG_WRC_WIRS_1 | 313 | 318 | PF05994 | 0.473 |
LIG_WW_3 | 287 | 291 | PF00397 | 0.500 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.806 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.701 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.773 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.725 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.702 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.459 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.465 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.706 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.591 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.507 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.548 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.477 |
MOD_DYRK1A_RPxSP_1 | 247 | 251 | PF00069 | 0.602 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.635 |
MOD_GlcNHglycan | 180 | 184 | PF01048 | 0.843 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.762 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.716 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.655 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.682 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.511 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.613 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.754 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.623 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.633 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.678 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.727 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.472 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.576 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.481 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.514 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.814 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.658 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.516 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.655 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.608 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.466 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.464 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.603 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.510 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.500 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.549 |
MOD_NEK2_2 | 468 | 473 | PF00069 | 0.542 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.647 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.654 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.448 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.540 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.507 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.492 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.461 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.481 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.571 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.579 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.682 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.608 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.459 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.475 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.673 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.390 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.469 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.481 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.491 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.448 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.617 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.834 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.640 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.811 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.695 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.476 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.469 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.470 |
MOD_SUMO_for_1 | 323 | 326 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 479 | 484 | PF01217 | 0.526 |
TRG_DiLeu_BaEn_1 | 557 | 562 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.577 |
TRG_DiLeu_LyEn_5 | 83 | 88 | PF01217 | 0.577 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 376 | 381 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.708 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC66 | Leptomonas seymouri | 68% | 96% |
A0A3Q8IFG2 | Leishmania donovani | 95% | 100% |
A4HHJ3 | Leishmania braziliensis | 86% | 100% |
A4I4Q1 | Leishmania infantum | 95% | 100% |
E9AE54 | Leishmania major | 94% | 100% |