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: A0A3Q8IFG2
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 | 336 | 340 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.839 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.722 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.837 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.576 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.649 |
DOC_CKS1_1 | 526 | 531 | PF01111 | 0.471 |
DOC_CYCLIN_RxL_1 | 375 | 385 | PF00134 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 195 | 201 | PF00134 | 0.748 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.510 |
DOC_PP1_RVXF_1 | 376 | 383 | PF00149 | 0.439 |
DOC_PP1_RVXF_1 | 493 | 500 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.661 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.743 |
DOC_PP2B_LxvP_1 | 548 | 551 | PF13499 | 0.496 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 103 | 107 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.853 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.474 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 393 | 398 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 87 | 96 | PF00244 | 0.525 |
LIG_Actin_RPEL_3 | 572 | 591 | PF02755 | 0.454 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.788 |
LIG_BIR_III_4 | 222 | 226 | PF00653 | 0.732 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.633 |
LIG_CtBP_PxDLS_1 | 198 | 202 | PF00389 | 0.710 |
LIG_deltaCOP1_diTrp_1 | 40 | 47 | PF00928 | 0.692 |
LIG_eIF4E_1 | 430 | 436 | PF01652 | 0.579 |
LIG_EVH1_1 | 151 | 155 | PF00568 | 0.625 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.640 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.813 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.457 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.498 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.582 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.596 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.486 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.549 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.706 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.625 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.580 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.575 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.537 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.475 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 233 | 241 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 404 | 412 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 559 | 567 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 559 | 564 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 595 | 599 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.525 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.513 |
LIG_NRP_CendR_1 | 602 | 605 | PF00754 | 0.578 |
LIG_PALB2_WD40_1 | 416 | 424 | PF16756 | 0.584 |
LIG_PCNA_yPIPBox_3 | 271 | 283 | PF02747 | 0.735 |
LIG_PTB_Apo_2 | 278 | 285 | PF02174 | 0.714 |
LIG_PTB_Apo_2 | 530 | 537 | PF02174 | 0.462 |
LIG_PTB_Phospho_1 | 278 | 284 | PF10480 | 0.713 |
LIG_REV1ctd_RIR_1 | 533 | 541 | PF16727 | 0.458 |
LIG_SH2_GRB2like | 599 | 602 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.622 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.625 |
LIG_SH2_STAT3 | 244 | 247 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.550 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.621 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.730 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.542 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.479 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.477 |
LIG_SUMO_SIM_par_1 | 11 | 17 | PF11976 | 0.639 |
LIG_SUMO_SIM_par_1 | 498 | 504 | PF11976 | 0.433 |
LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.619 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.557 |
LIG_WRC_WIRS_1 | 20 | 25 | PF05994 | 0.638 |
LIG_WRC_WIRS_1 | 315 | 320 | PF05994 | 0.474 |
LIG_WW_3 | 289 | 293 | PF00397 | 0.504 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.800 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.699 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.738 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.616 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.703 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.458 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.460 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.721 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.762 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.587 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.504 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.542 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.486 |
MOD_Cter_Amidation | 174 | 177 | PF01082 | 0.624 |
MOD_DYRK1A_RPxSP_1 | 249 | 253 | PF00069 | 0.590 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.636 |
MOD_GlcNHglycan | 181 | 185 | PF01048 | 0.870 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.701 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.687 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.681 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.482 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.629 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.833 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.596 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.704 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.729 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.428 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.577 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.484 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.539 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.737 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.701 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.642 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.670 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.516 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.652 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.610 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.518 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.465 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.602 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.514 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.496 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.504 |
MOD_NEK2_2 | 470 | 475 | PF00069 | 0.543 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.633 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.650 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.650 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.444 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.539 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.504 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.492 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.458 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.480 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.569 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.573 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.646 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.459 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.476 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.677 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.390 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.465 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.480 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.519 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.445 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.628 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.853 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.786 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.682 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.478 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.472 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.467 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 481 | 486 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_1 | 559 | 564 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.573 |
TRG_DiLeu_LyEn_5 | 84 | 89 | PF01217 | 0.573 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 378 | 383 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.704 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC66 | Leptomonas seymouri | 69% | 96% |
A4HHJ3 | Leishmania braziliensis | 86% | 100% |
A4I4Q1 | Leishmania infantum | 99% | 100% |
E9AE54 | Leishmania major | 95% | 100% |
E9ALN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |